Literature DB >> 31762949

Do early interventions prevent PTSD? A systematic review and meta-analysis of the safety and efficacy of early interventions after sexual assault.

Veerle Oosterbaan1, Milou L V Covers1, Iva A E Bicanic1, Rafaële J C Huntjens2, Ad de Jongh3,4,5,6.   

Abstract

Objective: To review the safety and efficacy of early interventions after sexual assault in reducing or preventing posttraumatic stress disorder (PTSD). Method: Systematic searches were performed on studies (1980-2018) that examined the efficacy of interventions for PTSD within 3 months after sexual assault.
Results: The review identified 7 studies (n = 350) with high risk of bias that investigated 5 interventions. Only two studies reported on safety. Contact with the authors of six studies provided no indications for the occurrence of adverse events. Two studies reported the efficacy using PTSD diagnosis as dependent variable but found no difference between groups. All studies reported on efficacy using PTSD severity as dependent variable. For the meta-analysis, 4 studies (n = 293) were included yielding significantly greater reductions of PTSD severity than standard care at 2 to 12 months follow-up (g = -0.23, 95% CI [-0.46, 0.00]), but not at 1 to 6 weeks post-intervention (g = -0.28, 95% CI [-0.57, 0.02]). The heterogeneity of the interventions precluded further analyses. Discussion: Findings suggest that early interventions can lead to durable effects on PTSD severity after sexual assault. However, due to limited availability of data, it is impossible to draw definite conclusions about safety and efficacy of early interventions, and their potential to prevent PTSD.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Sexual assault; early intervention; meta-analysis; posttraumatic stress disorder; prevention; safety; • Seven studies have investigated early interventions post-rape.• The studies have a highly diverse design and a high risk of bias.• There is little data on safety and the prevention of posttraumatic stress disorder.• Early intervention can potentially reduce the severity of posttraumatic stress disorder.

Year:  2019        PMID: 31762949      PMCID: PMC6853210          DOI: 10.1080/20008198.2019.1682932

Source DB:  PubMed          Journal:  Eur J Psychotraumatol        ISSN: 2000-8066


Sexual assault or rape is a highly common trauma with an estimated lifetime prevalence of up to 10% (Benjet et al., 2016; FRA (European Union Agency for Fundamental Rights), 2015; Kessler, Sonnega, Bromet, Hughes, & Nelson, 1995). In the aftermath of sexual assault 30–50% of rape victims develop posttraumatic stress disorder (PTSD; e.g. Elklit & Christiansen, 2010; Kessler et al., 1995; Möller, Bäckström, Söndergaard, & Helström, 2014; Rothbaum, Foa, Riggs, Murdock, & Walsh, 1992; Steenkamp, Dickstein, Salters-Pedneault, Hofmann, & Litz, 2012; Zinzow et al., 2012), with a mean duration of 9 years and 2 months (Kessler et al., 2017). PTSD has marked consequences on victims’ social, interpersonal, and occupational functioning (Perilloux, Duntley, & Buss, 2012). Given the high prevalence of sexual assault and its severe and long-lasting consequences, there is a great need for effective interventions after sexual assault. An important issue that arises in developing and implementing such interventions is their timing. PTSD symptoms usually stabilize at 3-months post-trauma (American Psychiatric Association [APA], 2013). As such, late intervention can be defined as any treatment applied 3 months or more post-trauma. The effectiveness of late interventions is well documented by systematic reviews (Regehr, Alaggia, Dennis, Pitts, & Saini, 2013; Vickerman & Margolin, 2009) and these are integrated into international treatment guidelines (APA, 2017; International Society for Traumatic Stress Studies Guidelines Committee [ISTSS], 2018; National Health and Medical Research Council [NHMRC], 2013; National Institute for Health and Care Excellence [NICE], 2018; World Health Organization [WHO], 2013, 2017). Nonetheless, these interventions are not effective for all victims of sexual assault. In a systematic review of rape intervention research, Vickerman and Margolin (2009) reported that in all these intervention studies at least one-third of victims remained symptomatic at post-treatment follow-up. As such, it seems important to develop early interventions, defined as interventions within 3 months after the sexual assault, aimed at preventing PTSD. As a matter of fact, there are solid arguments in favour of early interventions. Foremost, availability of effective early interventions could reduce the significant portion of sexual assault victims that currently goes on to develop PTSD and is burdened for many years after. Prevention of PTSD could also reduce the risk of comorbid problems such as substance dependence, depression, anxiety, and suicidality (Galatzer-Levy, Nickerson, Litz, & Marmar, 2013). A second argument in favour of early intervention is economics. Sexual assault is a notable economic burden for society. For example, the cost of adult rape victims in the USA in 2014 was more than 3.1 trillion dollars, allocating more than 2 trillion dollars to the costs of victims’ mental health problems (Peterson, DeGue, Florence, & Lokey, 2017). Thus, early intervention might reduce these costs. A third argument concerns the access to victims. The early stages after sexual assault provide unique access to these victims when they contact rape crisis centres, present themselves at hospitals for forensic examinations, or receive medical care for physical injuries and/or preventative measures for sexually transmitted diseases and pregnancy (Miller, Cranston, Davis, Newman, & Resnick, 2015; Price, Davidson, Ruggiero, Acierno, & Resnick, 2014). Hence, early intervention in a multidisciplinary setting can reach the many victims who otherwise do not seek help for the psychological sequelae of sexual assault until years later (Ahrens, Campbell, Ternier-Thames, Wasco, & Sefl, 2007; Ullman, 2007; Walsh, Banyard, Moynihan, Ward, & Cohn, 2010). In line with these arguments, international treatment guidelines on PTSD also recommend intervention for those with severe posttraumatic stress symptoms, as well as psychological monitoring for those with mild posttraumatic stress symptoms immediately post-trauma (APA, 2017; ISTSS, 2018; NHMRC, 2013; NICE, 2018; WHO, 2013, 2017). The most recent treatment guidelines further acknowledge that there is emerging evidence for the prevention of PTSD with single session EMDR therapy, debriefing supplemented with cohesion training exercises, brief dyadic therapy and self-guided internet-based interventions (ISTSS, 2018). Nevertheless, these guidelines acknowledge that the level of evidence for these recommendations is low. One meta-analysis that examined the efficacy of early intervention in victims of varied forms of trauma found that the effectiveness of early intervention is not superior to no intervention in reducing PTSD symptoms, nor in preventing the development of PTSD (Roberts, Kitchiner, Kenardy, & Bisson, 2009). However, these findings may not be applicable to sexual assault victims, as they comprise a subset of trauma victims who are at the highest risk of developing PTSD. In fact, the World Mental Health Surveys reported that 30% of rape victims developed PTSD compared to 4% of all trauma-exposed individuals (Kessler et al., 2017). Dworkin and Schumacher (2016) conducted a systematic review of post-rape help-seeking behaviour and posttraumatic stress and reported that some studies suggest that early psychological intervention could reduce the risk of posttraumatic stress. It is important to note that to date, no meta-analysis or (systematic) review has been conducted on the safety and efficacy of data specifically pertaining to early interventions after sexual trauma. The cause of this lack of research may lie in a number of arguments that have been raised against the application of early interventions. Firstly, posttraumatic stress symptoms are likely to regress naturally during the first 3 months after sexual assault. For example, up to 94% meets the criteria (aside from the criterion of symptom duration) for a PTSD diagnosis 1 week following sexual assault, while only 45–48% meets these criteria after 3 months (Elklit & Christiansen, 2010; Rothbaum et al., 1992; Steenkamp et al., 2012). Secondly, mental health treatments are time-intensive as well as expensive whereas mental health professionals are scarce. Therefore, some scholars regard it an unnecessary use of valuable resources to intervene at an earlier stage (McNally, Bryant, & Ehlers, 2003), and recommend that interventions should be postponed until PTSD has developed and can be determined. Thirdly, and probably most important, meta-analyses of controlled studies on the effectiveness of psychological debriefing immediately post-trauma have found the use of early intervention ineffective or even harmful (Rose, Bisson, Churchill, & Wessely, 2002; Van Emmerik, Kamphuis, Hulsbosch, & Emmelkamp, 2002), resulting in debate about the safety of early interventions (Litz, Gray, Bryant, & Adler, 2006). Examining the impact of early interventions on PTSD is important for the development of treatment directives and clinical decision-making. To determine whether early interventions after sexual assault – other than psychological debriefing – should be implemented, we conducted a systematic literature review and meta-analyses to synthesize the existing evidence on early interventions after sexual assault and to determine their safety, efficacy in preventing PTSD. It was hypothesized that early intervention would be safe and efficacious in preventing PTSD and reducing PTSD symptom severity.

Methods

This systematic literature review is conducted according to the guidelines of the Cochrane Handbook for Systematic Reviews of Interventions (Higgins & Green, 2011) and reported following the PRISMA Statement (Liberati et al., 2009).

Criteria for the selection of studies

Types of studies

For the current review, any type of intervention study was eligible. Both randomized and non-randomized trials were considered. Studies had to be reported in English or Dutch.

Types of participants

The studies should include participants that experienced a sexual trauma within 3 months prior to the intervention. Sexual trauma was defined as any type of nonconsensual sexual activity including oral, vaginal or anal penetration or any other type of sexual assault. Three months were chosen as a timeframe for an early intervention because PTSD symptoms usually begin within that timeframe (APA, 2013). Studies were also excluded if participants were younger than 16 years old because trauma responses including PTSD are expressed differently in children (APA, 2013).

Types of intervention

Any type of intervention aimed at treating or preventing posttraumatic stress was eligible with the exception of psychological debriefing. Psychological debriefing was excluded because it has been found detrimental to the treatment of sexual assault victims as evidenced by Rose et al. (2002) in a Cochrane review on psychological debriefing for preventing PTSD.

Types of outcome

Finally, studies were eligible for inclusion if they measured the outcome of the intervention in terms of PTSD symptom decrease or meeting the criteria of a PTSD diagnosis. This could be either a primary or secondary outcome measure of the study and could be reported as any statistical parameter.

Search methods for identification of studies

For this literature review, systematic searches were performed of the following databases: MEDLINE, Embase, CINAHL, PsycINFO, the Social Sciences Citation Index and the Cochrane database. The full search strategies for each database can be found in Appendix A. Boolean operators were used to create search strings searching for studies about sexual trauma, intervention or prevention, and PTSD. Each search string included a concept to exclude studies targeting children or childhood sexual abuse, using the search term ‘child*’. The search strings were limited to include records published from 1 January 1980 because PTSD did not exist as a diagnosis in the Diagnostic and Statistical Manual of Mental Disorders (DSM) before 1980 (APA, 1968). The search was executed on 30 April 2018. Meta-analyses and systematic reviews were only excluded at the full-text assessment stage. Additionally, the references listed in all included studies were reviewed as well as the articles listed as citing the included studies in Google Scholar.

Data collection and analysis

Methods for the selection of studies

The search results from the different databases were merged in Rayyan, a website for systematic reviews (Ouzzani, Hammady, Fedorowicz, & Elmagarmid, 2016), and duplicate records were removed. The first two review authors independently screened titles and abstracts of the remaining records to identify those that needed to be examined in full-text. This resulted in 2.9% disagreement between authors, which was resolved by discussion. Both authors also independently assessed the full-text reports on the eligibility criteria. The 4% disagreement was solved by discussion and usually stemmed from inaccuracy from either one of the authors.

Data extraction and management

Both authors independently extracted the relevant data from the included studies which pertained to details of the studies’ setting, eligibility criteria, procedure of randomization and blinding, participant characteristics, outcome measures, follow-up, results, analysis, drop-out rates, reasons for drop-out, (serious) adverse events, and main conclusion and topics of discussion. Minor disagreements about randomization and drop-out rates were solved by discussion.

Data analysis

For each study, the first two review authors independently assessed the risk of bias using the Cochrane tool of Bias. A qualitative synthesis was conducted by comparing the included studies on the extracted data. Two meta-analyses were conducted to analyse the effect of early intervention compared to standard care on PTSD symptom severity at first post-treatment assessment and longest follow-up. Because the studies utilized different instruments to measure PTSD, the standardized mean differences (i.e., Hedges’ g) were calculated. Due to clinical heterogeneity in interventions, measures and timing of measurements, random effects models were chosen. Resnick et al. (2007) and Miller et al. (2015) reported means and standard deviations separately for victims with and without prior rape history. However, prior rape history was not of interest for the present study. Therefore, the means and standard deviations in the intervention and control groups of all rape victims were calculated by pooling the standard deviations and means of those with and without prior rape history. Review Manager (2014) was used to conduct the meta-analyses and to produce the forest plots as well as the summary graph of the risk of bias.

Results

Results of the search

Figure 1 depicts a flowchart of the search process. Ultimately, seven studies reported in nine records met the eligibility criteria and were included in the qualitative synthesis presented in this review. The study reported by Resnick et al. (2007) was preliminarily reported by Resnick, Acierno, Holmes, Kilpatrick, and Jager (1999) and Resnick, Acierno, Kilpatrick, and Holmes (2005). Because the longest follow-up of the largest population is reported in Resnick et al. (2007), this record was used in the qualitative synthesis of this review.
Figure 1.

Flow diagram of the study selection process. PTSD = Posttraumatic stress disorder. Adapted from ‘preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement’ (Moher, Liberati, Tetzlaff, Altman, & the PRISMA group, 2009).

Flow diagram of the study selection process. PTSD = Posttraumatic stress disorder. Adapted from ‘preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement’ (Moher, Liberati, Tetzlaff, Altman, & the PRISMA group, 2009).

Included studies

The seven included studies were all reported in English. Table 1 shows an overview of the characteristics of these studies.
Table 1.

Characteristics of included studies.

CitationCountrySettingN in analysisParticipant characteristicsMain inclusion criteriaMain exclusion criteriaInterventionsSessions
Echeburúaet al. (1996)SpainSeeking treatment at psychological counselling centres20FemalesAge: 22 yrsSD = 6.9Sexual aggression < 3 monthsMeeting DSM-III-R criteria for PTSDSevere mental illnessSevere physical illnessCognitive restructuring, coping skills training and progressive muscular relaxation training vs. progressive muscular relaxation training5 weekly60-minute sessions
Resnicket al. (2007)USASeeking forensic examination at an academic medical centre140FemalesAge: 26.1 yrsSD = 9.8Sexual assault < 72 hoursSevere mental illnessSevere physical illnessIntoxicationIntellectual disabilityPre-examination video intervention vs. standard careSingle17-minute video
Rothbaumet al. (2012)USAPublic hospital emergency department4765% femalesAge: 31.5 yrsSD NRTrauma < 72 hoursIntoxicationNo memory of eventModified prolonged exposure session vs. standard care3 weekly60-minute sessions
Tarquinio et al. (2012a)FranceVia research centre, family doctor or regional victim aid associations17aFemalesAge: 32.2 yrsSD = 9.1Sexual trauma 24–72 hours agoFirst timeFiled police complaintSevere mental illnessSevere physical illnessIntoxicationIntellectual disabilityNewly integrated EMDR protocolSingle113-minute session
Tarquinio et al. (2012b)FranceReferral via psychologists of regional victim aid associations6aFemalesAge: 33.8 yrsSD = 7.4Sexual assault 8–12 weeks agoBy intimate partnerFiled police complaintNo previous similar traumaSevere mental illnessSevere physical illnessIntoxicationIntellectual disabilityStandard EMDR treatment protocol according to Shapiro (2001)3–4 weekly60-minute sessions
Milleret al. (2015)USAVia specialized nurse examiners at local hospital69–74bFemalesAge: 28.8 yrsSD = 10.5Sexual assault < 72 hoursSevere mental illnessSevere physical illnessIntoxicationIntellectual disabilityNo memory of eventPostexamination video intervention + standard care vs. standard careSingle9-minute video
Nixonet al. (2016)AustraliaSeeking treatment at a rape and sexual assault crisis centre46cFemalesAge: 31.3 yrsSD = NRRape or sexual assault < 1 monthMeeting criteria for ASDSevere mental illnessIntoxicationIntellectual disabilityCognitive processing therapy vs. standard care6 weekly90-minute sessions

SD = standard deviation, NR = not reported, vs. = versus, DSM-III-R = Diagnostic and Statistical Manual of Mental Disorders third edition revised, ASD = acute stress disorder. a Initial sample size and drop-out rates not reported. b Depending on follow up. c Using multiple imputation by chained equations.

Characteristics of included studies. SD = standard deviation, NR = not reported, vs. = versus, DSM-III-R = Diagnostic and Statistical Manual of Mental Disorders third edition revised, ASD = acute stress disorder. a Initial sample size and drop-out rates not reported. b Depending on follow up. c Using multiple imputation by chained equations.

Setting

The studies were conducted in high-income countries, generally among individuals seeking medical, forensic or psychological care/examination.

Participants

The studies exclusively included sexual assault victims, except for Rothbaum et al. (2012), who recruited all participants presenting at a hospital emergency department but reported results of rape victims separately. Sexual assault was generally not further defined, meaning it could include, but was not limited to, unwanted oral, anal, or vaginal penetration. The inclusion period ranged from 72 h through 3 months after the assault. The majority of the participants was female. The mean age of the participants in the various studies ranged from 22 years to 33.8 years.

Intervention

The seven studies investigated a multitude of different interventions (Table 1). On average, participants received three-and-a-half sessions in the active trial phase. Two studies of the same research group investigated the addition of a video intervention to a forensic examination. Immediately preceding the forensic examination, Resnick et al. (2007) showed participants a video that was designed to reduce distress during the forensic examination and provide psychoeducation on coping strategies and substance abuse prevention. Using only the psychoeducational and coping strategies components of the video used in the study of Resnick et al. (2007), Miller et al. (2015) showed participants in their intervention group the adapted video immediately after forensic examination.

Control

Four of the seven studies contained a control group in which the participants received standard care. The standard care in the two video intervention studies (Miller et al., 2015; Resnick et al., 2007) consisted of the forensic rape examination accompanied by a rape crisis counsellor, who provided information about the examination and services available in the community. The standard care in the study of Nixon et al. (2016) combined methods ranging from psychoeducation, supportive counselling, problem-solving, interpersonal therapy elements of mindfulness, acceptance and value-based techniques to discussion of thoughts and feelings. Notably, over the course of the study, participants in the standard care group received more sessions than those receiving cognitive processing therapy. Rothbaum et al. (2012) provided few details about the standard care. However, their control group seemed to receive only medical emergency care, which might be comparable to the standard care of Resnick et al. (2007) and Miller et al. (2015). The two pilot EMDR studies (Tarquinio, Brennstuhl, Reichenbach, Rydberg, & Tarquinio, 2012a; Tarquinio, Schmitt, Tarquinio, Rydberg, & Spitz, 2012b) did not contain a control group and Echeburúa, de Corral, Sarasua, and Zubizarreta (1996) compared two interventions.

Outcome measure

Two studies (Echeburúa et al., 1996; Nixon et al., 2016) reported on the categorical outcome measure of a PTSD diagnosis. PTSD symptom severity was a primary outcome measure of all studies. Miller et al. (2015), Resnick et al. (2007) and Rothbaum et al. (2012) used the PTSD Symptom Scale (PSS) for the DSM-IV and Echeburúa et al. (1996) used the PSS for the DSM-III-Revised (DSM-III-R). Two studies (Tarquinio et al., 2012a, 2012b) used the Impact of Events Scale (IES; Horowitz, Wilner, & Alvarez, 1979), which is a self-report measure of post-trauma intrusions and avoidance symptoms. The hyperarousal dimension of PTSD is not tested in the IES. Lastly, Nixon et al. (2016) used the Clinician-Administered PTSD Scale (CAPS), which is a structured clinical interview assessing PTSD symptoms according to DSM-IV criteria.

Risk of bias of included studies

The risk of bias as assessed by the Cochrane Tool of Bias is summarized for each study in Figure 2. Appendix B contains the judgement of the risk of bias of the individual studies. While all five studies comparing different treatment groups claimed to be randomized trials, true randomization only occurred in two of them (Miller et al., 2015; Rothbaum et al., 2012), meaning that the other studies risk selection bias due to quasi-randomization (Higgins & Green, 2011). Furthermore, although blinding participants and personnel in psychological interventions is impossible, it is possible to blind the outcome assessment. Of the five studies comparing two interventions, only Echeburúa et al. (1996) failed to blind the outcome assessment by having one therapist performing both the therapy and the outcome assessment. Two studies might have been exposed to attrition bias as they reported an as-treated analysis while having significant drop-outs (50–64% in Miller et al. (2015) and 38% in Resnick et al. (2007)). The study of Miller et al. (2015) was the only one that was selective in reporting outcome data. They carried out many analyses between different subgroups of their participants, but only reported exact data of significant differences. Other comparisons were only mentioned in passing: ‘No other statistically significant results were found’ (p.133).
Figure 2.

Risk of bias summary of included studies. The minus sign represents a high risk of bias, the plus sign a low risk of bias, and the question mark an unclear risk of bias. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Risk of bias summary of included studies. The minus sign represents a high risk of bias, the plus sign a low risk of bias, and the question mark an unclear risk of bias. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Reporting of safety and harms

None of the studies reported a strategy for collecting or analysing harms-related information. Accordingly, five studies did not report any data on (serious) adverse events (i.e. fatal or life-threatening events, events that require hospitalization or cause invalidity or disability). Rothbaum et al. (2012) and Nixon et al. (2016) appeared to have adopted a passive strategy of the surveillance of harms, as their results sections stated that there were no (serious) adverse events reported. In addition, most studies did not report drop-outs or the reasons for attrition. Nixon et al. (2016) reported that one participant stopped treatment due to life-threatening illness. Additionally, they reported that two participants who received the intervention showed an increase in clinician-reported PTSD symptom severity at some point during the trial, with one participant reporting higher PTSD symptom severity at the 12-month follow-up than at pretreatment. Due to this lack of safety data, we contacted the authors of the studies for further information and received additional information from Echeburúa et al. (1996), Tarquinio et al. (2012a), Tarquinio et al. (2012b), and Resnick et al. (2007). Echeburúa et al. (1996), Tarquinio et al. (2012a), and Tarquinio et al. (2012b) stated not to have applied a predetermined strategy for the surveillance of harms. Resnick et al. (2007) systematically asked victims about their opinion of the helpfulness of the procedures and no participants had found the trial problematic. Furthermore, Echeburúa et al. (1996), Tarquinio et al. (2012a), Tarquinio et al. (2012b), and Resnick et al. (2007) reported that no (serious) adverse events had occurred.

Prevention of PTSD diagnosis

As previously mentioned, two studies reported the efficacy of the interventions on the development of PTSD after sexual assault based upon the presence of a PTSD diagnosis (Echeburúa et al., 1996; Nixon et al., 2016). When focusing on the difference between groups, Echeburúa et al. (1996) found no difference at any time point in PTSD diagnoses between the group that received cognitive restructuring training and the group that received progressive muscular relaxation training. Similarly, Nixon et al. (2016) found no difference between cognitive processing therapy and standard care in PTSD diagnoses at posttreatment and follow-up.

Reduction of PTSD symptom severity

The results of the within-group and between-group analyses of all studies on PTSD symptom severity are summarized in Table 2.
Table 2.

Effects of interventions of included studies.

CitationFollow-upOutcome measureWithin-group analysis in intervention groupBetween-group analysis
Echeburúa et al. (1996)Posttreatment1, 3, 6, 12 mthPSS-ISignificant decrease in PTSD scores in both cognitive restructuring and progressive muscular relaxation groups.Significantly lower PTSD scores in the cognitive restructuring group than in the progressive muscular relaxation group.
Resnick et al. (2007)6 wks6 mthPSS-SRNo baseline data collected.No significant difference in PTSD scores between the video intervention and standard care.
Rothbaum et al. (2012)4, 12 wksPSS-INo baseline data reported for rape victims separately.Significantly lower PTSD scores in the modified prolonged exposure session compared to assessment only.
Tarquinio et al. (2012a)Pretreatment Posttreatment4 wks, 6 mthIESSignificant decrease in PTSD scores in EMDR participants.Only one intervention, thus no between-group analysis.
Tarquinio et al. (2012b)PretreatmentPosttreatmentIESSignificant decrease in PTSD scores in EMDR participants.Only one intervention, thus no between-group analysis.
Miller et al. (2015)Pretreatment2 wks, 2 mthPSS-SRSignificant increase in PTSD scores at 2-wks follow-up, but not at 2-mth follow-up.aNo significant difference in PTSD scores between the video intervention and standard care.
Nixon et al. (2016)Pretreatment1 wk3, 6, 12 mthCAPSSignificant decrease in PTSD scores in the cognitive processing.Between-group differences remained stable across treatment, indicating that there was no difference between cognitive processing therapy and standard care.

mth = month(s), PSS-I = PTSD Symptom Scale Interview, PTSD = Posttraumatic Stress Disorder, wks = weeks, PSS-SR = PTSD Symptom Scale Self-Report, NR = not reported, IES = Impact of Events Scale, EMDR = Eye Movement Desensitization and Reprocessing, wk = week, CAPS = Clinician-Administered PTSD Scale. aWithin-group analysis calculated from reported means and standard deviations at pretreatment and follow-up assessments.

Effects of interventions of included studies. mth = month(s), PSS-I = PTSD Symptom Scale Interview, PTSD = Posttraumatic Stress Disorder, wks = weeks, PSS-SR = PTSD Symptom Scale Self-Report, NR = not reported, IES = Impact of Events Scale, EMDR = Eye Movement Desensitization and Reprocessing, wk = week, CAPS = Clinician-Administered PTSD Scale. aWithin-group analysis calculated from reported means and standard deviations at pretreatment and follow-up assessments.

Within-group analyses of intervention

All four studies (Echeburúa et al., 1996; Nixon et al., 2016; Tarquinio et al., 2012a, 2012b) that conducted a within-group analysis reported a significant decrease in PTSD symptom severity across the treatment up until the latest follow-up, the longest of which was 12 months. However, without comparing these results to a control group, this decrease in symptoms cannot be differentiated from natural recovery. The remaining three studies did not report a within-group analysis. For Miller et al. (2015) a within-group hedge’s g was calculated using the reported means and standard deviations of the PSS total symptom scores. This revealed a significant increase in PTSD symptom severity from pretreatment to posttreatment (g = 0.90, 95% CI = 0.38, 1.41) that was no longer significant from pretreatment to the 2-month follow-up (g = 0.47, 95% CI = −0.03, 0.97). Rothbaum et al. (2012) and Resnick et al. (2007) did not collect baseline data, therefore calculating within-group analyses was not possible.

Between-group analyses comparing intervention to standard care

Four studies (Miller et al., 2015; Nixon et al., 2016; Resnick et al., 2007; Rothbaum et al., 2012) provided a between-group analysis comparing an intervention to standard care. A meta-analysis of the aggregated data of these four studies did not show a significant effect of early intervention on PTSD symptom severity at the first post-intervention follow-up, as shown in Figure 3. However, at the latest follow-up, early intervention corresponded to significantly lower PTSD severity scores, see Figure 4. No evidence was found for an effect at the first follow-up, ranging from one to 6-weeks post-intervention (random effects) (k = 4, n = 292, g = −0.28, 95% CI = −0.57, 0.02). However, a trend in favour of early intervention can be found in all four studies. There was a moderate level of statistical heterogeneity (I2 = 33%). At the last follow-up, ranging from two to 12-months post-intervention, a modest effect of the early intervention on PTSD symptom severity just reached significance (random effects) (k = 4, n = 293, g = −0.23, 95% CI = −0.46, 0.00). There was no statistical heterogeneity (I2 = 0%).
Figure 3.

Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at first follow-up. The first follow-up post-intervention was: for Resnick et al. (2007) six weeks, for Rothbaum et al. (2012) 4 weeks, for Miller et al. (2015) 2 weeks and for Nixon et al. (2016) 1 week. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Figure 4.

Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at latest follow-up. The latest follow-up was: for Resnick et al. (2007) 6-months post-intervention, for Rothbaum et al. (2012) 12 weeks, for Miller et al. (2015) 2 months and for Nixon et al. (2016) 1 year. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at first follow-up. The first follow-up post-intervention was: for Resnick et al. (2007) six weeks, for Rothbaum et al. (2012) 4 weeks, for Miller et al. (2015) 2 weeks and for Nixon et al. (2016) 1 week. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014. Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at latest follow-up. The latest follow-up was: for Resnick et al. (2007) 6-months post-intervention, for Rothbaum et al. (2012) 12 weeks, for Miller et al. (2015) 2 months and for Nixon et al. (2016) 1 year. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.

Discussion

The goal of this study was to review the safety and efficacy of early interventions in reducing or preventing PTSD after sexual assault. The systematic review identified seven studies that met the eligibility criteria. The included studies investigated a range of different interventions, including EMDR, prolonged exposure, cognitive restructuring, cognitive processing, and a mainly psycho-educational video intervention. Due to this heterogeneity and the small number of studies, the types of interventions could not be examined separately nor compared. The studies were also diverse in research design and timing. The methodological quality of the included studies was mostly low, resulting in a high risk of selection bias. The results firstly show that there is limited documentation on the safety of early intervention after sexual assault. Most studies did not mention safety at all. The passive surveillance of two studies reported no (serious) adverse events. Nixon et al. (2016) found a significant worsening of PTSD symptoms who received the intervention (i.e., cognitive processing therapy) as indexed by the clinical interview. However, these participants did not self-report a worsening in symptoms. In addition, an increase in PTSD symptom severity was also found in two participants in the control condition which suggests that the most likely explanation for the purported symptom increase is a natural course of symptoms. No serious adverse events were found in any of the trials (excluding Miller et al. (2015) due to lack of information). Thus, we have found no evidence to suggest early interventions after sexual assault are unsafe. However, given the debate about potential harm that can be induced by the application of early interventions for PTSD (e.g. Litz et al., 2006), it is quite noteworthy that none of the studies implemented an active strategy to identify potential harm or the occurrence of adverse events during the trial, even though such an active strategy is likely to uncover adverse events (Stephens, Talbot, & Routledge, 1998). In light of the negative effects of psychological debriefing (Rose et al., 2002), a focus on safety should be prioritized in early intervention research. In terms of the prevention of PTSD, early interventions resulted in no fewer PTSD diagnoses than control settings. However, only two studies reported on the differences in post-intervention PTSD diagnosis between groups. The small samples and the heterogeneity of the studies preclude generalization of these findings. With regard to the efficacy of early interventions to reduce PSTD symptom severity, a significant decrease in symptom severity across post-intervention and follow-up was detected in the intervention group of all studies that reported baseline data. Meta-analyses using the data of four studies found no difference at one to 6-weeks post-intervention but revealed that early intervention generated a significantly greater reduction in PTSD symptom severity than standard care at 2–12-months follow-up. In other words, the meta-analyses were unable to find evidence for the efficacy of early intervention on a short term, but did find a trend in favour of early intervention. Additionally, the meta-analysis found evidence for long-term efficacy of the early intervention in reducing the severity of PTSD symptoms. Although this narrow-scoped review of early intervention after sexual assault has not been conducted previously, similar reviews on the broader scope of early post-trauma intervention should be considered. For example, in their review on help-seeking behaviour in sexual assault victims, Dworkin and Schumacher (2016) concluded that early psychological treatment may reduce the risk of posttraumatic stress for the first few months. These findings are in line with the results of the current review. In contrast, a Cochrane review by Roberts et al. (2009) found cognitive behavioural therapy and cognitive restructuring to be the most efficacious in preventing PTSD in trauma patients. Our results do not seem to support this finding in a sample of sexual assault victims, because the two included articles that studied interventions with a cognitive element showed mixed results: More specifically, Echeburúa et al. (1996) reported cognitive restructuring to be more effective than relaxation training at 12 months, whereas Nixon et al. (2016) measured no increased efficacy of cognitive reprocessing over standard care. It should be noted that these studies used different control groups, and the findings of two studies are insufficient to reject the finding of Roberts et al. (2009). Still, the inconsistency in findings underlines the importance of examining interventions after sexual assault in homogenous samples. The studies that were included in this systematic review show noteworthy limitations. Foremost, only seven studies were included in this review, making it difficult to draw reliable conclusions. Additionally, these studies presented methodological and statistical heterogeneity. Particularly, they included a range of interventions, making generalizations on intervention-type unreliable, and had a high risk of bias, which increases the likelihood of a Type I error (Moher et al., 1998). It should also be noted that the included studies presented PTSD symptoms as described by the DSM-III-R or DSM-IV. However, because the current DSM-5 defines PTSD differently by adding the domain of negative cognitions, no generalizations to this definition of PTSD can be made. In light of these limitations, several implications for future research can be drawn. Foremost, as stated before, the safety of early interventions should be taken into consideration in future trials: Future research should report any adverse events, drop-outs or negative effects within the trial sample and should adopt active strategies to detect them. In addition, to determine the efficacy of early intervention in preventing PTSD diagnosis, future efficacy trials should report the prevalence of PTSD diagnosis as well as PTSD symptoms. Furthermore, future research needs to resolve differences in the wide variety of study designs in order to determine the most efficacious type, timing and length of intervention. In doing so, a focus on high quality of design is crucial to reduce the risk of bias. Lastly, future research should compare the effect of early interventions to the effect of standard treatment at a later point in time. Considering the previously stated arguments in favour of early intervention, this type of research should extend beyond the effect on PTSD, and include comorbid psychopathology, cost-effectiveness, and the accessibility for victims of sexual assault. In conclusion, the findings of this review and meta-analyses suggest that early interventions can lead to durable effects on PTSD symptom severity reduction after sexual assault. Therefore, the present study provides support for the development of early interventions. However, due to a limited availability of data, it is not yet possible to draw any definite conclusions about the safety of early interventions after sexual assault, their efficacy and their potential as a preventive treatment for PTSD. Nevertheless, the present review and meta-analysis show that, although psychological debriefing has been found to be ineffective, other interventions can be effective as early intervention after sexual assault. Therefore, we urge researchers not to shy away from this field but instead invest in the exploration and further development of effective interventions to prevent PTSD in victims of sexual assault.
Table B1.

Risk of bias of Echeburúa et al. (1996).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationHigh risk‘in order of arrival’ (p.189)
Allocation concealmentHigh riskSince allocation was based on order of arrival, there cannot have been allocation concealment.
Blinding of participantsHigh riskNo blinding.
Blinding of outcome assessmentHigh riskThe same therapist carried out therapy and assessment.
Incomplete outcome dataLow riskNo drop-outs or treatment changes.
Selective reportingLow riskAll data seem to be reported.
Table B2.

Risk of bias of Resnick et al. (2007).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationHigh riskParticipants presenting on nonprime dates were assigned to the video condition, those on prime dates to the control group.
Allocation concealmentHigh risk‘Project assistants were aware of the designated study condition prior to recruiting participants.’ (p.2435)
Blinding of participantsHigh riskNo blinding.
Blinding of outcome assessmentLow riskThe interviewer was blind to treatment condition throughout the course of the study.’ (p.2438)
Incomplete outcome dataHigh riskAs treated analysis, while 15 participants chose not to watch the video and 5 participants watched less than half after randomization.
Selective reportingLow riskAll data seem to be reported.
Table B3.

Risk of bias of Rothbaum et al. (2012).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationLow riskComputer-generated patient random assignments.
Allocation concealmentLow riskEnvelopes containing … assignments were given to the patient and their nurse … to ensure that assessors remained blind’. (p.958)
Blinding of participantsHigh riskNo blinding.
Blinding of outcome assessmentLow risk‘Blinded assessors administered’ (p.958)
Incomplete outcome dataLow risk‘Missing values for week 4 and week 12 were handled with multiple imputation’ (p.959)
Selective reportingLow riskAll data seem to be reported.
Table B4.

Risk of bias of Tarquinio et al. (2012a).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationN/A 
Allocation concealmentN/A 
Blinding of participantsN/A 
Blinding of outcome assessmentN/A 
Incomplete outcome dataUncertain riskNo data on participant selection and/or drop-outs.
Selective reportingLow riskAll data seem to be reported.
Table B5.

Risk of bias of Tarquinio et al. (2012b).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationN/A 
Allocation concealmentN/A 
Blinding of participantsN/A 
Blinding of outcome assessmentN/A 
Incomplete outcome dataUncertain riskNo data on participant selection and/or drop-outs.
Selective reportingLow riskAll data seem to be reported.
Table B6.

Risk of bias of Miller et al. (2015).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationUncertain riskRandomization procedure not explained.
Allocation concealmentUncertain riskAllocation concealment not reported.
Blinding of participantsHigh riskNo blinding.
Blinding of outcome assessmentLow risk‘trained research assistants, blind to the study condition’ (p.132)
Incomplete outcome dataHigh riskAs treated analysis with 50–64% drop-out rates.
Selective reportingHigh riskResults are only reported according to previous assault status.
Table B7.

Risk of bias of Nixon et al. (2016).

Bias itemAuthors’ judgementSupport for judgement
Random sequence generationHigh risksequentially randomized (1:1 ratio)’ (p.238)
Allocation concealmentHigh riskSince allocation was sequential there cannot have been allocation concealment.
Blinding of participantsHigh riskNo blinding
Blinding of outcome assessmentLow risk‘Assessor … were unaware … of treatment condition’ (p.238)
Incomplete outcome dataLow riskMany missing data, but imputed using appropriate methods.
Selective reportingLow riskAll data seem to be reported.
  27 in total

1.  Prevention of post-rape psychopathology: preliminary findings of a controlled acute rape treatment study.

Authors:  H Resnick; R Acierno; M Holmes; D G Kilpatrick; N Jager
Journal:  J Anxiety Disord       Date:  1999 Jul-Aug

2.  Description of an early intervention to prevent substance abuse and psychopathology in recent rape victims.

Authors:  Heidi Resnick; Ron Acierno; Dean G Kilpatrick; Melissa Holmes
Journal:  Behav Modif       Date:  2005-01

3.  Psychological Outcomes After a Sexual Assault Video Intervention: A Randomized Trial.

Authors:  Katherine E Miller; Christopher C Cranston; Joanne L Davis; Elana Newman; Heidi Resnick
Journal:  J Forensic Nurs       Date:  2015 Jul-Sep       Impact factor: 1.175

4.  Trajectories of PTSD symptoms following sexual assault: is resilience the modal outcome?

Authors:  Maria M Steenkamp; Benjamin D Dickstein; Kristalyn Salters-Pedneault; Stefan G Hofmann; Brett T Litz
Journal:  J Trauma Stress       Date:  2012-07-13

Review 5.  Rape treatment outcome research: empirical findings and state of the literature.

Authors:  Katrina A Vickerman; Gayla Margolin
Journal:  Clin Psychol Rev       Date:  2009-04-17

6.  The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration.

Authors:  Alessandro Liberati; Douglas G Altman; Jennifer Tetzlaff; Cynthia Mulrow; Peter C Gøtzsche; John P A Ioannidis; Mike Clarke; P J Devereaux; Jos Kleijnen; David Moher
Journal:  PLoS Med       Date:  2009-07-21       Impact factor: 11.069

7.  Patterns of lifetime PTSD comorbidity: a latent class analysis.

Authors:  Isaac R Galatzer-Levy; Angela Nickerson; Brett T Litz; Charles R Marmar
Journal:  Depress Anxiety       Date:  2012-12-28       Impact factor: 6.505

8.  Randomized controlled evaluation of an early intervention to prevent post-rape psychopathology.

Authors:  Heidi Resnick; Ron Acierno; Angela E Waldrop; Lynda King; Daniel King; Carla Danielson; Kenneth J Ruggiero; Dean Kilpatrick
Journal:  Behav Res Ther       Date:  2007-05-13

9.  Posttraumatic stress disorder in the National Comorbidity Survey.

Authors:  R C Kessler; A Sonnega; E Bromet; M Hughes; C B Nelson
Journal:  Arch Gen Psychiatry       Date:  1995-12

10.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.

Authors:  David Moher; Alessandro Liberati; Jennifer Tetzlaff; Douglas G Altman
Journal:  PLoS Med       Date:  2009-07-21       Impact factor: 11.069

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  9 in total

1.  Course, Moderators, and Predictors of Acute Coronary Syndrome-Induced Post-traumatic Stress: A Secondary Analysis From the Myocardial Infarction-Stress Prevention Intervention Randomized Controlled Trial.

Authors:  Roland von Känel; Rebecca E Meister-Langraf; Jürgen Barth; Ulrich Schnyder; Aju P Pazhenkottil; Katharina Ledermann; Jean-Paul Schmid; Hansjörg Znoj; Claudia Herbert; Mary Princip
Journal:  Front Psychiatry       Date:  2021-05-14       Impact factor: 4.157

2.  Early intervention with eye movement desensitization and reprocessing (EMDR) therapy to reduce the severity of post-traumatic stress symptoms in recent rape victims: a randomized controlled trial.

Authors:  Milou L V Covers; Ad de Jongh; Rafaële J C Huntjens; Carlijn de Roos; Marcel van den Hout; Iva A E Bicanic
Journal:  Eur J Psychotraumatol       Date:  2021-09-09

3.  Pre-hospital, in-hospital and post-hospital factors associated with sleep quality among COVID-19 survivors 6 months after hospital discharge: cross-sectional survey in five cities in China.

Authors:  Leiwen Fu; Yuan Fang; Dan Luo; Bingyi Wang; Xin Xiao; Yuqing Hu; Niu Ju; Weiran Zheng; Hui Xu; Xue Yang; Paul Shing Fong Chan; Zhijie Xu; Ping Chen; Jiaoling He; Hongqiong Zhu; Huiwen Tang; Dixi Huang; Zhongsi Hong; Xiaojun Ma; Yanrong Hao; Lianying Cai; Jianrong Yang; Shupei Ye; Jianhui Yuan; Yaoqing Chen; Fei Xiao; Zixin Wang; Huachun Zou
Journal:  BJPsych Open       Date:  2021-10-11

4.  Risk factors for PTSD diagnosis in young victims of recent sexual assault.

Authors:  Mirjam L Pijpers; Milou L V Covers; Saskia Houterman; Iva A E Bicanic
Journal:  Eur J Psychotraumatol       Date:  2022-04-05

5.  Serum adiponectin-levels are predictive of probable posttraumatic stress disorder in women.

Authors:  Eileen Vuong; Shibe Mhlongo; Esnat Chirwa; Carl Lombard; Nasheeta Peer; Sian Megan Hemmings; Naeemah Abrahams; Soraya Seedat
Journal:  Neurobiol Stress       Date:  2022-08-08

6.  Examining Associations Between Participant Gender, Desired Partner Gender, and Views Toward Sexually Coercive Behaviors.

Authors:  Danielle J DelPriore
Journal:  Evol Psychol Sci       Date:  2022-09-13

7.  Development of multidisciplinary sexual assault centres in the Netherlands.

Authors:  Milou L V Covers; Wouter Karst; Iva A E Bicanic
Journal:  Eur J Psychotraumatol       Date:  2022-09-29

8.  Mobile Insight in Risk, Resilience, and Online Referral (MIRROR): Psychometric Evaluation of an Online Self-Help Test.

Authors:  Manon A Boeschoten; Hans Te Brake; Merel Marjolein van Herpen; Niels van der Aa; Miranda Olff
Journal:  J Med Internet Res       Date:  2020-09-25       Impact factor: 5.428

9.  Sexual function and pelvic floor activity in women: the role of traumatic events and PTSD symptoms.

Authors:  Matty D A Karsten; Vincent Wekker; Anne Bakker; Henk Groen; Miranda Olff; Annemieke Hoek; Ellen T M Laan; Tessa J Roseboom
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  9 in total

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