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临床试验/NCT03031197
NCT03031197已完成不适用

The Supporting Adolescent Adherence in Vietnam (SAAV) Study

University of New England1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2017年5月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
81
试验地点
1
主要终点
Optimal on-time adherence

研究概览

简要总结

The small RCT will assess feasibility, acceptability, and impact of a real-time intervention on ART adherence and clinical outcomes for HIV-positive adolescents. All subjects will use a wireless pill container (WPC) to monitor adherence. Intervention subjects will receive a personalized triggered reminder (cellphone message/call or bottle-based flash/alarm) when they miss a dose, and engage in monthly counseling sessions informed by their adherence data. Comparison subjects will receive usual care and an offer of counseling at monthly clinic visits.

详细描述

A major priority in HIV care and treatment is identifying effective interventions for adolescent patients, including those that make use of new technologies, to help them achieve and maintain high levels of adherence to antiretroviral treatment (ART), particularly as they take responsibility for their own medication-taking in the transition to adult care. The research planned here will contribute to the scientific evidence base on approaches to support ART adherence effectively among youth by 1) conducting formative research on adherence challenges among adolescents and refining options for a personalized adherence intervention package; and 2) implementing a small randomized controlled trial (RCT) to assess the feasibility, acceptability, and efficacy of a novel real-time feedback intervention that permits adolescent patients to tailor intervention features to suit their individual preferences.

研究设计

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

盲法说明

Open Label

入排标准

年龄范围
12 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •currently a patient at the Infectious Disease (ID) clinic at National Hospital for Pediatrics (NHP) in Hanoi, Vietnam
  • •between 12 and 17 years old of age AND
  • •expected to remain in care at the NHP for 7 months minimum
  • •currently on ART
  • •live in the clinic catchment area
  • •willing to provide informed assent, caregiver willing to provide consent
  • •identified ás having adherence challenges (CD4, detectable VL, and/or clinician suggestion)

排除标准

  • •below the age of 12 years or above the age of 18
  • •not currently on ART
  • •live outside the clinic catchment area
  • •not willing to provide informed assent, caregiver not willing to provide consent

研究组 & 干预措施

Tailored realtime triggered reminder pkg

Experimental

The core intervention will utilize innovative wireless technology to provide patients with 1) real time, personalized wireless reminder messages when ART doses are not taken on time, and 2) 'feedback' on adherence behavior via monthly interactive counseling sessions informed by summaries of their previous month's behavior. The core intervention will be personalized by each intervention arm patient, who may choose features to suit their preferences.

干预措施: Tailored realtime triggered reminder pkg (Combination Product)

Control

No Intervention

Comparison subjects will receive usual care and an offer of counseling at monthly clinic visits.

结局指标

主要结局

Optimal on-time adherence

时间窗: End of intervention period (month 7)

Proportion of patients with ≥95% on-time adherence at end of 6-month intervention period in each study arm

次要结局

  • CD4 count(Pre-intervention month (month 1) vs. last intervention month (month 7))
  • Viral load(End of intervention period (month 7))

研究者

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

Mary DeSilva

Assistant Research Professor

University of New England

研究点 (1)

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