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Behavioural Intervention
iEngage Social Network Intervention for HIV/AIDS
N/A
Waitlist Available
Led By Tiarney Ritchwood, Ph.D.
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6 month, and 12 month follow up
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a social network intervention to improve HIV-related outcomes for ALWH in South Africa.
Who is the study for?
This trial is for adolescents living with HIV in South Africa who are willing to let researchers access their clinic data, live in the study area, and can consent or bring a social network member to join the intervention.
What is being tested?
The 'iEngage' intervention is being tested to see if it improves retention in HIV care and antiretroviral therapy adherence among adolescents by leveraging social support within their networks.
What are the potential side effects?
Since 'iEngage' focuses on social support rather than medication, there may not be direct medical side effects. However, participants might experience emotional or psychological impacts from engaging with their social networks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 6 month, and 12 month follow up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 month, and 12 month follow up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Acceptability: exit interviews
Feasibility: exit interviews
Secondary study objectives
Change in ART adherence
Change in HIV knowledge
Change in HIV stigma & discrimination
+18 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: iEngageExperimental Treatment1 Intervention
The intervention is a network-based, social support intervention to improve ALWH retention in HIV care and ART adherence. The specific intervention will be developed during Aim 2 of the study and uses qualitative findings, along with data from Aim 1, to develop an interventions that integrates participant feedback and borrows components from two existing interventions
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Who is running the clinical trial?
Wake Forest University Health SciencesLead Sponsor
1,390 Previous Clinical Trials
2,546,605 Total Patients Enrolled
Duke UniversityLead Sponsor
2,451 Previous Clinical Trials
3,067,040 Total Patients Enrolled
National Institute of Mental Health (NIMH)NIH
2,907 Previous Clinical Trials
2,738,899 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- N/A
Research Study Groups:
This trial has the following groups:- Group 1: iEngage
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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