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Recruiting NCT06450288

Effectiveness of GO for Transitional Housing Residents

No phase Interventional Quality of Life Wellness, Psychological

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: GO.
Who it may be relevant to
Registry conditions: Quality of Life, Wellness, Psychological. Basic parameters: from 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Hong Kong
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effectiveness of the Green Oasis (GO) Wellness Program for Residents Living in Concordia Tsat Sing Kong Transitional Housing Estate

Overview

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: 1. Increase health awareness and engaging in health promoting activities, including more physical activities/walking, gardening. 2. Enhance happiness and quality of life. Participants will: * complete physical exercises, gardening, and interact with the GO website * receive health talks

Interventions

  • Behavioral GO
    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.

Primary outcome measures

  • Quality of life (World Health Organization) [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
  • Happiness [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
  • Activities of daily living [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
  • Physical activity [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
  • Satisfaction with migration life [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
  • Pain intensity [Time frame: T0 (baseline), T1 (6 months), T2 (12 months)]
Secondary outcome measures (2)
  • Website evaluation [Time frame: 2 weeks after T2 (post-test)]
  • Semi-structured interview [Time frame: within 2 weeks after T2 (post-test)]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Prevention

Study locations

Hong Kong · 1 center
  • Hong Kong Metropolitan University — Hong Kong

Identifiers

NCT: NCT06450288 · GO

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗