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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07365020
Enrollment
30
Registered
2026-01-23
Start date
2024-09-01
Completion date
2025-09-01
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ethnic Minority Group, Physical Inactivity

Keywords

physical activity, ethnic minority group, intervention, randomised control trial, older Chinese adults, UK, Feasibility

Brief summary

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.

Interventions

BEHAVIORALThe culturally appropriate PA promotion strategies

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.

BEHAVIORALWHO leaflet group (control)

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.

Sponsors

University of Manchester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants are randomly assigned to either a culturally appropriate physical activity promotion strategies group or a control group receiving standard WHO physical activity information and are followed in parallel.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rateBaselineWe 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.
Compliance rate and follow-up rate.18 weeksParticipants 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.
Adherence12 weekIn this study, adherence was mainly assessed by the number of workshops attended by the participants.
Acceptability12 to 18 weekQualitative 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

MeasureTime frameDescription
Subjective measures of physical activityBaseline, 12-week and 18-weekSubjective measurement was conducted using the Chinese version of the Physical Activity Scale for the Elderly (PASE).
Objective measures of physical activitybaseline, 12-week and 18-weekA 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).
COM-B questionnairesBaseline, 12-week and 18-weekBrief COM-B questionnaires was used to assess the perceived capability, opportunity and motivation for PA behaviour among older Chinese adults in the UK.
Physical FunctionBaseline, 12-week and 18-weekThe Short Physical Performance Battery (SPPB) will be used to assess the potential change of physical function
Health-related quality of lifeBaseline, 12-week and 18-weekThe CASP-12 (Control, Autonomy, Self-realisation, and Pleasure-12) questionnaire was used to measure older adults' health-related quality of life
Adverse eventsWhole study period-18 weeksA safety reporting protocol was followed for managing related and unexpected serious adverse events (SAEs) and directly attributable adverse events (AEs).

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026