A Social Media Intervention to Improve Retention in Care for Adolescents and Young Adults With HIV in Uganda

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15+
SponsorMbarara University of Science and Technology

About this trial

Adolescents and young adults with HIV (AYWH) aged 15- 24 years are the fastest-growing population of people living with HIV worldwide. AYWH have worse outcomes along the HIV continuum of care than adults with HIV; HIV/AIDS is the second leading cause of mortality and the fourth leading cause of disability among AYWH worldwide. This study will develop a youth-friendly, mobile health (mHealth) intervention to improve retention in care that has the potential to improve AIDS-related mortality and morbidity among AYWH and decrease onward new transmission, thus contributing towards ending the HIV/AIDS pandemic.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

AYWH who are aged 15-24

AYWH who are new to care (less than or equal to one month in care), or who are re-engaging in care after being lost to follow up for greater or equal to six months.

Fluent in English or Runyankole (the local language)

For aim 3, AYWH who have access (own or shared) to a smartphone

Disqualifiers

Clinic counsellors who are ≥18 years

Clinic counsellors who have worked at the HIV clinic for ≥ 1 year

Trial design

Design model

Parallel

Treatments tested in this trial

  • A social media based intervention

    Behavioral

    WatsApp-based modules to influence retention in care behaviour

Treatment groups

105 Participants
are divided into 2 treatment groups
Group A: Intervention armExperimental treatment 1 intervention
Group B: Wait list control armNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

The primary intervention outcome will be the acceptability, feasibility of the intervention.

Acceptability will be measured using the Acceptability of Intervention Measure (AIM) and will be considered acceptable if ≥70% (35/50) of intervention participants rate all 4 items on the AIM (a 5-point Likert scale) as "agree" or higher. The intervention will be considered feasible if ≥70% (35/50) of intervention participants rate all 4 items on the Feasibility of Intervention Measure (FIM), (a 5-point Likert scale) as "agree" or higher.

Time frame
12 months

Secondary outcomes

1

Retention

The secondary outcome of the intervention will be retention in care, which will be assessed at the end of 12 months. This will be defined as the proportion of participants active in care (i.e have not missed a scheduled appointment in the last 12 months) The investigators will compare the proportion of participants actively engaged in care in the immediate intervention and the deferred intervention arm.

Time frame
12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Mbarara University of Science and Technology

Lead sponsor

Fogarty International Center of the National Institute of Health

Collaborator