| Literature DB >> 35370831 |
Carolyn Ponting1,2, Guido G Urizar3, Christine Dunkel Schetter1.
Abstract
Anxiety symptoms are common among pregnant women worldwide. In the United States, prenatal anxiety symptoms tend to be elevated among Black and Latin American women as compared to non-Latina White women. Despite the high prevalence of anxiety and associations with adverse maternal and offspring outcomes, interventions have not been developed or tailored sufficiently to Black women or Latinas who need efficacious treatment. This article provides a scoping review of articles published since 2017 that test the effects of randomized and non-randomized psychological interventions designed to reduce prenatal anxiety in samples comprised primarily of ethnic/racial minority women. We also review published protocols of planned psychological interventions to reduce prenatal anxiety in order to highlight novel approaches. In addition to summarizing intervention efficacy and participant acceptability, we highlight gaps in the literature which, if addressed, could improve perinatal mental health equity. Finally, we discuss future directions in prenatal anxiety intervention science beginning preconception including intervention design and prevention models.Entities:
Keywords: Black/African American Latinx/Latina; anxiety; intervention; prenatal mental health; scoping review
Year: 2022 PMID: 35370831 PMCID: PMC8965279 DOI: 10.3389/fpsyt.2022.820343
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Figure 1PRISMA scoping review flow diagram for study inclusion.
Design, measurement, hypotheses and results of reviewed studies.
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| Lenz and Potts ( | (a) individual (b) IPT (c) 9 sessions (one ethnographic introductory session + 8 IPT sessions); plus maintenance treatment session if participant finish all nine sessions (d) Clinical Psychologists, master's level clinicians (e) research clinic, participant homes, or other community locations | RCT | Women in both the intervention and enhanced prenatal care groups did not show significant reductions in anxiety symptoms (STAI-Brief). | Not reported | Participants assigned to brief-IPT reported high scores on the Client Satisfaction Questionnaire at the 37–39 weeks assessment (IPT |
| Ruiz et al. ( | (a) individual (b) ACT and Problem-Solving Therapy (c) six sessions (d) Nurse practitioners (NPs) or certified nurse midwives (e) primary clinic, OBGYN office | Pilot Pre-Post design | Women in the intervention group showed significant reductions in anxiety symptoms (BAI) between baseline and post-intervention ( | Yes: “considerations for family roles and hierarchies, culturally relevant metaphors/mindfulness exercise” | High satisfaction ratings ( |
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| Atif et al. ( | (a) individual OR group (b) CBT (c) six sessions, time client dependent ~1 h, option for up to six booster sessions (d) Para-professionals (bachelor's level volunteers with no prior mental health training with nursing backgrounds) (e) hospital | RCT | Primary hypothesis: The intervention will address symptoms of anxiety as measured by the HADS before these become chronic, severe, and debilitating, and therefore will be preventative, allowing women to learn strategies for stress management and problem solving before the symptoms become ingrained. | Yes: “The intervention used culturally appropriate illustrations and examples of healthy activities to set tasks in collaboration with women to encourage engaging unhelpful behaviors” | An initial sample of five women rated the intervention as helpful and acceptable to them and their family members; resulting in greater awareness of their feelings, stress management and strategies to improve wellbeing. |
| Bright et al. ( | (a) individual (b) online IPT (c) six 30-min sessions (d) none, self -guided (e) online | RCT | Primary hypothesis: Participants randomized to the intervention will have clinical levels of anxiety at lower percentages post-treatment than women randomized to routine care as measured by the DASS-21. | None stated. | Planned assessment of percentage of participants who report the modules and activities in the intervention as easily understood and navigated to measure acceptability. |
| Challacombe et al. ( | (a) individual (b) CBT (c) Fout to five 2-h sessions vs. 8–10 1-h sessions (d) “experienced therapists” (e) national publicly funded healthcare setting | RCT | Primary hypothesis: Participants with clinical diagnoses of OCD, PTSD, Social Anxiety or Panic Disorder randomized to time intensive or standard weekly intervention will show reductions in anxiety as measured by the GAD-7 or disorder specific measures (e.g., OCI for OCD, MI for Panic Disorder, IES for PTSF, SPIN for Social Anxiety). | None stated. | Planned qualitative interviews to assess acceptability of recruitment methods, assessment measures, intervention mode, and delivery. |
| Jackson et al. ( | (a) individual (b) CBT (c) eight sessions (d) Perinatal clinical nurse specialist (e) hospital-based perinatal outpatient program | RCT | Primary hypothesis: Participants randomized to the intervention will show less anxiety than those in the control condition, as measured by the STAI. We also hypothesize this study will be feasible in terms of fidelity and deliverability, as well as be highly acceptable to participants. | None stated. | Four open-ended qualitative questions planned to assess acceptability. |
| Loughnan et al. ( | (a) individual (b) iCBT (c) three sessions, time client dependent ~1 h (d) None- self-guided (e) client's choice (remote, online) | RCT | Primary hypothesis: Participants randomized to the intervention will show significantly fewer symptoms of anxiety compared to those in usual care, as measured by the GAD-7. | None stated. | – |
| Melnyk et al. ( | (a) group (b) CBT + positive parenting (c) six 2-h sessions (d) advanced practice nurses (e) prenatal clinic | RCT | Primary Hypothesis: Participants randomized to the intervention will show significantly less anxiety at 4–6 weeks postpartum (3months post-intervention), and at 6 moths postpartum (8 months post-intervention) than will participants in the attentional control condition as measured by the GAD-7. | Yes: “sessions that are culturally sensitive, readable at the sixth grade reading level and focused on empowering pregnant minority women to engage in healthy lifestyle behaviors”. Prior delivery with ethnic/racial minority women. | – |
| O'Brien et al. ( | (a) group (b) Enhanced Triple P for Baby (positive parenting program); Mellow Bumps (reflective functioning, self-care, parenting) (c) four 2-h sessions (ETPB); six 2-h sessions (MB) (d) facilitators with health visiting or midwifery backgrounds (e) multiple | RCT | Primary Hypothesis: Women randomized to either intervention will show reduced anxiety as compared to women receiving usual care. | Yes: Planned interviews with the Heads of Midwifery planned delivery settings to gain further insights into the ways in which the local context and organizational culture might have impacted recruitment | Documented acceptability in high deprivation contexts in prior research studies. |
| Zuccolo et al. ( | (a) individual (b) Motherly app (behavioral activation) plus brief online CBT (c) four sessions (d) Psychologists certified in CBT (e) online | RCT | Primary Hypothesis: Participants receiving the Motherly app plus brief online CBT will show significantly greater reduction in symptoms of anxiety (secondary outcome) as compared with participants who receive only psychoeducation in addition to brief online CBT as measured by the GAD-7. | Yes: Treatment targets (e.g., physical activity, nutrition) were specifically selected based on research findings regarding risk factors for individuals from low-income countries. Intervention uses recommendations based on those from Brazilian Ministry of Health. Online delivery of CBT selected due to dearth of human and financial resources in Brazil. | – |
ACT, Acceptance and Commitment Therapy; CBT, Cognitive Behavioral Therapy; iCBT, internet-delivered Cognitive Behavioral Therapy; ETPB, Enhanced Triple P for Baby; IPT, Interpersonal Therapy; MB, Mellow Bumps; RCT, Randomized Control Trail; BAI, Beck Anxiety Inventory; GAD-7, Generalized Anxiety Disorder- 7item; HADS, Hospital Anxiety and Depression Scale; STAI, State-Trait Anxiety Inventory; DASS-21, Depression, Anxiety and Stress Scale-21; OCI, Obsessive Compulsive Inventory-Revised; MI, Mobility Inventory; IES, Impact of Events Scale; SPIN, The Social Phobia Inventory.
Assessment of study bias.
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| Lenze and Potts ( | ⊕ | ⊕ | ⊕ | ∅ | ⊕ | ⊕ | ⊕ | Low |
| Ruiz et al. ( | ⊗ | ⊗ | ⊗ | ⊗ | ∅ | ⊕ | ⊕ | High |
⊕Indicates low risk of bias, ∅indicates unclear risk of bias, and ⊗indicates high risk of bias. Studies rated as “low risk of bias” on four of the six categories were considered to have an overall low risk of bias; studies with two or three categories rated as “low risk of bias” were considered to have an overall medium risk of bias; and studies with one or fewer categories rated as “low risk of bias” were considered to have an overall high risk of bias.