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Clinical Trials/NCT03076996
NCT03076996
Completed
Not Applicable

Youth Power Action Feasibility Study of Online Support Group Intervention Among Adolescents Living With HIV in Nigeria

FHI 3601 site in 1 country41 target enrollmentJune 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV/AIDS
Sponsor
FHI 360
Enrollment
41
Locations
1
Primary Endpoint
Percentage of Active Members Who Have at Least One Post in Group Chat Session.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study will examine the feasibility and acceptability of an intervention designed to improve retention in HIV care services and improve anti-retroviral therapy (ART) adherence among adolescents ages 15-19 years living with HIV enrolled in ART services.

Detailed Description

Study aim is to examine the feasibility and acceptability of an intervention designed to improve retention in HIV care services and improve anti-retroviral therapy (ART) adherence among adolescents ages 15-19 years living with HIV enrolled in ART services. A single group, pre/posttest design including structured questionnaires with adolescents living with HIV. Additionally, we will abstract clinical data from the medical record system. We will also conduct in-depth interviews with a subset of participants, as well as health care staff who are engaged in the intervention, at endline. The objectives of this study are: 1. To examine the feasibility of implementing a mobile/electronic health (m/eHealth) intervention designed to improve retention in HIV care services and ART adherence among ALHIV ages 15-19 years through an online support group (using Facebook). 2. To assess acceptability of and engagement in the intervention by the target audience to inform improvements to the intervention. 3. To gather preliminary data on the psycho-social and health-related outcomes that the intervention is designed to affect to inform an outcome evaluation study that will be conducted following the conclusion of the feasibility study. 4. To collect information on recruitment, informed consent and data collection processes to inform the outcome evaluation study of the current intervention that will be conducted once findings from this feasibility study are incorporated into the intervention design.

Registry
clinicaltrials.gov
Start Date
June 1, 2017
End Date
January 15, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
FHI 360
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • HIV positive and currently on ART for at least 6 months
  • Age 15 to 19 years
  • Can demonstrate basic literacy necessary to participate in online chats

Exclusion Criteria

  • Not planning to remain in the study area (within Akwa Ibom State) for the duration of the study (approximately 6 months)
  • Currently enrolled in an in-person support group
  • Currently enrolled in another research study related to HIV service retention or ART adherence
  • Critically or severely ill requiring hospitalization or such that the individual is unable to provide informed consent at the time of study recruitment

Outcomes

Primary Outcomes

Percentage of Active Members Who Have at Least One Post in Group Chat Session.

Time Frame: 3 months

Participants level of engagement in support group activities informs on the feasibility of intervention, measured by percentage of active members who have at least one post in group chat session.

Secondary Outcomes

  • Acceptability Score(3 months)
  • Adherence to ART as Measured by the AACTG Adherence Assessment(3 months)
  • Adherence to Follow-up Visit Within 1 Month of Scheduled Date(3 months)

Study Sites (1)

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