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CompletedNCT06202482Updated Sep 19, 2024

Enhance Physical Activity and Intergenerational Relationship Via Connect Active Program (CAP): a Pilot Randomized Controlled Trial

An interventional study of Connect Active Program in Elderly and Physical Inactivity, sponsored by The Hong Kong Polytechnic University. Completed at 1 site in Hong Kong. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by The Hong Kong Polytechnic University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study investigates how walking exercises and technology could enhance the quality of life in the older generation. It has three objectives: 1) To examine the effectiveness of the Connect Active Program (CAP) in improving intergenerational relationships, psychological well-being, and physical fitness for older adults; 2) To teach older adults to use mobile apps; 3) To examine the experiences and feedback from participants in using the apps and joining the CAP. This research will provide long-term insights into improving the overall health outcomes of older adults via intergenerational support and increasing the acceptance of mobile technology among older adults.

02

Conditions studied

  • Elderly
  • Physical Inactivity

Keywords

  • Connective Active Program
03

In context

Lead sponsor

The Hong Kong Polytechnic University is the lead sponsor of 659 studies on the registry; 250 are open to participants now.

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

04

Who can participate

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

Inclusion criteria

  • Younger Adults/Participants:

    • Aged 18 to 30
    • Related to the older adult participant (i.e. family member, relatives)
    • Able to understand Cantonese
    • Own a smartphone and have access to the Internet
    • Able to take part in walking exercise and stretching program
  • Older Adults/Participants:

    • Aged 60 or above
    • Able to understand Cantonese
    • Own a smartphone and have access to the Internet
    • Capable to participate in walking exercise and stretching program

Exclusion criteria

Exclusion Criteria:

  • Older Adults/Participants and Younger Adults/Participants:

    • Diagnosed with a mental disorder by neurologists or psychiatrists
    • With a history of drug addiction
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    Experimental group

    Participants in the intervention group will participate in a 6-week Connect Active Program (CAP). Young participants will be the pioneers and take the initiative to change their inactive and sedentary lifestyles by including exercise into their daily routines about once a week, at least 45 minutes each time. For instance, they could organize family field trips to waterfront parks or involve their older family members in their favorite sports. All walking activities included in the study should be done with the Nike Run Club App for record and outcome measures. For other activities in CAP, participants will use other apps following that week's topic. For instance, they will use Google Maps to search for the best routes to their destinations; transportation apps such as Kowloon Motor Bus, Long Win Bus, and Mass Transit Railway apps to search for stops and exits.

    Other: Connect Active Program

  • No intervention
    Control group

    Participants in the control group will be provided with a leaflet as usual care. The pamphlet contains information about the benefits and some instructions for walking exercises for older adults.

Interventions

  • OtherConnect Active Program

    Younger adults will help older adults increase their digital literacy, skills, and desire to exercise and become more physically active via the proposed intervention. The Connect Active Program will consist of two components: walking exercises and mobile apps.

06

What researchers measure

Primary outcomes

  1. Aerobic Capacity and Endurance Evaluation with 6-Minute Walk Test (6MWT)

    It is initially created to assist in the examination of cardiopulmonary patients developed by the American Thoracic Society. It is a light-intensity exercise test to evaluate the aerobic capacity, endurance and oxygen saturation.

    Time frame: Baseline, Week 6

Secondary outcomes

  1. Mobility and Balance Assessment with Time Up and Go Test

    To assess mobility, movement, static balance and dynamic in people with musculoskeletal impairments, conditions related to aging, quality of life, and pain. The instructions are given as standing up from a chair, walking 3 meters, turning, and back to sit.

    Time frame: Baseline, Week 6

  2. Quality of Life Measurement

    Quality of life will be evaluated utilizing the World Health Organization Quality of Life-BREF (WHOQOL-BREF). It contains four realms: physical health, psychological health, social relationships, and environment. A 5-point response scale is used in the scale. WHOQOL-BREF has good validity and reliability.

    Time frame: Baseline, Week 6

  3. Happiness Level Determination

    A 29-item measure of happiness; from 1 "strongly agree," to 6, "strongly disagree." The scale's reliability was 0.91.

    Time frame: Baseline, Week 6

  4. Intergenerational Relationship Appraisal

    The intergenerational relationship quality scale (IRQS) to appraise the changes in intergenerational relationships, this questionnaire will allow the older participants to self-rate the relationship between the two generations. A 5-point response scale is applied in the scale.

    Time frame: Baseline, Week 6

  5. Subjective Quality Assessment of Mobile Apps

    The 4-item subjective quality subscale of the Mobile Application Rating Scale (MARS) will be deployed to assess the overall quality of mobile apps involved in this study. MARS incorporates four objective quality subscales (engagement, functionality, aesthetics, and information quality) and one subjective quality subscale. Since a lengthy questionnaire would be complicated for the older participants to complete, we will only adopt the subjective quality subscale. All four items are assessed on a 5-point scale. The subjective quality subscale showed excellent internal consistency (alpha = 0.93) and interrater reliability intraclass correlation coefficient (ICC = 0.83). Higher scores indicate a higher level of subjective quality.

    Time frame: Baseline, Week 6

  6. Participant Feedback Collection

    Semi-structured interview for older and younger participants: Individual interviews will be carried out by the Research Assistant upon completion of the CAP (post-test). They will be asked to comment on the perceived benefits, limitations and barriers in the program and the mobile apps, usefulness of the mobile apps, and recommendations for improving the CAP to meet their needs. Details of the questionnaire.

    Time frame: Baseline, Week 6

07

Study locations

1 site
  • Hong Kong Metropolitan University
    Kowloon, Hong Kong
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06202482
Lead sponsor
The Hong Kong Polytechnic University
Responsible party
TSE Mun Yee Mimi (Professor, The Hong Kong Polytechnic University) — Principal investigator
First posted
Jan 11, 2024
Start date
Jan 1, 2024
Primary completion
Mar 31, 2024
Completion
May 16, 2024
Last update
Sep 19, 2024

Study contacts

Mimi MY Tse, PhD
principal investigator · School of Nursing and Health Studies, Hong Kong Metropolitan University

Oversight

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

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