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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05938803
Other study ID # R01MH131414
Secondary ID R01MH131414
Status Recruiting
Phase N/A
First received
Last updated
Start date September 22, 2023
Est. completion date January 31, 2027

Study information

Verified date May 2024
Source Harvard University Faculty of Medicine
Contact Alyson Nunez
Phone 617-432-5224
Email alyson_nunez@hms.harvard.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is an evaluation of an intervention (nicknamed "PASEO") that aims to facilitate the transition to adult HIV care for adolescents living with HIV in Lima, Peru. The intervention consists of health systems navigation and accompaniment, monthly check-ins with a lay health worker, enhanced social support provided through peer support groups, education sessions, mental health screening and referral, resolution of acute needs, and individualized adherence support. The study is a two-arm 1:1 randomized evaluation to determine the short- and long-term (i.e., post-intervention) efficacy of the PASEO intervention with regard to retention with viral load suppression as well as other indicators of well-being. The cumulative incidence of unsuccessful transition at 12- and 24-months will be compared. The cost and cost-effectiveness of the study intervention in terms of cost per additional successful transition achieved will be estimated. Data on implementation considerations essential for uptake, sustainability, and successful adoption by the public sector will be provided.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date January 31, 2027
Est. primary completion date November 30, 2026
Accepts healthy volunteers No
Gender All
Age group 15 Years to 23 Years
Eligibility Inclusion Criteria: - Adolescent or young person living with HIV and aware of diagnosis - 15 to 21 years of age (may be increased to 23 to meet recruitment targets) - Currently taking or eligible for ART at a participating facility - Scheduled to transition to adult care or previous unsuccessful transition to adult care - Willing to participate regardless of the study arm to which they will be assigned - Able and willing to provide written informed consent Exclusion Criteria: - Living outside of Lima province - Participation in the PASEO pilot study - Current enrollment in another research study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
PASEO
The intervention consists of community-based accompaniment intervention aimed at facilitating the transition to adult HIV care for adolescents living with HIV in Lima, Peru.The intervention includes the following activities: health systems navigation and accompaniment to clinic visits, monthly check-ins with an entry-level health worker, social support provided through peer support groups, education sessions, resolution of acute needs, and individualized adherence support.

Locations

Country Name City State
Peru Instituto Nacional de Salud del Nino Breña Lima
Peru Hospital Nacional Daniel Alcides Carrión Callao Lima
Peru Hospital Nacional Arzobispo Loayza Lima
Peru Hospital Nacional Hipólito Unanue Lima

Sponsors (2)

Lead Sponsor Collaborator
Harvard University Faculty of Medicine National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

Peru, 

Outcome

Type Measure Description Time frame Safety issue
Primary Unsuccessful transition Number of people who experience death, loss to follow-up or unsuppressed viral load >200 copies/mL 12 months
Primary Unsuccessful transition Number of people who experience death, loss to follow-up or unsuppressed viral load >200 copies/mL 24 months
Secondary HIV-related death or loss to follow-up Time to HIV-related death or loss to follow-up within 12 and 24 months
Secondary Clinic visit attendance Number of scheduled visits attended, among those retained 12 and 24 months
Secondary CD4 cell count Change in CD4 cell count from baseline 12 and 24 months
Secondary Self-efficacy Change in self-efficacy (assessed using the NIH toolbox) from baseline 6, 9, 12, 24 months
Secondary Transition readiness Change in transition readiness (assessed using the Am I on TRAC and Got Transitions questionnaires) from baseline 6, 9, 12, 24 months
Secondary Perceived social support Change in social support (assessed using the NIH toolbox) from baseline 6, 9, 12, 24 months
Secondary HIV-related stigma Change in HIV-related stigma (assessed using an Abbreviated Berger HIV Stigma Scale: score range 21-84, higher score indicating greater levels of stigma) from baseline 6, 9, 12, 24 months
Secondary Social Connectedness Change in social connectedness (assessed using the Social Connectedness Scale: score range 20-120, higher score indicating greater sense of social connectedness and belongingness) from baseline 6, 9, 12, 24 months
Secondary Sexual Behavior Change in sexual behavior of risk (assessed using questions from the Youth Risk Behavior Surveillance System) from baseline 6, 9, 12, 24 months
Secondary ART Adherence Change in percentage of days, during the last 30, during which at least one dose was missed (assessed using a 30 day-recall) from baseline. Minimum= -100, maximum=100; scores above 0 indicate an improvement relative to baseline, with higher scores indicating greater improvements. Assessed among those on treatment for at least a month at enrollment. 6, 9, 12, 24 months
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