- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06450288
Effectiveness of GO for Transitional Housing Residents
Effectiveness of the Green Oasis (GO) Wellness Program for Residents Living in Concordia Tsat Sing Kong Transitional Housing Estate
The goal of this pre-post study is to enhance the health and wellness of the residents in the Concordia Tsat Sing Kong Transitional Housing Estate. This study aims to evaluate the effectiveness of the Green Oasis (GO) wellness program in:
- Increase health awareness and engaging in health promoting activities, including more physical activities/walking, gardening.
- Enhance happiness and quality of life.
Participants will:
- complete physical exercises, gardening, and interact with the GO website
- receive health talks
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mimi Mun Yee Tse, PhD
- Phone Number: 39708764
- Email: mmytse@hkmu.edu.hk
Study Locations
-
-
-
Hong Kong, Hong Kong
- Recruiting
- Hong Kong Metropolitan University
-
Contact:
- Mimi Mun Yee Tse, PhD
- Phone Number: (852)39708764
- Email: mmytse@hkmu.edu.hk
-
Sub-Investigator:
- Denis Siu On Chan, MSc
-
Sub-Investigator:
- Tyrone Tai On Kwok, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 10 or above.
- Scored >6 in the Abbreviated Mental Test; a cut-off point of 6 is valid in differentiating between normal and abnormal cognitive functions for geriatric clients.
- Can understand Cantonese.
- Able to take part in light exercise and stretching.
- Have access to smartphone and internet.
Exclusion Criteria:
- Have a serious organic disease or malignant tumor.
- Have a mental disorder diagnosed by neurologists or psychiatrists.
- Experienced drug addiction
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GO group
Participants who reside in the Concordia Tsat Sing Kong Transitional Housing Estate (still under construction) will be invited to join the GO wellness program.
|
Green Oasis wellness program: include physical exercises, gardening, interaction with the developed website. Participants' general health status and website evaluation will be measured at T0 (baseline), T1 (3 months), T2 (9 months), using standardized questionnaires. Study Design: pre-post study, 50 participants will be recruited from the Concordia Tsat Sing Kong transitional housing estate. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life (World Health Organization)
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Conducting pre- and post-test of WHOQOL-BREF.
The brief, Chinese version of the World Health Organization's quality of life scale (WHOQOL-BREF) has our domains: physical health, psychological health, social relationships, and environment.
A 5-point response scale is used in the scale.
Higher scores indicate higher quality of life.
WHOQOL-BREF has good validity and reliability.
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
|
Happiness
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Conducting pre- and post-test of Subjective Happiness Scale (SHS).
The Subjective Happiness Scale's Chinese adaptation (SHS) consists of 4 items to measure individual levels of subjective happiness.
It features 4 questions, each evaluated on a 7-point Likert scale, where a higher score signifies a higher degree of subjective happiness
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
|
Activities of daily living
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Conducting pre- and post-test of Activities of Daily Living Questionnaire (ADLQ).
The activities of daily living questionnaire (ADLQ) will be measured by the Barthel Index, which consists of 10 items of ADL, including mobility and self-care ability.
It refers to the basic self-care tasks that individuals perform daily to maintain their overall well-being and take care of themselves; the activities include eating, grooming, bathing, and dressing.
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
|
Physical activity
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Conducting pre- and post-test of the 5-Item Physical Activity Questionnaire.
The Chinese adoption of the 5-item physical activity questionnaire will be used to assess the physical activity levels of the participants.
This questionnaire uses a 5-point Likert scale to assess five items: frequency, duration, intensity, overall length, and type of activities the participants perform during their spare times.
The test-retest reliability of this questionnaire is between 0.61 and 0.91, indicating its usefulness.
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
|
Satisfaction with migration life
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Conducting pre- and post-test of the Satisfaction With Migration Life Scale (SWMLS).
The Chinese adoption of the Satisfaction With Migration Life Scale (SWMLS) to assess participants' satisfaction with their life after moving in to transitional housing.
The scale has 5 questions in total and follows a 7-point Likert scale, with some modifications on the wordings according to the study.
SWMLS has good validity and reliability.
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
|
Pain intensity
Time Frame: T0 (baseline), T1 (6 months), T2 (12 months)
|
Pain will be measured using the Chinese version of the Brief Pain Inventory to assess the multidimensional nature of the participants' pain, including intensity and interference with daily activities over the past 24 hours.
The total scores for pain severity (four items) range from 0 to 10, with higher scores indicating more severe pain.
This scale demonstrated good reliability, with coefficient alphas greater than 0.70
|
T0 (baseline), T1 (6 months), T2 (12 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Semi-structured interview
Time Frame: within 2 weeks after T2 (post-test)
|
Interview participants about joining the program, their perceived benefits, challenges, etc.
|
within 2 weeks after T2 (post-test)
|
|
Website evaluation
Time Frame: 2 weeks after T2 (post-test)
|
Website will be assessed using the Chinese version of the System Usability Scale (SUS).
The SUS consists of 10 items rated using a 5-point Likert scale.
A higher total score indicates better quality of the rated system.
This scale has good reliability, with a Cronbach's alpha of 0.84.
|
2 weeks after T2 (post-test)
|
Collaborators and Investigators
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO
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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