- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07305441
Impact Assessment of the Jockey Club REACH & Map Program for Hard-to-reach Older Adults
Impact Assessment of the Jockey Club REACH & Map Program for Hard-to-reach Older Adults in the Community: A Target Trial Emulation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The overall aim of this project is to conduct a comprehensive impact assessment of the Jockey Club (JC) Reach & Map Program, utilizing a framework based on the World Health Organization (WHO) Health Impact Assessment. The study will evaluate how the program influences health outcomes among hard-to-reach older adults by assessing changes in key health determinants. The findings will be disseminated to relevant stakeholders to inform future policy setting and service planning, and long-term monitoring will be undertaken to evaluate the extent to which the impact assessment influences decision-making in aged care service development.
The primary focus of the evaluation is on the functional abilities of older adults, including physical, cognitive, psychological, and social functioning. The assessment will also cover core outcomes such as quality of life, frailty, and health service use, alongside person-centered measures like loneliness and mental health. Given the diverse services received by beneficiaries, the study will account for structural and social health determinants-such as age, gender, socio-economic status, and chronic disease burden-as covariates in the analysis. In addition, the project will explore the broader effects of the JC Reach & Map Program on aged care service utilization and document both the experiences of service recipients and stakeholders involved.
Specifically, the study objectives are: (1) to evaluate the impact of the JC Reach & Map Program on frailty, quality of life, and health service use among hard-to-reach older adults, focusing on physical, cognitive, psychological, and social functions; (2) to explore the engagement experiences and perceptions of older adults regarding the services received, and their impact on well-being, community engagement, and social integration; and (3) to explore the experiences of service stakeholders in reaching and working with this population, as well as to gather their insights on ideal service models and policies for hard-to-reach older adults.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Doris Sau Fung YU, PhD
- Phone Number: 852-3917-6319
- Email: dyu1@hku.hk
Study Locations
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-
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Hong Kong, Hong Kong
- Recruiting
- The University of Hong Kong
-
Contact:
- Doris Sau Fung Prof. Yu,
- Phone Number: +852 39176319
- Email: dyu1@hku.hk
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Principal Investigator:
- Doris Sau Fung Prof. Yu,
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age > 60
- able to participate in the impact assessment as evidence by a test score of > 6 on the Abbreviated Mental Test
- has the functional ability to engage in the digital intervention
- able to communicate with the researcher
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment status
To account for time bias, each subject will be created with two clones at time zero and assigned each of the two clones to either treatment or no-treatment status, respectively.
The treatment status in each evaluative endpoint (i.e., 1-month, 4-month, 10-month, and 13-month) is defined as subjects who have received the mapped intervention for the respective length of time since the time zero during which the intervention has just commenced.
|
Intervention will be conducted to improve lifestyle based on their needs which include 1) Home modification, 2) Lifestyle-based health promotion, 3) Geriatric symptom management, 4) Health counseling for chronic disease management, 5) Counseling-based service, 6) Social network optimization, 7) Social support optimization
|
|
No Intervention: No-treatment status
To account for immortal time bias, each subject will be created with two clones at time zero and assigned each of the two clones to either treatment or no-treatment status, respectively.
The corresponding no-treatment status is defined as subjects who have not received any mapped intervention for the corresponding length of time.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
EuroQoL-5 Dimension-5 Level
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
Measuring Health-related quality of life (HRQL) (range from -0.59 to 1.0), higher score indicates better quality of life
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Short Physical Performance Battery
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Measuring by (range from 0 to 12), with higher score indicating better physical performance
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
|
5-minute Montreal Cognitive Assessment (MoCA)
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Measuring Cognitive function (range from 0 to 30), A score of 26 or over is considered to be normal.
|
Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
|
7-item Memory Complaint Scale (MCS)
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
Measuring Subjective Memory Score (range from 0 to 14), lower score indicates better memory performance.
No MCs (0-2), Mild MCs (3-6), Moderate MCs (7-10), Severe MCs (11-14).
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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3-item University of California, Los Angeles (UCLA) Loneliness Scale
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Measuring Loneliness (range 3-9), higher score indicates greater loneliness.
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
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The 8-item Geriatric Depression Scale
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Measuring Depression (range 0 to 8), with higher score indicating higher risk of depression
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
|
|
8-item Social Connectedness Scale Revised
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Measuring Social connectedness (range 0 to 48), <22 indicates lack of social connectedness
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health service utilization
Time Frame: Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Self-developed checklist on community care service for older adults in Hong Kong
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Changes from baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Health service utilization
Time Frame: From baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Self-developed checklist on health service utilization (including visit to out-patient clinic, emergency medical service, an in-hospital service in private and/or public sectors). [generic] With the consent from the participants, the above information will be retrieved from the electronic health record. Otherwise, self-report method will be used for collecting the data. |
From baseline to 1 month, 4 month, 10 month, and 13 month post-intervention.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Doris Sau Fung YU, The University of Hong Kong
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- REACH & MAP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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