NCT01291485已完成不适用
Randomized Clinical Trial Examining the Efficacy of an Electronic Intervention for HIV Medication Adherence
Oklahoma State University Center for Health Sciences2 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2011年1月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 97
- 试验地点
- 2
- 主要终点
- HIV medication adherence
研究概览
简要总结
The purpose of this study is to develop and examine the feasibility and initial efficacy of a computer-based intervention to improve medication adherence among people living with HIV.
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •infected with HIV
- •over age 18
- •currently prescribed a Highly Active Antiretroviral Therapy (HAART) regimen
- •prescribed a regimen for the first time, changing regimens, or report adherence below 95% agree to brief follow-up interviews
排除标准
- •physical impairment that would prevent them from successfully completing the computer-based program (e.g., blind, deaf, severe neuropsychological impairment)
- •Actively psychotic
- •Not fluent in English
结局指标
主要结局
HIV medication adherence
时间窗: up to 6 months
Self-reported adherence to HIV medications will be assessed using the AACTG Medication Adherence Questionnaire (M. A. Chesney, et al., 2000).
次要结局
- HIV Treatment Adherence Self-Efficacy(Baseline, 1-month, 3 months, and 6-months)
- Quality of Life(Baseline, 1-month, 3-months, and 6-months)
- Viral Load(Baseline, 1 month, 3 months, and 6 months)
- CD4 cell count(Baseline, 1 month, 3 months, and 6 months)
研究者
Kasey Claborn
Doctoral Candidate
Oklahoma State University Center for Health Sciences
研究点 (2)
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