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Pilot Project on Enhancing Support for Hidden Elderly in the Three-nil Buildings and Old Tenement Buildings: Capacity Building & Impact Evaluation

2026年11月1日 更新者:Prof. Yu, Doris Sau Fung、The University of Hong Kong

The aims of this interventional study are of two-fold. First, the study aims to develop the capacity to facilitate the collaborating NGOs to address the social determinants of aging well for 3-N seniors. The second aim of the study is to evaluate the impact of the transitional support for 3-N elders. The main question is aims to answer is:

Does the transitional support facilitate a better physical and psychological wellbeing in 3-N seniors.

Participants will be categorized into transitional-support group or non-transitional-support group based on their existing community service. They will join evaluation at four timepoints (baseline 3-, 6-, and 12-month) over the 1-year follow-up period.

研究概览

详细说明

The project will set up the following digital platform:

  1. Neighbor Link for Healthy Living
  2. Healthy Lifestyle Hubs without Walls
  3. Service Connect Compass Central to the concept of prompting 'aging well' through addressing the social determinants of health, the evaluation not only focuses on the direct impact on the social cohesion of the beneficiaries with their immediate community context, but also captures the indirect impact on the broader dimensions reflecting 'aging well'.

研究类型

介入性

注册 (估计的)

1520

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Doris Sau Fung YU, PhD
  • 电话号码:852-3917-6319
  • 邮箱:dyu1@hku.hk

学习地点

      • Hong Kong、香港
        • The University of Hong Kong
        • 接触:
          • Doris Sau Fung YU, PhD
          • 电话号码:852-3917-6319
          • 邮箱:dyu1@hku.hk

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Engaged in the transitional care model
  • Consent to participate in the impact evaluation
  • Able to complete the impact evaluation

Exclusion Criteria:

  • Unable or unwilling to provide informed consent
  • An acute or unstable health condition makes participation unsafe
  • Unable to complete research assessments despite reasonable support

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention status

This arm covers two major service dimensions including living support and district-based caring buddy network. Participants will join evaluation at four timepoints (i.e., baseline, 3-month, 6-month, 12-month)

Intervention will be conducted to improve lifestyle based on their needs which include 1) Neighbor Link for Healthy Living, 2) Healthy Lifestyle Hubs without Walls and 3) Service Connect Compass.

无干预:No-intervention status

The corresponding no-treatment status is defined as subjects who have not received any mapped intervention for the corresponding length of time.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Edmonton Frailty Scale
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Overall frailty

Changes from baseline to 3 month, 6 month, 12 month post-intervention.

次要结果测量

结果测量
措施说明
大体时间
Neighborhood Cohesion Inventory (HK version)
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Neighborhood cohesion and social engagement

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Life Space Assessment
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Life space mobility

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
3-item UCA Loneliness Scale
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Loneliness

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Health-Promoting Lifestyle Profile II
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Lifestyle behaviors

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Social Frailty Scale-8 items (SFS-8)
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Social vulnerability

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Short Physical Performance Battery
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Measuring by (range from 0 to 12), with higher score indicating better physical performance

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Geriatric Depression Scale
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Psychological wellness

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Mini-nutritional Assessment
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Vitality

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
5-minute Montreal Cognitive Assessment (MoCA)
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Measuring Cognitive function (range from 0 to 30), A score of 26 or over is considered to be normal.

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
EuroQoL-5 Dimension-5 Level
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Measuring Health-related quality of life (HRQL) (range from -0.59 to 1.0), higher score indicates better quality of life

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Insomnia Severity Index (ISI)
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Severity of sleeping problem

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Hearing Handicap Inventory
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

Hearing loss

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Handgrip
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

physical wellness

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
7-item Abbreviation Memory Inventory for the Chinese
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

subjective memory complaints

Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Body composition
大体时间:Changes from baseline to 3 month, 6 month, 12 month post-intervention.

the percentages of fat and muscle in the human body

Changes from baseline to 3 month, 6 month, 12 month post-intervention.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Doris Sau Fung YU, PhD、The University of Hong Kong

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年12月1日

初级完成 (估计的)

2030年12月1日

研究完成 (估计的)

2031年6月1日

研究注册日期

首次提交

2026年11月1日

首先提交符合 QC 标准的

2026年11月1日

首次发布 (实际的)

2026年11月5日

研究记录更新

最后更新发布 (实际的)

2026年11月5日

上次提交的符合 QC 标准的更新

2026年11月1日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • 3NIL

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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