跳至主要内容
临床试验/NCT06770101
NCT06770101招募中不适用

Suicide Assessment and Feasible Evidence-based Treatments for Youth Living With HIV in Lilongwe: SAFETY Planning Pilot Trial

University of Pennsylvania4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
4
主要终点
Study retention (study feasibility)

研究概览

简要总结

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.

详细描述

This project aims to evaluate the feasibility, acceptability, fidelity, and preliminary effectiveness of the enhanced Friendship Bench+Safety Planning (FB+SP) intervention model. We will enroll 60 depressed ALWH who report suicidality from four facilities in Lilongwe, Malawi, and randomize them 1:1 to the enhanced FB+SP model or augmented usual care. This pilot trial is a step toward our long-term goal of generating and implementing an evidence-based model to prevent suicide in Malawi amongst ALWH by enhancing the capacity of the health system to identify suicidality and provide evidence-based care. Information gathered in this proposal will be used to develop a subsequent randomized control trial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
13 Years 至 19 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 13-19
  • •Diagnosed with HIV
  • •Report current or historical suicidal ideation and behaviors (SIBs) on question 9 of the Patient Health Questionnaire modified for adolescents (PHQ-9-A) and the Ask Suicide-Screening questionnaire (ASQ)
  • •Living in the clinic's catchment area with intention to remain for more than 1 year
  • •Willing to provide consent (age 18+ or 16-17 years old and married and thereby considered emancipated minors per Malawi law) or assent with parental consent (age 13-17).

排除标准

  • •Refuse to participate
  • •Refuse to be audio-taped for in-depth interviews

研究组 & 干预措施

Augmented Usual Care

Active Comparator

Continue with usual outpatient care, augmented to provide mental health evaluation, brief supportive counseling, information, education and support on SIBs, and (if indicated) facilitation of referral to the clinic's psychiatric nurse or to Bwaila Hospital.

干预措施: Augmented usual care (Behavioral)

Enhanced Friendship Bench + Safety Planning (FB+SP)

Experimental

Friendship Bench (FB) problem-solving therapy and Safety Planning (SP)

干预措施: Behavioral: Enhanced Friendship Bench + Safety Planning (Behavioral)

结局指标

主要结局

Study retention (study feasibility)

时间窗: Through study completion- 6 months

This outcome measure of feasibility will be measured as the ability to retain ALWH in the pilot trial. Feasibility will be evaluated by measuring the number of participants retained in the study (number of patients enrolled at baseline who are still enrolled in the trial) through study completion.

Recruitment rate (Intervention feasibility)

时间窗: Baseline

This outcome measure of feasibility will be measured as the ability to successfully enroll ALWH in the pilot trial. Feasibility will be evaluated by measuring the recruitment rate (number of patients approached in order to accrue the final sample).

Overall satisfaction with the intervention among participants (intervention acceptability)

时间窗: 6 months

The proportion of participants who found the intervention acceptable and helpful among all participants who received the intervention.

Proportion of sessions meeting fidelity threshold (intervention fidelity)

时间窗: 6 months

The proportion of sessions meeting or exceeding expectations for at least 80% of the total number of fidelity checklist items assessed per session during random monitoring sessions out of all sessions monitored.

次要结局

  • Prevalence of suicidal ideation and behaviors(6 months)
  • Prevalence of suicide risk(6 months)
  • Prevalence of depressive symptoms(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Melissa Stockton

Assistant Professor of Psychiatry

University of Pennsylvania

研究点 (4)

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