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CompletedNCT03918720Updated Dec 17, 2024

The Health and Effect of Health Empowerment Programmes Among Families in Tung Chung

An interventional study of Trekkers Family Health Empowerment Programme in Quality of Life and Empowerment, sponsored by The University of Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 6 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-17.

Sponsored by The University of Hong Kong · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 4 years 9 months after the study started (first participant enrolled Feb 2013, registered Nov 2017).
Phase
Not applicable
Study type
Interventional
Enrollment
1,200
Allocation
Non-randomized
Ages
6 Years and older
Sex
All
01

Study summary

Kerry Group Kuok Foundation Limited (KGKF) has initiated the Trekkers Family Project that aims to enable low-income families to develop their full potentials by providing support and opportunities in education, employment, environmental harmony and health. Health is an essential component to enable a person to develop his/her full potential. This study looks into one of the key elements, health, of members of low-income families and the effect of health education, health enablement and mutual health support on health and social outcomes. It is a cohort study of around 800 subjects from 200 families of the Trekkers Family Project, and around 800 subjects not included in the Trekkers Family Project in Hong Kong, recruited base on pre-defined inclusion criteria. Health empowerment interventions consisting of three inter-related programmes, namely, the Health Literacy, the Self-care Enablement, and the Health Ambassador Programmes.

Read the detailed description

The Health Literacy Programme aims to improve the knowledge on health and health services in order to promote health, prevent disease, and the proper use of services. It consists of four seminars per year on common health problems, mental health and cognitive health, etc.

The Self-Care Enablement Programme is to enable participants to keep themselves healthy, to build up self-efficacy and proper help-seeking skills, and to generate a spirit of mutual support among families. Two programmes will be delivered yearly, each with six 2.5 hour workshops facilitated by professional and lay leaders.

The Health Ambassador Programme aims to train up a group of adults recruited from the Trekkers families to act as a lay-advisor to other families on health issues. Participants who have completed the Health Literacy and Self-care Enablement programme will be given priority to take part in the Health Ambassador training programme.

The outcome measures are health enablement, health status, health-related quality of life, life style, cardiovascular risk factors, illnesses rates, and health service utilization pattern. All subjects in the cohort study will be surveyed on enrolment, and then yearly for 5 years. An age-gender appropriate health assessment will be carried out at baseline and at the end of five years for each subject. Changes in the outcomes will be evaluated and compared between groups. The impact of the health intervention programmes will be assessed.

02

Conditions studied

  • Quality of Life
  • Empowerment

Keywords

  • Quality of Life
  • Empowerment
  • Low-income Families
  • Parent-child health relationship
03

In context

Lead sponsor

The University of Hong Kong is the lead sponsor of 1,262 studies on the registry; 340 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Intervention group (inclusion criteria of Trekkers Families)

    1. Participants included must be part of a family whom all family members are usual residents in Tung Chung;
    2. The family must have at least one family member working full-time or part-time;
    3. The family household income does not exceed 75% of monthly median income of Hong Kong;
    4. At least one child studying Primary 1,2 or 3 at the time of recruitment; and
    5. At least one adult family member must be willing to participate in the long-term follow up study.
    6. Only fathers, mothers and children aged 6 or above will be included in this study.
  2. Control group

    1. Participants included must be part of a family whom all family members are usual residents in Hong Kong;
    2. The family household income does not exceed 75% of monthly median income of Hong Kong;
    3. At least one child studying Primary 1, 2 or 3 at the time of recruitment;
    4. Only fathers, mothers and children aged 6 or above will be included in this study.

Exclusion criteria

Exclusion Criteria:

  1. None of the family member was able to understand or communicate in Chinese language,
  2. The family is receiving Comprehensive Social Security Assistance (CSSA),
  3. Refuse to give consent.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,200 participants (actual)

Study arms

  • Experimental
    Trekkers

    Behavioral: Trekkers Family Health Empowerment Programme

  • No intervention
    Controls

Interventions

  • BehavioralTrekkers Family Health Empowerment Programme

    Health Assessment, Health Enablement and Health Literacy provided to empower participants awareness towards a healthier life style

    Also known as: Trekkers Family

06

What researchers measure

Primary outcomes

  1. Change from Patient enablement measured by the Chinese (HK) Patient Enablement Instrument at 60 months

    Patient Enablement Instrument-version 2 (PEI-2), score range 5 to 30, higher scores mean better enablement.

    Time frame: Up to 60 months

Secondary outcomes

  1. Change from Baseline Health Status (global health, mental health) measured by DASS at 60 month

    Depression, Anxiety and Stress Scales (DASS), three subscales, each with a score range of 0 to 42, higher scores mean more emotional problems.

    Time frame: Up to 60 months

  2. Change from Baseline Health-related quality of Life at 60 months

    12-item Short Form Health Survey-version 2 (SF-12v2) in adults: Physical Component Summary and Mental Component Summary scores, norm-based with a population mean of 50 and SD of 10, higher score means better quality of life. Child Health Questionnaire-Parent Form-28 items: Total Difficulty summary score ranges from 0-40, higher scores mean more behavioral difficulties; a prosocial scale score ranges from 0 to 10, higher scores mean better behavior.

    Time frame: Up to 60 months

  3. Change from Baseline Lifestyle to 60 months

    proportion of participants with unhealthy lifestyle including smoking, \<150min/wk of exercises, consumption of surgery drinks, smoking cigarettes, consumption of less than 5 portions of fruits and vegetables.

    Time frame: Up to 60 months

  4. Change from Baseline Health parameters to 60 months

    Cardiovascular Health Index (CVHI) measured by optimal blood pressure, body mass index, blood cholesterol, blood glucose, smoking status, physical activity, and fruit and vegetable intake, score ranges from 0 to 7, higher scores mean better CVH.

    Time frame: Up to 60 months

  5. Change from Baseline Health service utilization pattern to 60 months

    Proportion of people who reported to Have a family doctor, self-care for an illness, use of Accident and Emergency service during an illness episode.

    Time frame: Up to 60 months

Other outcomes

  1. Change from Baseline Health knowledge test to 60 months

    pre and post knowledge test after each health education course.

    Time frame: Up to 1 year

  2. Overall satisfaction after program

    Proportion of participants who reported overall satisfaction with the program.

    Time frame: Up to 1 year

07

Study locations

1 site
  • The University of Hong Kong
    Hong Kong, Hong Kong
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03918720
Lead sponsor
The University of Hong Kong
Responsible party
Professor Cindy L.K. Lam (Danny D B Ho Professor in Family Medicine and Department Head, The University of Hong Kong) — Principal investigator
First posted
Apr 17, 2019
Start date
Feb 1, 2013
Primary completion
Dec 31, 2022
Completion
Jun 30, 2023
Last update
Dec 17, 2024

Study contacts

Cindy Lo Kuen Lam
principal investigator · The University of Hong Kong

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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