Actively Recruiting

Phase Not Applicable
Age: 13Years - 19Years
All Genders
NCT06770101

Suicide Assessment and Feasible Evidence-based Treatments for Youth Living With HIV in Lilongwe

Led by University of Pennsylvania · Updated on 2025-10-08

60

Participants Needed

4

Research Sites

63 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overall aim of this study is to determine the feasibility, fidelity, acceptability, and preliminary effectiveness of the Friendship Bench +Safety Planning intervention in reducing suicidal ideation and behaviors (SIBs) and improving HIV engagement amongst adolescents living with HIV (ALWH) when compared to augmented usual care.

CONDITIONS

Official Title

Suicide Assessment and Feasible Evidence-based Treatments for Youth Living With HIV in Lilongwe

Who Can Participate

Age: 13Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 13 to 19 years
  • Diagnosed with HIV
  • Report current or past suicidal thoughts or behaviors on specific screening questionnaires
  • Living in the clinic's area with plans to remain for more than one year
  • Willing to give consent (if 18 or older) or assent with parental consent (if 13-17 years old and not emancipated)
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Refusal to be audio-recorded for in-depth interviews

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Area 18 Health Center

Lilongwe, Malawi

Actively Recruiting

2

Area 25 Health Center

Lilongwe, Malawi

Actively Recruiting

3

Kawale Health Center

Lilongwe, Malawi

Actively Recruiting

4

Lighthouse Health Center

Lilongwe, Malawi

Actively Recruiting

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Research Team

M

Melissa Stockton, PhD

CONTACT

K

Kazione Kulisewa, MBBS MMed

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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