HIV/AIDS Clinical Trial
— Project YES!Official title:
Transitioning Adolescents to HIV Self-Management in Zambia (Known as: Project YES: Youth Engaging for Success)
Verified date | October 2019 |
Source | Johns Hopkins Bloomberg School of Public Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Youth-led strategies remain untested in clinic-based programs to achieve viral suppression (VS) and reduce self-stigma (feelings of worthlessness/shame) among adolescents and young adults (AYA) living with HIV in sub-Saharan Africa. In response, Project YES! will conduct a randomized controlled trial to test the impact of a theory-based intervention that places trained and paid HIV-positive youth peer mentors (YPMs) in four HIV clinics in Ndola, Zambia. AYA, ages 15 to 24 years, will be randomly assigned to either an intervention arm, consisting of monthly one-on-one and small group sessions with a YPM and optional caregiver support groups, or a usual care arm. Survey data and blood samples will be collected and analyzed to test the hypothesis that youth who are in the intervention group will experience more viral suppression than youth in the comparison group.
Status | Completed |
Enrollment | 276 |
Est. completion date | June 20, 2019 |
Est. primary completion date | February 19, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years to 24 Years |
Eligibility |
Inclusion Criteria: - In the age range of 15-24 years - Aware of her/his HIV status - On cART for at least six months - Speaks Bemba or English - Not planning to move out of the district in the next 18 months - Planning to be available to attend study activities over the next 18-months, as needed Exclusion Criteria: - Being too sick to participate - Attending boarding school - Having a sibling already enrolled in the study (one youth per household) - Having participated in the recent NIH-funded R34 Positive Connections intervention |
Country | Name | City | State |
---|---|---|---|
Zambia | Arthur Davison Children's Hospital | Ndola | Copperbelt Province |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins Bloomberg School of Public Health | Arthur Davison Childrens Hospital, Population Council, United States Agency for International Development (USAID) |
Zambia,
Amzel A, Toska E, Lovich R, Widyono M, Patel T, Foti C, Dziuban EJ, Phelps BR, Sugandhi N, Mark D, Altschuler J; Child Survival Working Group of the Interagency Task Team on the Prevention and Treatment of HIV-infection in Pregnant Women, Mothers and Children. Promoting a combination approach to paediatric HIV psychosocial support. AIDS. 2013 Nov;27 Suppl 2:S147-57. doi: 10.1097/QAD.0000000000000098. Review. — View Citation
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of Participants with Viral Suppression (<1000 copies/mL) at Baseline and Midline | <1000 copies/mL | ~ 6 months (from baseline to midline) | |
Secondary | Proportion of Participants with Internalized Stigma (binary, yes to two out of three questions) at baseline and midline. | Internalized stigma was measured at both time points using three agree/disagree questions from the Internalized AIDS Stigma Scale (IA-RSS) (Kalichman et al. AIDSCare 2009). This measure asks participants to either "agree" or "disagree" with each of the following three statements: (1) You feel guilty that you are HIV positive; (2) You are ashamed that you are HIV positive; and (3) You sometimes feel worthless because you are HIV positive to measure self-stigma (also known as internalized stigma). Responses range from 0-3 with 3 indicating higher/worse experiences of internalized stigma. From this data, a binary outcome was generated with "1" indicating that the participant answered "agree" to at least two of the three questions, and "0" otherwise. | ~ 6 months (from baseline to midline) | |
Secondary | Proportion of Participants with Antiretroviral Adherence Treatment Gap at baseline and midline | >= 48 consecutive hours or more of missed ART (self-reported) | ~ 6 months (from baseline to midline) |
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