Skip to main content
OpenTrials
Completed

NCT Number: NCT07365020

Feasibility RCT of Culturally Appropriate Physical Activity Strategies for Older Chinese Adults in the UK

The goal of this study was to explore the feasibility and acceptability of conducting a feasibility randomised controlled trial of culturally appropriate physical activity (PA) promotion strategies among older Chinese adults living in the UK.

The main questions the study aimed to answer were:

Whether older Chinese adults in the UK were willing to take part in the study and to be randomly assigned to a group

Whether participants were willing to remain in the study for its full duration

Whether participants were willing to engage with the PA promotion strategies, including attending workshops, using a logbook, wearing a pedometer, and joining a social media support group

Whether participants found the PA promotion strategies and outcome measures acceptable

Whether physical activity, physical function, and quality of life showed changes in the intervention and control groups

Researchers compared the culturally appropriate PA promotion strategies with a World Health Organization (WHO) PA recommendation leaflet. The study lasted 18 weeks, including a 12-week intervention and a 6-week follow-up.

Participants in the intervention group received culturally appropriate PA promotion materials, including booklets, workshops, a social media support group, a resistance band for strength and balance exercises, and a pedometer.

Participants in the control group received a WHO PA information leaflet and a pedometer.

Participants in both groups completed data collection at three time points. At each time point, participants were asked to wear a pedometer for 7 days.

Completed

Looking for future studies?

Notify Me

Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The university of Manchester

Manchester, Great Manchester, M13 9PL, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 60 years or above;
  • Self-identified as Chinese ethnicity;
  • Speaking either Cantonese, Mandarin and/or English;
  • Able to read and write Chinese or English;
  • No time requirement for their stay in the UK, but they should have settled in the UK as residents and not as tourists.
  • Self-report not meeting the PA guidelines for older adults (engaging in less than 150 minutes of moderate-level PA each week and performing balance, strength, and flexibility exercises less than twice a week);
  • Self-report being able to walk around at home independently;
  • Can provide informed consent.

Exclusion criteria

  • Those who self-report that they already meet the PA guidelines (engaging in more than 150 minutes of moderate-level PA each week and performing balance, strength, and flexibility exercises more than twice a week), as this study focuses on older Chinese adults with insufficient PA.
  • Those who plan to be away from Manchester for more than 2 months during the intervention period.
  • Participants with diseases where exercise is contraindicated will be excluded to ensure the safety of the participants. A self-reported approach will be used to identify these conditions, including cognitive impairment, as it is considered more acceptable by PCIE participants than formal assessments such as the MMSE (Mini-Mental State Examination), which were viewed as burdensome. To mitigate potential bias, the research team will monitor participants throughout the study. Participants who show signs of impairment after giving consent, such as difficulty completing data collection or following instructions, will be excluded.

Treatment and study plan

The culturally appropriate PA promotion strategies

Behavioral

The intervention was developed based on the Behaviour Change Wheel, aiming to increase participants' capability, opportunity, and motivation to engage in physical activity. It consisted of three components: printed materials, group workshops, and an online social media support group.

  • The printed materials included three parts: a culturally appropriate core booklet; the Chinese version of the Otago home exercise booklet, and a physical activity logbook.
  • Participants were invited to attend three workshops over a 12-week period, scheduled every four weeks. The workshops were designed to reinforce the content of the booklets and included presentations, group exercises, and group discussions.
  • Participants were also invited to join a study-specific social media support group via WeChat or WhatsApp, depending on their preference. These groups provided peer support, opportunities to share physical activity goals and progress, and motivational messages and reminders from the researcher.

WHO leaflet group (control)

Behavioral

In the control group, participants received a printed leaflet outlining World Health Organization (WHO) physical activity recommendations for older adults. Participants were encouraged to follow these guidelines, including 150-300 minutes of moderate-intensity or 75-150 minutes of vigorous-intensity aerobic activity per week, along with strength and balance exercises twice weekly, at a time and place convenient to them. No additional support was provided.

Primary outcomes

  1. Recruitment rate

    Time frame: Baseline

    We aimed to recruit at least 30 participants within eight weeks. Detailed records were kept of the total number of potential participants approached by the researcher, the number of participants who attend the screening, and the number of participants who are ultimately included in the study.

  2. Compliance rate and follow-up rate.

    Time frame: 18 weeks

    Participants were not fully withdrawn from the study solely due to discontinuation of or noncompliance with the intervention. For example, participants could choose to stop attending workshops or participating in the social media group while still remaining willing to complete data collection activities. Alternatively, participation could be discontinued based on clinical judgment. Every effort was made to collect as much data as possible to maintain the integrity of the study. Reasons for participants' exit from the trial were recorded separately.

  3. Adherence

    Time frame: 12 week

    In this study, adherence was mainly assessed by the number of workshops attended by the participants.

  4. Acceptability

    Time frame: 12 to 18 week

    Qualitative interviews. At the end of the study, about 50% of participants (including those who withdraw from the trial) was invited for follow-up interviews.

Secondary outcomes

  1. Subjective measures of physical activity

    Time frame: Baseline, 12-week and 18-week

    Subjective measurement was conducted using the Chinese version of the Physical Activity Scale for the Elderly (PASE).

  2. Objective measures of physical activity

    Time frame: baseline, 12-week and 18-week

    A pedometer (Realalt 3DTriSport 3D Pedometer; 3DTriSport Pedometer for Walking with Clip and Lanyard - Realalt) was used to monitor participants' PA level (i.e., step counts).

  3. COM-B questionnaires

    Time frame: Baseline, 12-week and 18-week

    Brief COM-B questionnaires was used to assess the perceived capability, opportunity and motivation for PA behaviour among older Chinese adults in the UK.

  4. Physical Function

    Time frame: Baseline, 12-week and 18-week

    The Short Physical Performance Battery (SPPB) will be used to assess the potential change of physical function

  5. Health-related quality of life

    Time frame: Baseline, 12-week and 18-week

    The CASP-12 (Control, Autonomy, Self-realisation, and Pleasure-12) questionnaire was used to measure older adults' health-related quality of life

  6. Adverse events

    Time frame: Whole study period-18 weeks

    A safety reporting protocol was followed for managing related and unexpected serious adverse events (SAEs) and directly attributable adverse events (AEs).

Sponsors and collaborators

Lead sponsor

University of Manchester

Other

Registry information

Official study title

A Feasibility Randomised Controlled Trial of Culturally Appropriate Physical Activity Promotion Strategies Among Older Chinese Adults in the UK

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 23, 2026
Registry last updated
Jan 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.