HIV - Human Immunodeficiency VirusNCT07221201
Integrating Project YES! With WHO-Endorsed Mental Health Approaches Among Youth Living With HIV
A study testing Project YES+ intervention arm in people with HIV - Human Immunodeficiency Virus and Mental Health, run by Johns Hopkins Bloomberg School of Public Health at 1 site in Zambia.
Trial summary
The proposed study will address the intersecting stigmas of HIV, violence and depression among adolescents and young adults (15-24) living with HIV (AYALHIV) in Zambia. The study will integrate a WHO-endorsed mental health approach into an existing HIV-stigma-reducing intervention, and refine measures of internalized… Read more about this study
- Who is it for?
- Ages 15 years and older
- Conditions the study is for
- HIV - Human Immunodeficiency Virus, Mental Health, Anxiety
- What is being tested?
- Project YES+ intervention arm
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 323 participants
- Where
- 1 siteZambia
- Study dates
- 25 Oct 2025to 30 Jun 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 15 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- For youth
- Be between ages 15-21
- living within 30-minutes, by personal transportation, of the clinic by self-report,
- and being available to attend sessions and data collection over a 4-8 month time period On ART for at least 6 months
- On first-line ART
- Speaks Bemba
Show all 12Show fewer
- For caregivers
- Being 25 years of age or older
- Caring for an AYALHIV who meets the study eligibility criteria
- Speaks Bemba
- Living within 30-minutes, by personal transportation, of the clinic by self-report
- Being available to attend sessions and data collection over a 4-8 month time period
Who cannot join
- For youth,
- only one youth per household may join.
- Also participants will be excluded from joining the RCT if they are at imminent risk of suicide based on WHO guidance on the Self Help plus program.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Reducing the Intersecting Stigmas of HIV, Violence Victimization, and Mental Health: a Randomized Controlled Pilot Integrating Project YES! Youth Engaging for Success With WHO-Endorsed Mental Health Approaches Among Youth Living With HIV in Ndola, Zambia
The proposed study will address the intersecting stigmas of HIV, violence and depression among adolescents and young adults (15-24) living with HIV (AYALHIV) in Zambia. The study will integrate a WHO-endorsed mental health approach into an existing HIV-stigma-reducing intervention, and refine measures of internalized and intersecting stigmas, to create and test the feasibility of Project YES+- a combined youth peer mentoring and lay mental health intervention. This research aims to shift HIV care and treatment for AYALHIV by addressing the multiple internalized and intersecting stigmas that impeded antiretroviral adherence and HIV viral suppression.
Read the detailed description
Nine out of ten AIDS-related deaths among adolescents occur in sub-Saharan Africa (SSA). Despite advances in antiretroviral combination therapy (ART), AIDS-related mortality among adolescents has only decreased 33% since 2010, compared to 66% among children. This slow decline in adolescent deaths is attributed in part to incomplete adherence to ART and subsequent viral failure. Only an estimated 34% of AYALHIV in Zambia, ages 15-24 years, have achieved viral suppression (<1000 copies/mL).
Stigma is increasingly recognized as a modifiable factor impacting ART adherence and viral suppression. Stigma as defined by Goffman is the social devaluation of a person due to an attribute discredited by society, with Parker and Aggleton critically examining stigma as a tool that reinforces inequalities. Different frameworks, such as the mental illness stigma framework and the HIV stigma framework, further delineate stigma into mechanisms experienced by people without the attribute, with the mechanisms being stereotypes, discrimination, and prejudice leading to social rejection, and those with the attribute, with the mechanisms being enacted (experienced), anticipated (beliefs about how others will treat you) and internalized stigma (accepting negative views and devaluing one's self) impacting physical, mental and social health. In this proposed research the investigators focus on internalized HIV stigma among AYALHIV, as well as internalized stigma related to the prevalent youth experiences of violence and depression. Further, the investigators also focus on intersectional stigma, capturing anticipated stigma associated with the complex reality of AYALHIV's multiple social identities instead of one specific attribute. This focus responds directly to this RFA and priority NIH/NIMH future directions for stigma-related research. Evidence shows that internalized stigma is related to viral failure and ART adherence among adults in SSA. Systematic review articles have also examined HIV-internalized stigma interventions; however, a 2019 systematic review of HIV self-stigma interventions in low- and middle-income countries found only one youth focused study from Thailand. In a more recent narrative review, two articles were AYALHIV specific, with only one measuring internalized stigma. In response to this distinct gap in stigma-reducing interventions, and informed by our team's preliminary studies, the investigators developed and tested Project YES! Youth Engaging for Success, to address internalized stigma and HIV outcomes among AYALHIV.
Project YES! is a peer-led facility-based youth mentoring program and is the only CDC evidence-based intervention (EBI) developed in SSA that reduced HIV-internalized stigma among AYALHIV ages 15-24. This RCT found that peer mentoring versus standard of care (SOC) decreased the relative odds of HIV-related internalized stigma (feelings of shame, guilt and worthlessness) by a factor of 0.39 (95% CI:0.21,0.73).) In a stratified analysis, intervention versus SOC participants from a pediatric clinic had a relative increase in the odds of viral suppression (VS) by a factor of 4.7 (95% CI:1.84, 11.78). However, study data also highlighted critical intervention gaps: 74% of AYALHIV experienced physical, sexual and/or emotional violence in the past year, with those experiencing violence at greater risk of viral failure (see preliminary studies).(17) Additionally, AYALHIV who screened positive for depression were less likely to achieve VS (53% vs 62%). Research among South African AYALHIV identified significant, multidirectional pathways linking HIV status and internalized stigma through violence victimization, depression and anticipated stigma, and mental health research clearly links internalized stigma with depression. Few studies, however, examined the relationship between internalized stigma and HIV outcomes, with one finding the impact of discrimination on reduced HIV care retention heightened by internalized stigma. With an estimated 25% of AYALHIV experiencing depression, and the high levels of violence in this population, the investigators must effectively intervene on these pathways to improve HIV outcomes during a developmental stage when youth are "developing and consolidating their sense of self".
To address these gaps the investigators propose integrating WHO-endorsed and lay delivered mental health approaches (e.g. PM+, SH+ and EASE) into our peer mentoring EBI (Project YES!) to create and test Project YES+. The World Health Organization, has various psychological management programs to address mental health conditions through lay workers. Examples of these mental health approaches include Project Management Plus (PM+) and Self Help+, both designed for adults 18+ years, and the Early Adolescent Skills for Emotions (EASE) program designed for young adolescents 10-14 years. While efficacious, the targeted age groups leave a clear gap in service options for 15-19 year olds. By adapting and integrating these mental health approaches into Project YES+, the investigators will specifically provide AYALHIV with problem-management skills through lay peer mentors shown to reduce depression and anxiety. The investigators hypothesize that Project YES+ will also reduce related internalized and intersecting stigmas and improve HIV outcomes. Our refinement of stigma measures will also advance the field's ability to test stigma-reducing interventions to disrupt the pathways among violence, depression, internalized stigma and HIV-related health outcomes. This proposed research will contribute to the field of HIV empirical research and care practices by refining measures and pilot testing a feasible peer led intervention designed to reduce stigma and achieve undetectable viral loads among AYALHIV 15-24 years of age.
STUDY DESIGN The development and pilot testing of Project YES+ will occur in two phases. Phase one has been completed and addressed Aim 1: to integrate an adapted WHO endorsed mental health intervention into Project YES! and Aim 2: to refine stigma measures. To achieve aim 1 the study team first worked with WHO to identify the most promising packages and components to adapt (e.g. PM+, SH+, EASE). After honing in on the key approaches, the investigators then held co-design workshops with AYA and caregivers to refine the Project YES+ To achieve Aim 2, to refine stigma measures, the team conducted cognitive interviewing with youth and caregivers. This phase 1 produced: 1) an age-and-culturally relevant AYALHIV stigma reduction intervention linked to mental health and HIV outcomes, and 2) adapted measures of intersectional, violence-, and depression-related stigmas for AYALHIV.
Phase two is the focus of this registration with clinicaltrials.gov. For phase two, the study team will address Aim 3: to pilot test the intervention, collecting pilot Project YES+ outcomes by conducting an RCT with 50 intervention and 50 comparison AYALHIV and their caregivers who attend HIV care at the Arthur Davison Children's Hospital (ADCH) in Ndola, Zambia (expanding to other clinics if needed to reach the sample size). Individual-level AYA study measures, including stigma, depression, violence, ART adherence, and blood draws for viral testing, will occur at baseline and endline. This data will advance our knowledge on stigma measures and the integration of mental health care in an effective HIV stigma reducing intervention to address the bi-directional associations among HIV, depression, violence victimization, and various internalized stigmas. This data will provide the foundation for a future impact study of Project YES+ on AYALHIV stigmas and HIV outcomes. The specific aim 3 is detailed below:
Aim 3: The purpose of Aim 3 is to test the feasibility of conducting Project YES+ among AYALHIV to prepare preliminary evidence and working knowledge to test the intervention impact in the future. To assess whether 90% of AYAHLIV will attend at least 80% of the intervention sessions with a 90% confidence interval and a margin of error + 10, the investigators will need a minimum sample size of 25 AYALHIV in each study arm. A group sample size of 50 though, will allow us to achieve 74% power to detect a two-sided difference with an alpha of 0.05 of 25 points between the two groups on internalized stigma related to HIV, violence or depression. The investigators know from Project YES! data that a reduction of this size in HIV-internalized stigma is possible. In addition, this sample size will provide valuable data on the proportion of participants reducing psychological distress. At baseline 100% of all AYALHIV participants will have have a positive screen for the Kessler 6 measure of psychological distress and the investigators assume some variability in the proportion with a positive Kessler 6 score in the control group at endline. Group sizes of 50 will achieve 80% power to detect a 20% difference in the Kessler 6 from 95% to 75% between the control and intervention group for a two-sided comparison with alpha=0.05.
- Conditions
- HIV - Human Immunodeficiency Virus, Mental Health, Anxiety, Depression in Adolescence, Stigma
- Being tested
- Project YES+ intervention arm
- Keywords
- HIV, Adolescents, Caregivers, Africa, Youth, Intervention
- Medical subject headings
- Acquired Immunodeficiency Syndrome, Psychological Well-Being, Anxiety Disorders, Social Stigma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Project YES+ intervention armBehavioural
Project YES+ integrates Project YES!
| Study group | Role | What they receive |
|---|---|---|
| Standard of Care | No intervention | The comparison group will receive the standard of care. Standard of care at ADCH includes an optional monthly AYALHIV youth group. The comparison arm participants will also be offered referrals to health care providers if they screen positive for depression or have experienced severe forms of violence (a process the investigators utilized and refined during the Project YES! study). |
| Project YES+ intervention arm | Experimental | Project YES+ will be about 4 months and will consist of an orientation meeting with the youth client, their caregiver, the healthcare worker and the youth peer mentor to introduce the intervention. Youth clients will then meet with their YPM individually and in groups with other youth living with HIV in the intervention, and go through the WHO- Self Help plus group meetings. Caregivers will also attend three different caregiver group meetings. At the end, there will be a transition group meeting with youth and caregivers together, followed by one last individual mentoring meeting with the youth. All individual and group meetings are facilitated by the youth peer mentor. Study team members will provide reminder calls for youth and their caregivers before intervention meetings and data collection points. Receives: Behavioral: Project YES+ intervention arm |
What is being measured
The primary outcome is the main question the study is designed to answer.
Feasibility of intervention as assessed by percentage of sessions attended
Feasibility of 90% of AYAHLIV attending at least 80% of the intervention sessions with a 90% confidence interval and a margin of error + 10.
Measured: Up to 4 months
Number of intervention participants who report they would recommend Project YES+ to their peers
The endline question is "Overall, you would recommend/not recommend this program to another youth living with HIV" with the response options would recommend, would not recomment, decline to answer"
Measured: up to 4 months
Number of intervention participants who would recommend Project YES+ for caregivers
This outcome will be assessed during endline with the question "Overall, you would recommend/not recommend this program to a caregiver of a another youth living with HIV"
Measured: up to four months
Secondary outcomes (1)
Number of youth participants with a positive composite score consisting of psychological distress (Kessler 6) and one positive stigma score (internalized, violence, mental health and intersectional stigma).
The scales for youth are defined as follows: Kessler 6 measures psychological distress with 6 items and a 4 point likert scale (none of the time to all of the time, 0-24 higher score indicates more psychological distress). Internalized stigma is a 3 point self-stigma scale, with yes/no responses (range is 0-3, higher score indicates more self-stigma). Violence is from the adapted IPV stigma scale that has 19 scale items and a 4 point likert response (disagree alot to agree a lot, 0-76 range with a higher score indicating more violence related stigma). An adapted self-stigma of depression scale consists of 15 items and a 4-point likert scale (disagree alot to agree a lot, 0-60 range, with higher scores indicating more depression related stigma). The adapated intersectional anticipated stigma scale from the intersectional discrimination index and has 9 items and a 4-point likert response (disagree alot to agree a lot, 0-36 range, higher scores indicating more stigma).
Measured: Baseline up to approximately 4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Oct 2025
- Study start25 Oct 2025
- Primary completion30 Jun 2026
- Study completion30 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (26)Papers the sponsor has linked to this study.
- Other trials for HIV - Human Immunodeficiency VirusStudies of the same condition, open and under way.
- More trials run by Johns Hopkins Bloomberg School of Public HealthThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomized Controlled Trial (Individual Level)
- Masking
- None (open label)
- Enrolment
- 323 participants (actual)
Sponsor and investigators
- Lead sponsor
- Johns Hopkins Bloomberg School of Public Health
- Sponsor type
- University, hospital or other
- Collaborators
- Fogarty International Center of the National Institute of Health, Arthur Davison Children's Hospital, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- Responsible party
- Sponsor
- Investigators
- Julie A Denison, PhD, Principal investigator, JHBSPHSam Miti, BSc HB, MBcHB, MeMMed-PEDS, Study director, Arthur Davison Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07221201
- Sponsor's protocol ID
- IRB00024597
- Other IDs
- 5R01TW012411-03
- Status last verified
- Jun 2026
- First submitted
- 24 Oct 2025
- Last updated
- 30 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The investigators will deposit data into an existing data repository for future research. After the study is completed, the de-identified, archived data will be transmitted to and stored in a Data Repository determined in consultation with the NIH Program Officer, for use by other researchers including those outside of the study. Blood samples will not be stored for future research purposes. De-identified archived data will be stored in a Data Repository. Study source documents (e.g. consent forms, attendance logs) will be retained for up to three years after data analysis is complete. There are no plans to store blood samples for future research. Blood samples drawn for viral load testing will be stored and disposed of according to MOH laboratory procedures.
Publications
Rahman A, Hamdani SU, Awan NR, Bryant RA, Dawson KS, Khan MF, Azeemi MM, Akhtar P, Nazir H, Chiumento A, Sijbrandij M, Wang D, Farooq S, van Ommeren M. Effect of a Multicomponent Behavioral Intervention in Adults Impaired by Psychological Distress in a Conflict-Affected Area of Pakistan: A Randomized Clinical Trial. JAMA. 2016 Dec 27;316(24):2609-2617. doi: 10.1001/jama.2016.17165.
PubMed 27837602Bryant RA, Schafer A, Dawson KS, Anjuri D, Mulili C, Ndogoni L, Koyiet P, Sijbrandij M, Ulate J, Harper Shehadeh M, Hadzi-Pavlovic D, van Ommeren M. Effectiveness of a brief behavioural intervention on psychological distress among women with a history of gender-based violence in urban Kenya: A randomised clinical trial. PLoS Med. 2017 Aug 15;14(8):e1002371. doi: 10.1371/journal.pmed.1002371. eCollection 2017 Aug.
PubMed 28809935Dawson KS, Watts S, Carswell K, Shehadeh MH, Jordans MJD, Bryant RA, Miller KE, Malik A, Brown FL, Servili C, van Ommeren M. Improving access to evidence-based interventions for young adolescents: Early Adolescent Skills for Emotions (EASE). World Psychiatry. 2019 Feb;18(1):105-107. doi: 10.1002/wps.20594. No abstract available.
PubMed 30600639Epping-Jordan JE, Harris R, Brown FL, Carswell K, Foley C, Garcia-Moreno C, Kogan C, van Ommeren M. Self-Help Plus (SH+): a new WHO stress management package. World Psychiatry. 2016 Oct;15(3):295-296. doi: 10.1002/wps.20355. No abstract available.
PubMed 27717271Merrill KG, Campbell JC, Decker MR, McGready J, Burke VM, Mwansa JK, Miti S, Frimpong C, Kennedy CE, Denison JA. Prevalence of physical and sexual violence and psychological abuse among adolescents and young adults living with HIV in Zambia. PLoS One. 2020 Jun 25;15(6):e0235203. doi: 10.1371/journal.pone.0235203. eCollection 2020.
PubMed 32584889Ayano G, Demelash S, Abraha M, Tsegay L. The prevalence of depression among adolescent with HIV/AIDS: a systematic review and meta-analysis. AIDS Res Ther. 2021 Apr 27;18(1):23. doi: 10.1186/s12981-021-00351-1.
PubMed 33906698Dow DE, Turner EL, Shayo AM, Mmbaga B, Cunningham CK, O'Donnell K. Evaluating mental health difficulties and associated outcomes among HIV-positive adolescents in Tanzania. AIDS Care. 2016 Jul;28(7):825-33. doi: 10.1080/09540121.2016.1139043. Epub 2016 Feb 3.
PubMed 26837437Boyes ME, Pantelic M, Casale M, Toska E, Newnham E, Cluver LD. Prospective associations between bullying victimisation, internalised stigma, and mental health in South African adolescents living with HIV. J Affect Disord. 2020 Nov 1;276:418-423. doi: 10.1016/j.jad.2020.07.101. Epub 2020 Jul 20.
PubMed 32871672Pantelic M, Shenderovich Y, Cluver L, Boyes M. Predictors of internalised HIV-related stigma: a systematic review of studies in sub-Saharan Africa. Health Psychol Rev. 2015;9(4):469-90. doi: 10.1080/17437199.2014.996243. Epub 2015 Apr 21.
PubMed 25559431Pantelic M, Boyes M, Cluver L, Thabeng M. 'They Say HIV is a Punishment from God or from Ancestors': Cross-Cultural Adaptation and Psychometric Assessment of an HIV Stigma Scale for South African Adolescents Living with HIV (ALHIV-SS). Child Indic Res. 2018;11(1):207-223. doi: 10.1007/s12187-016-9428-5. Epub 2016 Nov 23.
PubMed 29497463Earnshaw VA, Kidman RC, Violari A. Stigma, Depression, and Substance Use Problems Among Perinatally HIV-Infected Youth in South Africa. AIDS Behav. 2018 Dec;22(12):3892-3896. doi: 10.1007/s10461-018-2201-7.
PubMed 29909588Pantelic M, Boyes M, Cluver L, Meinck F. HIV, violence, blame and shame: pathways of risk to internalized HIV stigma among South African adolescents living with HIV. J Int AIDS Soc. 2017 Aug 21;20(1):21771. doi: 10.7448/IAS.20.1.21771.
PubMed 28853517Merrill KG, Campbell JC, Decker MR, McGready J, Burke VM, Mwansa JK, Miti S, Frimpong C, Kennedy CE, Denison JA. Past-Year Violence Victimization is Associated with Viral Load Failure Among HIV-Positive Adolescents and Young Adults. AIDS Behav. 2021 May;25(5):1373-1383. doi: 10.1007/s10461-020-02958-3.
PubMed 32761474Rongkavilit C, Wang B, Naar-King S, Bunupuradah T, Parsons JT, Panthong A, Koken JA, Saengcharnchai P, Phanuphak P. Motivational interviewing targeting risky sex in HIV-positive young Thai men who have sex with men. Arch Sex Behav. 2015 Feb;44(2):329-40. doi: 10.1007/s10508-014-0274-6. Epub 2014 Mar 26.
PubMed 24668304Pantelic M, Steinert JI, Park J, Mellors S, Murau F. 'Management of a spoiled identity': systematic review of interventions to address self-stigma among people living with and affected by HIV. BMJ Glob Health. 2019 Mar 19;4(2):e001285. doi: 10.1136/bmjgh-2018-001285. eCollection 2019.
PubMed 30997170
Study at a glance
From the registry record, last updated by the sponsor on 30 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Reducing the Intersecting Stigmas of HIV, Violence Victimization, and Mental Health: a Randomized Controlled Pilot Integrating Project YES! Youth Engaging for Success With WHO-Endorsed Mental Health Approaches Among Youth Living With HIV in Ndola, Zambia
- ClinicalTrials.gov ID
- NCT07221201
- Acronym / sponsor ID
- IRB00024597
- Conditions
- HIV - Human Immunodeficiency Virus, Mental Health, Anxiety, Depression in Adolescence, Stigma
- Keywords
- HIV, Adolescents, Caregivers, Africa, Youth, Intervention
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 323 participants (actual)
- Lead sponsor
- Johns Hopkins Bloomberg School of Public HealthUniversity, hospital or other
- Collaborators
- Fogarty International Center of the National Institute of Health, Arthur Davison Children's Hospital, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- Study start
- 25 Oct 2025 (actual)
- Primary completion
- 30 Jun 2026 (actual)
- Study completion
- 30 Jun 2026 (actual)
- First posted
- 27 Oct 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The proposed study will address the intersecting stigmas of HIV, violence and depression among adolescents and young adults (15-24) living with HIV (AYALHIV) in Zambia. The study will integrate a WHO-endorsed mental health approach into an existing HIV-stigma-reducing intervention, and refine measures of internalized and intersecting stigmas, to create and test the feasibility of Project YES+- a combined youth peer mentoring and lay mental health intervention. This research aims to shift HIV care and treatment for AYALHIV by addressing the multiple internalized and intersecting stigmas that impeded antiretroviral adherence and HIV viral suppression.
Detailed description
Nine out of ten AIDS-related deaths among adolescents occur in sub-Saharan Africa (SSA). Despite advances in antiretroviral combination therapy (ART), AIDS-related mortality among adolescents has only decreased 33% since 2010, compared to 66% among children. This slow decline in adolescent deaths is attributed in part to incomplete adherence to ART and subsequent viral failure. Only an estimated 34% of AYALHIV in Zambia, ages 15-24 years, have achieved viral suppression (<1000 copies/mL).
Stigma is increasingly recognized as a modifiable factor impacting ART adherence and viral suppression. Stigma as defined by Goffman is the social devaluation of a person due to an attribute discredited by society, with Parker and Aggleton critically examining stigma as a tool that reinforces inequalities. Different frameworks, such as the mental illness stigma framework and the HIV stigma framework, further delineate stigma into mechanisms experienced by people without the attribute, with the mechanisms being stereotypes, discrimination, and prejudice leading to social rejection, and those with the attribute, with the mechanisms being enacted (experienced), anticipated (beliefs about how others will treat you) and internalized stigma (accepting negative views and devaluing one's self) impacting physical, mental and social health. In this proposed research the investigators focus on internalized HIV stigma among AYALHIV, as well as internalized stigma related to the prevalent youth experiences of violence and depression. Further, the investigators also focus on intersectional stigma, capturing anticipated stigma associated with the complex reality of AYALHIV's multiple social identities instead of one specific attribute. This focus responds directly to this RFA and priority NIH/NIMH future directions for stigma-related research. Evidence shows that internalized stigma is related to viral failure and ART adherence among adults in SSA. Systematic review articles have also examined HIV-internalized stigma interventions; however, a 2019 systematic review of HIV self-stigma interventions in low- and middle-income countries found only one youth focused study from Thailand. In a more recent narrative review, two articles were AYALHIV specific, with only one measuring internalized stigma. In response to this distinct gap in stigma-reducing interventions, and informed by our team's preliminary studies, the investigators developed and tested Project YES! Youth Engaging for Success, to address internalized stigma and HIV outcomes among AYALHIV.
Project YES! is a peer-led facility-based youth mentoring program and is the only CDC evidence-based intervention (EBI) developed in SSA that reduced HIV-internalized stigma among AYALHIV ages 15-24. This RCT found that peer mentoring versus standard of care (SOC) decreased the relative odds of HIV-related internalized stigma (feelings of shame, guilt and worthlessness) by a factor of 0.39 (95% CI:0.21,0.73).) In a stratified analysis, intervention versus SOC participants from a pediatric clinic had a relative increase in the odds of viral suppression (VS) by a factor of 4.7 (95% CI:1.84, 11.78). However, study data also highlighted critical intervention gaps: 74% of AYALHIV experienced physical, sexual and/or emotional violence in the past year, with those experiencing violence at greater risk of viral failure (see preliminary studies).(17) Additionally, AYALHIV who screened positive for depression were less likely to achieve VS (53% vs 62%). Research among South African AYALHIV identified significant, multidirectional pathways linking HIV status and internalized stigma through violence victimization, depression and anticipated stigma, and mental health research clearly links internalized stigma with depression. Few studies, however, examined the relationship between internalized stigma and HIV outcomes, with one finding the impact of discrimination on reduced HIV care retention heightened by internalized stigma. With an estimated 25% of AYALHIV experiencing depression, and the high levels of violence in this population, the investigators must effectively intervene on these pathways to improve HIV outcomes during a developmental stage when youth are "developing and consolidating their sense of self".
To address these gaps the investigators propose integrating WHO-endorsed and lay delivered mental health approaches (e.g. PM+, SH+ and EASE) into our peer mentoring EBI (Project YES!) to create and test Project YES+. The World Health Organization, has various psychological management programs to address mental health conditions through lay workers. Examples of these mental health approaches include Project Management Plus (PM+) and Self Help+, both designed for adults 18+ years, and the Early Adolescent Skills for Emotions (EASE) program designed for young adolescents 10-14 years. While efficacious, the targeted age groups leave a clear gap in service options for 15-19 year olds. By adapting and integrating these mental health approaches into Project YES+, the investigators will specifically provide AYALHIV with problem-management skills through lay peer mentors shown to reduce depression and anxiety. The investigators hypothesize that Project YES+ will also reduce related internalized and intersecting stigmas and improve HIV outcomes. Our refinement of stigma measures will also advance the field's ability to test stigma-reducing interventions to disrupt the pathways among violence, depression, internalized stigma and HIV-related health outcomes. This proposed research will contribute to the field of HIV empirical research and care practices by refining measures and pilot testing a feasible peer led intervention designed to reduce stigma and achieve undetectable viral loads among AYALHIV 15-24 years of age.
STUDY DESIGN The development and pilot testing of Project YES+ will occur in two phases. Phase one has been completed and addressed Aim 1: to integrate an adapted WHO endorsed mental health intervention into Project YES! and Aim 2: to refine stigma measures. To achieve aim 1 the study team first worked with WHO to identify the most promising packages and components to adapt (e.g. PM+, SH+, EASE). After honing in on the key approaches, the investigators then held co-design workshops with AYA and caregivers to refine the Project YES+ To achieve Aim 2, to refine stigma measures, the team conducted cognitive interviewing with youth and caregivers. This phase 1 produced: 1) an age-and-culturally relevant AYALHIV stigma reduction intervention linked to mental health and HIV outcomes, and 2) adapted measures of intersectional, violence-, and depression-related stigmas for AYALHIV.
Phase two is the focus of this registration with clinicaltrials.gov. For phase two, the study team will address Aim 3: to pilot test the intervention, collecting pilot Project YES+ outcomes by conducting an RCT with 50 intervention and 50 comparison AYALHIV and their caregivers who attend HIV care at the Arthur Davison Children's Hospital (ADCH) in Ndola, Zambia (expanding to other clinics if needed to reach the sample size). Individual-level AYA study measures, including stigma, depression, violence, ART adherence, and blood draws for viral testing, will occur at baseline and endline. This data will advance our knowledge on stigma measures and the integration of mental health care in an effective HIV stigma reducing intervention to address the bi-directional associations among HIV, depression, violence victimization, and various internalized stigmas. This data will provide the foundation for a future impact study of Project YES+ on AYALHIV stigmas and HIV outcomes. The specific aim 3 is detailed below:
Aim 3: The purpose of Aim 3 is to test the feasibility of conducting Project YES+ among AYALHIV to prepare preliminary evidence and working knowledge to test the intervention impact in the future. To assess whether 90% of AYAHLIV will attend at least 80% of the intervention sessions with a 90% confidence interval and a margin of error + 10, the investigators will need a minimum sample size of 25 AYALHIV in each study arm. A group sample size of 50 though, will allow us to achieve 74% power to detect a two-sided difference with an alpha of 0.05 of 25 points between the two groups on internalized stigma related to HIV, violence or depression. The investigators know from Project YES! data that a reduction of this size in HIV-internalized stigma is possible. In addition, this sample size will provide valuable data on the proportion of participants reducing psychological distress. At baseline 100% of all AYALHIV participants will have have a positive screen for the Kessler 6 measure of psychological distress and the investigators assume some variability in the proportion with a positive Kessler 6 score in the control group at endline. Group sizes of 50 will achieve 80% power to detect a 20% difference in the Kessler 6 from 95% to 75% between the control and intervention group for a two-sided comparison with alpha=0.05.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Randomized Controlled Trial (Individual Level)
| Arm | Type | Receives |
|---|---|---|
| Standard of Care | No intervention | –The comparison group will receive the standard of care. Standard of care at ADCH includes an optional monthly AYALHIV youth group. The comparison arm participants will also be offered referrals to health care providers if they screen positive for depression or have experienced severe forms of violence (a process the investigators utilized and refined during the Project YES! study). |
| Project YES+ intervention arm | Experimental | Behavioral: Project YES+ intervention armProject YES+ will be about 4 months and will consist of an orientation meeting with the youth client, their caregiver, the healthcare worker and the youth peer mentor to introduce the intervention. Youth clients will then meet with their YPM individually and in groups with other youth living with HIV in the intervention, and go through the WHO- Self Help plus group meetings. Caregivers will also attend three different caregiver group meetings. At the end, there will be a transition group meeting with youth and caregivers together, followed by one last individual mentoring meeting with the youth. All individual and group meetings are facilitated by the youth peer mentor. Study team members will provide reminder calls for youth and their caregivers before intervention meetings and data collection points. |
Who may qualify
- Ages
- 15 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (12 listed)
- For youth
- Be between ages 15-21
- living within 30-minutes, by personal transportation, of the clinic by self-report,
- and being available to attend sessions and data collection over a 4-8 month time period On ART for at least 6 months
- On first-line ART
Key exclusion criteria (3 listed)
- For youth,
- only one youth per household may join.
- Also participants will be excluded from joining the RCT if they are at imminent risk of suicide based on WHO guidance on the Self Help plus program.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Project YES+ intervention armProject YES+ integrates Project YES! | Behavioural | Project YES+ intervention arm |
Primary outcome
Feasibility of intervention as assessed by percentage of sessions attended
Time frame: Up to 4 months
Feasibility of 90% of AYAHLIV attending at least 80% of the intervention sessions with a 90% confidence interval and a margin of error + 10.
Number of intervention participants who report they would recommend Project YES+ to their peers
Time frame: up to 4 months
The endline question is "Overall, you would recommend/not recommend this program to another youth living with HIV" with the response options would recommend, would not recomment, decline to answer"
Number of intervention participants who would recommend Project YES+ for caregivers
Time frame: up to four months
This outcome will be assessed during endline with the question "Overall, you would recommend/not recommend this program to a caregiver of a another youth living with HIV"
1 secondary outcome
Number of youth participants with a positive composite score consisting of psychological distress (Kessler 6) and one positive stigma score (internalized, violence, mental health and intersectional stigma).
Time frame: Baseline up to approximately 4 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jun 2026.
- Background: PubMed 27837602Rahman A, Hamdani SU, Awan NR, Bryant RA, Dawson KS, Khan MF, Azeemi MM, Akhtar P, Nazir H, Chiumento A, Sijbrandij M, Wang D, Farooq S, van Ommeren M. Effect of a Multicomponent Behavioral Intervention in Adults Impaired by Psychological Distress in a Conflict-Affected Area of Pakistan: A Randomized Clinical Trial. JAMA. 2016 Dec 27;316(24):2609-2617. doi: 10.1001/jama.2016.17165.
- Background: PubMed 28809935Bryant RA, Schafer A, Dawson KS, Anjuri D, Mulili C, Ndogoni L, Koyiet P, Sijbrandij M, Ulate J, Harper Shehadeh M, Hadzi-Pavlovic D, van Ommeren M. Effectiveness of a brief behavioural intervention on psychological distress among women with a history of gender-based violence in urban Kenya: A randomised clinical trial. PLoS Med. 2017 Aug 15;14(8):e1002371. doi: 10.1371/journal.pmed.1002371. eCollection 2017 Aug.
- Background: PubMed 30600639Dawson KS, Watts S, Carswell K, Shehadeh MH, Jordans MJD, Bryant RA, Miller KE, Malik A, Brown FL, Servili C, van Ommeren M. Improving access to evidence-based interventions for young adolescents: Early Adolescent Skills for Emotions (EASE). World Psychiatry. 2019 Feb;18(1):105-107. doi: 10.1002/wps.20594. No abstract available.
- Background: PubMed 27717271Epping-Jordan JE, Harris R, Brown FL, Carswell K, Foley C, Garcia-Moreno C, Kogan C, van Ommeren M. Self-Help Plus (SH+): a new WHO stress management package. World Psychiatry. 2016 Oct;15(3):295-296. doi: 10.1002/wps.20355. No abstract available.
- Background: PubMed 32584889Merrill KG, Campbell JC, Decker MR, McGready J, Burke VM, Mwansa JK, Miti S, Frimpong C, Kennedy CE, Denison JA. Prevalence of physical and sexual violence and psychological abuse among adolescents and young adults living with HIV in Zambia. PLoS One. 2020 Jun 25;15(6):e0235203. doi: 10.1371/journal.pone.0235203. eCollection 2020.
- Background: PubMed 33906698Ayano G, Demelash S, Abraha M, Tsegay L. The prevalence of depression among adolescent with HIV/AIDS: a systematic review and meta-analysis. AIDS Res Ther. 2021 Apr 27;18(1):23. doi: 10.1186/s12981-021-00351-1.
- Background: PubMed 26837437Dow DE, Turner EL, Shayo AM, Mmbaga B, Cunningham CK, O'Donnell K. Evaluating mental health difficulties and associated outcomes among HIV-positive adolescents in Tanzania. AIDS Care. 2016 Jul;28(7):825-33. doi: 10.1080/09540121.2016.1139043. Epub 2016 Feb 3.
- Background: PubMed 32871672Boyes ME, Pantelic M, Casale M, Toska E, Newnham E, Cluver LD. Prospective associations between bullying victimisation, internalised stigma, and mental health in South African adolescents living with HIV. J Affect Disord. 2020 Nov 1;276:418-423. doi: 10.1016/j.jad.2020.07.101. Epub 2020 Jul 20.
- Background: PubMed 25559431Pantelic M, Shenderovich Y, Cluver L, Boyes M. Predictors of internalised HIV-related stigma: a systematic review of studies in sub-Saharan Africa. Health Psychol Rev. 2015;9(4):469-90. doi: 10.1080/17437199.2014.996243. Epub 2015 Apr 21.
- Background: PubMed 29497463Pantelic M, Boyes M, Cluver L, Thabeng M. 'They Say HIV is a Punishment from God or from Ancestors': Cross-Cultural Adaptation and Psychometric Assessment of an HIV Stigma Scale for South African Adolescents Living with HIV (ALHIV-SS). Child Indic Res. 2018;11(1):207-223. doi: 10.1007/s12187-016-9428-5. Epub 2016 Nov 23.
- Background: PubMed 29909588Earnshaw VA, Kidman RC, Violari A. Stigma, Depression, and Substance Use Problems Among Perinatally HIV-Infected Youth in South Africa. AIDS Behav. 2018 Dec;22(12):3892-3896. doi: 10.1007/s10461-018-2201-7.
- Background: PubMed 28853517Pantelic M, Boyes M, Cluver L, Meinck F. HIV, violence, blame and shame: pathways of risk to internalized HIV stigma among South African adolescents living with HIV. J Int AIDS Soc. 2017 Aug 21;20(1):21771. doi: 10.7448/IAS.20.1.21771.
- Reference 1Link provided by the sponsor.
- Reference 2Link provided by the sponsor.
- Reference 3Link provided by the sponsor.
- Reference 27Link provided by the sponsor.
- Individual participant dataSharing planned: Yes. The investigators will deposit data into an existing data repository for future research. After the study is completed, the de-identified, archived data will be transmitted to and stored in a Data Repository determined in consultation with the NIH Program Officer, for use by other researchers including those outside of the study. Blood samples will not be stored for future research purposes. De-identified archived data will be stored in a Data Repository. Study source documents (e.g. consent forms, attendance logs) will be retained for up to three years after data analysis is complete. There are no plans to store blood samples for future research. Blood samples drawn for viral load testing will be stored and disposed of according to MOH laboratory procedures.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Julie A Denison, PhD principal investigator
JHBSPH
Sam Miti, BSc HB, MBcHB, MeMMed-PEDS study director
Arthur Davison Children's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Project YES+ intervention arm in people with HIV - Human Immunodeficiency Virus and Mental Health, run by Johns Hopkins Bloomberg School of Public Health at 1 site in Zambia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 12 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 30 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Zambia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Feasibility of intervention as assessed by percentage of sessions attended (time frame: Up to 4 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07221201, which also lists 26 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jun 2026.