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临床试验/NCT06415617
NCT06415617已完成不适用

Effects of A Home-based Psychoeducation Programme on Subjective Well-being for Older Adults With Frailty in the Community: A Feasibility Trial

TAO An1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年11月24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
24
试验地点
1
主要终点
Participation rate, self-reported intervention adherence, and attrition rate.

研究概览

简要总结

This study aims to test the feasibility and acceptability of home-based psychoeducation in older adults with frailty in the community. The main questions it aims to answer are

  1. Are the proposed eligibility criteria for participants and the study process in recruiting and retaining the participants appropriate?
  2. Is home-based psychoeducation feasible and acceptable for older adults with frailty in the community?

Participants will receive 12 weekly online group-based sessions at their homes. The content for the experimental group and control group is different:

  • Intervention group: psychoeducation
  • Control group: physical health education

Participants will receive two home visits for data collection. An individual interview will be conducted with participants in the experimental group to explore their experiences.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • (1) aged 65 years or over; (2) meeting frailty criteria by FRAIL scale (score 3 or above) ; (3) mentally competent screened by The Abbreviated Mental Test (AMT≥6) ; (4) able to speak and understand Cantonese; (5) living at home; (6) having experience using a smartphone (e.g.: sending messages, watching videos)

排除标准

  • (1) have a visual or hearing problem or a language barrier that may affect their communication or understanding; (2) being unfit for home-based exercise, as defined by having one point or above at either the 25-item Home Falls and Accidents self-reported screening tool (HOME-FAST), which is a comprehensive tool for identify home hazards for fall (3) are currently practising exercise for at least 150 minutes per week in previous four weeks; (4) are receiving active psychiatric or antidepressant treatment or joining other physical exercises or rehabilitation programmes

结局指标

主要结局

Participation rate, self-reported intervention adherence, and attrition rate.

时间窗: 12 weeks post-allocation

The feasibility of the study will be measured in terms of participation rate, self-reported intervention adherence, and attrition rate.

Acceptability

时间窗: 12 weeks post-allocation

A 5-item satisfaction survey will be conducted by the end of the intervention for participants to rate the intervention in terms of appropriates of the session content, length of each session, overall intervention duration and delivery mode, from 1 (very dissatisfied) to 5 (very satisfied).

次要结局

  • Frailty level(12 weeks post-allocation)
  • Depressive symptoms(12 weeks post-allocation)
  • Quality of life(12 weeks post-allocation)
  • Physical functioning(12 weeks post-allocation)
  • Instrumental activities of daily living(12 weeks post-allocation)
  • Social support(12 weeks post-allocation)
  • Activities of daily living(12 weeks post-allocation)
  • Subjective well-being(12 weeks post-allocation)

研究者

发起方
TAO An
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

TAO An

Mr

Chinese University of Hong Kong

研究点 (1)

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