An interventional study of Mapped intervention based on health status in 3-nil Buildings Seniors, sponsored by The University of Hong Kong. Not yet recruiting at 1 site in Hong Kong. Per ClinicalTrials.gov, last updated 2026-11-05.
Sponsored by The University of Hong Kong · Not applicable, Interventional, and Prevention
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.
The project will set up the following digital platform:
The University of Hong Kong is the lead sponsor of 1,292 studies on the registry; 348 are open to participants now.
Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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)
Behavioral: Mapped intervention based on health status
The corresponding no-treatment status is defined as subjects who have not received any mapped intervention for the corresponding length of time.
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.
Edmonton Frailty Scale
Overall frailty
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Neighborhood Cohesion Inventory (HK version)
Neighborhood cohesion and social engagement
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Life Space Assessment
Life space mobility
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
3-item UCA Loneliness Scale
Loneliness
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Health-Promoting Lifestyle Profile II
Lifestyle behaviors
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Social Frailty Scale-8 items (SFS-8)
Social vulnerability
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Short Physical Performance Battery
Measuring by (range from 0 to 12), with higher score indicating better physical performance
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Geriatric Depression Scale
Psychological wellness
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Mini-nutritional Assessment
Vitality
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
5-minute Montreal Cognitive Assessment (MoCA)
Measuring Cognitive function (range from 0 to 30), A score of 26 or over is considered to be normal.
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
EuroQoL-5 Dimension-5 Level
Measuring Health-related quality of life (HRQL) (range from -0.59 to 1.0), higher score indicates better quality of life
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Insomnia Severity Index (ISI)
Severity of sleeping problem
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Hearing Handicap Inventory
Hearing loss
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Handgrip
physical wellness
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
7-item Abbreviation Memory Inventory for the Chinese
subjective memory complaints
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Body composition
the percentages of fat and muscle in the human body
Time frame: Changes from baseline to 3 month, 6 month, 12 month post-intervention.
Plan to share: No
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.
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