| Literature DB >> 33231846 |
Mobolaji Ibitoye1,2, Hope Lappen3, Robert Freeman4, Ashly E Jordan5,6, Ian David Aronson4,5.
Abstract
HIV testing rates remain low among youth ages 13-24 in the US, with only 55% of HIV-positive youth aware of their serostatus. We conducted a systematic review to assess the utility of technology-based interventions to increase point-of-care youth HIV testing and linkage to care. We searched PubMed, Embase, CINAHL, and Cochrane CENTRAL for randomized controlled trials of technology-based interventions aimed at increasing point-of-care youth HIV testing, published between 2008 and 2020. All identified citations were independently screened for inclusion by two authors, and the Cochrane Risk of Bias Tool for Randomized Controlled Trials was used to assess the quality of included studies. Three studies met all inclusion criteria. Two interventions were effective in increasing HIV testing, while one was effective at linkage to care. Technology-based interventions have the potential to increase youth HIV testing in clinical settings and facilitate linkage to care, possibly reducing undiagnosed HIV among adolescents and emerging adults.Entities:
Keywords: Clinical settings; HIV testing; Point-of-care testing; Technology-based interventions; Youth
Mesh:
Year: 2020 PMID: 33231846 PMCID: PMC7684145 DOI: 10.1007/s10461-020-03112-9
Source DB: PubMed Journal: AIDS Behav ISSN: 1090-7165
Initial PubMed search strategy (2008–2018)
| 1 | ("Young Adult"[mesh] OR “Adolescent”[mesh] OR adolescent[tiab] OR adolescents[tiab] OR “young adult”[tiab] OR “young adults”[tiab] OR teen[tw] OR teens[tiab] OR teenage[tiab] OR teenager[tiab] OR teenagers[tiab]) |
| 2 | ("AIDS Serodiagnosis"[mesh] OR "HIV Antibodies/analysis"[mesh] OR "HIV Antigens/analysis"[mesh] OR “HIV Infections/diagnosis”[mesh] OR “HIV Seropositivity/diagnosis”[mesh] OR "HIV Infections/prevention and control"[mesh] OR hiv test*[tiab]) |
| 3 | (“HIV"[mesh] OR “HIV Infections”[mesh] OR "Acquired Immunodeficiency Syndrome"[mesh] OR hiv[tw]) |
| 4 | (“Mass Screening”[mesh] OR "Serologic Tests"[mesh] OR "Diagnosis"[mesh] OR "diagnosis" [Subheading] OR "prevention and control" [Subheading] OR screening[tiab] OR test[tiab] OR tests[tiab] OR tested[tiab] OR testing[tiab]) |
| 5 | #3 and #4 |
| 6 | #2 or #5 |
| 7 | ("Ambulatory Care Facilities"[mesh] OR "Emergency Medical Services"[mesh:noexp] OR "Emergency Services, Psychiatric"[mesh] OR "Emergency Service, Hospital"[mesh] OR "Point-of-Care Systems"[mesh] OR "Ambulatory Care"[mesh] OR "Primary Health Care"[mesh] OR emergency department*[tiab] OR “emergency care”[tiab] OR “urgent care”[tiab] OR “point of care”[tiab] OR “general practice”[tiab] OR “primary care”[tiab] OR outpatient[tiab] OR clinic[tiab] OR clinics[tiab] OR clinical[tiab] OR "Hospitalization"[mesh] OR "Critical Care"[mesh] OR inpatient[tiab] OR "Community Health Services"[mesh] OR ambulatory[tiab] OR community setting*[tiab]) |
| 8 | (“Computer systems”[mesh] OR “Educational Technology”[mesh] OR “Text Messaging”[mesh] OR “Cell Phone”[mesh] OR “software”[mesh:noexp] OR “telemedicine”[mesh] OR “online systems”[mesh:noexp] OR “reminder systems”[mesh] OR “information systems”[mesh:noexp] OR “user-computer interface”[mesh] OR “mobile applications”[mesh] OR “video games”[mesh] OR “videotape recording”[mesh] OR “videodisc recording”[mesh] OR “computer-assisted instruction”[mesh] OR technology[tiab] OR technologies[tiab] OR computer*[tiab] OR smartphone*[tiab] OR ehealth[tiab] OR mhealth[tiab] OR telehealth[tiab] OR texting[tiab] OR text messag*[tiab] OR sms[tiab] OR cell phone*[tiab] OR mobile phone*[tiab] OR cellular phone*[tiab] OR mobile device*[tiab] OR ipad*[tiab] OR tablet[tiab] OR tablets[tiab] OR “mobile app”[tiab] OR "mobile apps"[tiab] OR mobile application*[tiab] OR “web based”[tiab] OR “network based”[tiab] OR audiovisual[tiab] OR multimedia[tiab] OR video[tiab] OR videos[tiab] OR videorecord*[tiab]) |
| 9 | ("2008/01/01"[PDAT]: "2018/12/31"[PDAT]) |
| 10 | #1 and #6 and #7 and #8 and #9 |
Fig. 1PRISMA flowchart of study selection
Summary and characteristics of studies included in the systematic review
| Calderon et al. 2011 [ | Merchant et al. 2011 [ | Kurth et al. 2013 [ | |
|---|---|---|---|
| Study characteristics | |||
| Setting | Emergency department in urban area (New York City), July 2008–November 2008 | Emergency department in urban area (New England), October 2007–September 2008 | Emergency department in urban area (Pacific Northwest), during a period when the ED only provided HIV testing if clinically indicated or in the event of occupational blood exposure |
| Sample size | 200 | 571 | 517 |
| Age range | 15–21 years | 18–64 years (25% of participants < 22 years) | 18 years and older (Inta: 3% < 20, 31% 20–29) Ctrlb: 6% < 20, 26% 20–29) |
| Sex | Female: 47.5% Male: 52.5% | Female: 62.2% Male: 37.8% | Female: 41% (Int); 38% (Ctrl) Male: 59% (Int); 62% (Ctrl) |
| Intervention | A 4-minute pre-test HIV educational video covering the seven essential elements required by New York State law for HIV pretest counseling which included information on HIV transmission, HIV infection and AIDS, the HIV test, benefits of testing, voluntary and mandatory testing, results reporting requirements and partner notification | An audio, computer-assisted, interview system-based HIV risk questionnaire (described below) plus tailored feedback messages to participants’ reported HIV risk behaviors. Feedback messages were provided immediately after each question and were directed to the participant (i.e. “you”) both verbally (via audio recording) and written on the computer screen. The feedback messages did not mention HIV testing | The Computer Assessment and Risk-reduction Education (CARE) tool is a theory-based (Integrative Model of Change and Social Cognitive Theory) intervention which includes a risk assessment, a rapid HIV test video, HIV test consent, personalized feedback on reported risks, tailored behavioral skill-building videos, and development of a specific HIV risk-reduction plan which was printed out at the end of the session. Chart review was also conducted after the visit similar to the control group |
| Control condition | An in-person HIV counseling session of unspecified duration from a counselor trained to provide age-appropriate, culturally-sensitive HIV education and counseling | An audio, computer-assisted, interview system-based HIV risk questionnaire which asked participants about their self-perceived HIV risk twice–before and after they reported their sexual and injection drug use-related HIV risk behaviors. Participants completed the questionnaire on a tablet personal computer with headphones | Standard care–an emergency department visit and chart review to assess risk behaviors and HIV/STI test referrals |
| Results | |||
| Willingness to test and HIV testing uptake | Intervention group participants were more willing to be tested for HIV [51% (Int) vs. 22% (Ctrl); p < 0.01] and more likely to get an HIV test [aOR:3.6; 95% CI 1.8–7.2; p < 0.001] | Overall, HIV testing uptake was greater in the control group than in the intervention group [55.5% (Ctrl) vs. 54.1% (Int); Δ = − 0.01%; 95% CI 0.09% to 0.07%)] More women in the intervention group were willing to be tested regardless of the effect of the intervention on their self-perceived HIV risk (80% vs. 52.8% with decreased risk perception; 51% vs 33% with no change in risk perception; 73% vs 68% with increased risk perception). Among men, those in the control group were more willing to test (36% vs 89% decreased; 50% vs 54% no change; 59% vs 80% increased) | 97% of intervention group participants were HIV tested, one participant who was not tested as part of the study was tested by ED clinicians. No one in the control group was HIV tested, but two participants were referred elsewhere for an HIV test |
| HIV diagnosis and linkage to care | No one tested HIV positive | There was one true positive and two false positive HIV test results (0.4% seroprevalence; 95% CI 0.01–2.2). The HIV positive person was linked to care in the hospital-based HIV clinic | |
| Acceptability of intervention and satisfaction with testing experience | Intervention group participants reported more satisfaction with the testing experience [Mean satisfaction score: 28.6 out of 30 (Int) vs. 25.4 (Ctrl); p < 0.0001] | Acceptability of the intervention was high in terms of ease of use (97%), privacy (96%), helpfulness compared to face-to-face counseling (91%), and duration (86%); 55% would choose computer-based HIV counseling in the future. In verbal exit interviews, participants reported that the CARE tool was more private (83%), convenient (77%), more comfortable (76%), safer (72%), and more helpful (54%) compared to staff-delivered counseling Intervention group was more likely to be “very satisfied” with their visit (54% vs. 46%) | |
| Post-intervention HIV knowledge or risk perception | Intervention group participants reported higher HIV knowledge scores [78.5% (Int) vs. 66.3% (Ctrl); p < 0.0] | The intervention and control groups did not significantly differ on change in self-perceived HIV risk | Two-thirds of participants in the intervention group thought it was “very important” to change their behaviors to reduce their risk for HIV infection |
| Unmet need potentially addressed by intervention | More HIV risk was identified through the intervention than in the control condition (risk from sexual contact 59% vs 1%; injection drug use 26% vs 2%) and more HIV risk reduction plans were made (98% vs 1%). Most (84%) of participants who made risk reduction plans felt very confident about their ability to change their behaviors | ||
aInt intervention
bCtrl control
Risk of bias of included studies