Viewing Study NCT07365020


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Study NCT ID: NCT07365020
Status: COMPLETED
Last Update Posted: 2026-01-23
First Post: 2026-01-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Feasibility RCT of Culturally Appropriate Physical Activity Strategies for Older Chinese Adults in the UK
Sponsor: University of Manchester
Organization:

Study Overview

Official Title: A Feasibility Randomised Controlled Trial of Culturally Appropriate Physical Activity Promotion Strategies Among Older Chinese Adults in the UK
Status: COMPLETED
Status Verified Date: 2026-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: