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临床试验/NCT07754994
NCT07754994尚未招募不适用

Remote Hypertension Medication Self-Management Technology for Older Adults

University of Illinois at Urbana-Champaign0 个研究点目标入组 40 人开始时间: 2026年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
主要终点
Change in Self-regulation Measured by Adapted Short Self-Regulation Questionnaire (SSRQ)

研究概览

简要总结

The goal of this feasibility study is to evaluate the preliminary impact of a mobile health application (app) called bpMedManage-R, designed to support hypertension medication self-management in persons with mild cognitive impairment (PwMCI) who live alone. The main questions this study aims to answer are whether the bpMedManage-R app shows preliminary impact on medication-related self-regulation (the ability to consistently take medications as prescribed) and self-efficacy (confidence in independently managing medication use). Participants will be randomized after a baseline assessment to the bpMedManage-R Immediate Group or the bpMedManage-R Delayed Group. Participants assigned to the Immediate Group will complete a 4-week baseline adherence period, at the end of which they will enter the intervention phase. A remote training session will be conducted to initiate the intervention phase, during which participants will download the app, learn to use it, and set up their medication schedule and reminders within the app with support from the study team. They will then use the app for 8 weeks to self-manage their medications, take part in brief weekly check-ins to review progress, and complete Outcome Assessment 1 at the end of the 8-week intervention phase. Participants assigned to the Delayed Group will complete a 12-week baseline adherence period, at the end of which they will complete Outcome Assessment 1. Subsequently, they will enter the intervention phase and will follow a process similar to that of the Immediate Group. At the end of the 8-week intervention phase, they will complete Outcome Assessment 2. Researchers will compare participants who receive the bpMedManage-R app intervention immediately to those assigned to the delayed control group.

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
Single (Participant)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Fluent in English
  • Adequate visual and auditory acuity
  • Community dwelling
  • Lives alone
  • Self-reported memory problems
  • Manage at least one hypertension medication
  • Passing score on Telephone Interview for Cognitive Status - Modified (TICS- M) between 27-37
  • Passing score on Montreal Cognitive Assessment (MoCA) between 20 and 26
  • Geriatric Depression Scale (GDS) score of 6 or lower
  • Stated willingness to comply with all study procedures and availability for the duration of the study

排除标准

  • Diagnosis of dementia
  • Major communication difficulties

结局指标

主要结局

Change in Self-regulation Measured by Adapted Short Self-Regulation Questionnaire (SSRQ)

时间窗: Immediate Group: Baseline; 8 weeks post-intervention Delayed Group: Baseline; 8 weeks post wait-list period; 8 weeks post-intervention

A 31-item measure of the ability to regulate behavior in order to achieve desired future outcomes.

Change in Medication Usage Self-efficacy Measured by Medication Usage Self-Efficacy (MUSE) questionnaire

时间窗: Immediate Group: Baseline; 8 weeks post-intervention Delayed Group: Baseline; 8 weeks post wait-list period; 8 weeks post-intervention

A brief 8-item tool that measures how confident a person is in understanding and taking their prescribed medications.

Change in Medication Usage Self-efficacy Measured by Medication Adherence Self-Efficacy Scale-revised (MASES-R)

时间窗: Immediate Group: Baseline; 8 weeks post-intervention Delayed Group: Baseline; 8 weeks post wait-list period; 8 weeks post-intervention

A13-item questionnaire that measures a person's confidence in taking their medication even when faced with difficult situations.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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