Skip to content

Pilot Feasibility Study of a Fall Prevention Exercise Programme for Community-dwelling Older Adults in Nanchang, China

Pilot Feasibility Study of a Fall Prevention Exercise Programme for Community-dwelling Older Adults in Nanchang, China

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07341802
Enrollment
36
Registered
2026-01-14
Start date
2026-03-16
Completion date
2027-01-30
Last updated
2026-04-29

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

Conditions

Fall Prevention

Keywords

Fall prevention, Exercise adherence, Older adults

Brief summary

The goal of this pilot clinical trial is to evaluate the feasibility of a fall prevention exercise programme for older adults living in urban communities in China. The study will also gather preliminary data on whether the programme can improve adherence to exercise and reduce falls. The main questions it aims to answer are: * Is the Safe & Joyful Walk programme feasible and acceptable for older adults in urban China? * Does the programme help participants stick to regular exercise? * Does the programme show early signs of improving balance, walking speed, and reducing falls? Researchers will compare the Safe & Joyful Walk programme to Tai Chi to see which approach may better support exercise adherence and fall prevention. Participants will: * Attend 24 instructor-led group exercise sessions over 12 weeks * Complete additional unsupervised home-based exercise practices during the same 12-week intervention period * Continue unsupervised exercises during a 24-week follow-up period to assess long-term adherence * Complete surveys, interviews, and physical tests at baseline, 12 weeks, and 36 weeks * Record their exercise and any falls in diaries and calendars

Interventions

BEHAVIORALSafe & Joyful Walk

A 12-week group-based exercise programme designed to improve balance, strength, and functional mobility. Participants attend 24 instructor-led sessions and complete additional home-based practices, with the combined duration of group and home sessions reaching the target of 120 minutes of exercise per week. Instructional videos, printed manuals, and WeChat reminders support adherence.

BEHAVIORALTai Chi

A 12-week group-based Tai Chi programme using the simplified 24-form Yang-style routine. Participants attend 24 instructor-led sessions and complete additional home-based practices, with the combined duration of group and home sessions reaching the target of 120 minutes of exercise per week. Instructional videos, printed manuals, and WeChat reminders support adherence.

Sponsors

University of Malaya
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

In addition to outcomes assessors, the data analysts are masked to group allocation. The dataset provided for analysis uses coded group labels ("Group A" and "Group B"), and the analysts remain blinded until after the primary analyses are complete.

Eligibility

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

Inclusion criteria

* age 60 years or older; * Mandarin-speaking; * independent in activities of daily living; * able to walk 10 m without the use of a walking aid; * willingness to provide informed consent and comply with the study protocol.

Exclusion criteria

* an acute psychiatric condition with psychosis; * an unstable medical condition that would preclude safe participation; * a progressive neurological condition (such as Parkinson's disease, multiple sclerosis, Meniere's disease); * cognitive impairment defined as a Pfeiffer Short Portable Mental Status Questionnaire (SPMSQ) score \<8 ; * residing in residential aged care, currently participating in a fall prevention trial.

Design outcomes

Primary

MeasureTime frameDescription
Safety of the intervention (adverse events)Baseline to 36 weeks.Safety will be assessed by the number and type of adverse events reported by participants and recorded in exercise diaries throughout the 12-week programme and 24-week follow-up.
Recruitment rateUp to 4 weeksRecruitment will be assessed by the proportion of eligible participants enrolled, recorded in the Study Screening Log.
Attrition rateBaseline to 36 weeksAttrition will be assessed by the proportion of participants who withdraw before completing the 36-week follow-up, recorded in the Withdrawal Log.
Fall rateBaseline to 36 weeksFalls will be tracked using participant fall calendars with monthly telephone verification; outcomes include number of falls and fallers over the 36-week period.

Secondary

MeasureTime frameDescription
Attendance at group sessionsBaseline to 12 weeksAttendance will be assessed by the number and proportion of sessions attended, recorded in Attendance Logs.
Adherence to home-based practiceBaseline to 36 weeksAdherence will be assessed using Exercise Diaries, documenting frequency and duration of home-based practice.
Balance confidence (Activity-specific Balance Confidence Scale, ABC)Baseline, 12 weeks and 36 weksBalance confidence will be assessed using the Activity-specific Balance Confidence (ABC) Scale, a 16-item self-report questionnaire measuring confidence in performing daily activities without losing balance. Scores range from 0% to 100%, with higher scores indicating greater balance confidence.
Gait speed (4-meter gait speed test)Baseline, 12 weeks and 36 weeks.Usual gait speed will be measured over 4 meters using standardized procedures; faster speed indicates better performance.
Balance performance (One-Leg Stance test)Baseline, 12 weeks and 36 weeks.Static balance will be assessed using the One-Leg Stance test; longer stance time indicates better balance.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026