Effects of an Individual and Family Self-Management of Fall Prevention Program on Balance Ability and Fall-related Self-efficacy Among Chinese Post-Stroke Individuals
1 other identifier
interventional
60
1 country
1
Brief Summary
This study is about exploring the effectiveness of individual and family self-management (IFSM) fall prevention programs on balance ability and fall-related self-efficacy in post-stroke people. The main intervention measures were developed based on the risk and protective factors of fall prevention in post-stroke people, including exercise, environment safety, assistant technology, medication review, and safety in daily activities. The intervention was implemented in 10 weeks for both patients and their family members. By mastering these skills, post-stroke people may reduce the number of falls after discharge to home.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 27, 2024
CompletedFirst Posted
Study publicly available on registry
August 29, 2024
CompletedStudy Start
First participant enrolled
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedJune 29, 2025
June 1, 2025
9 months
August 27, 2024
June 26, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
Fall-related self-efficacy
Fall-related self-efficacy refers to the level of perceived confidence in undertaking everyday activities without falling, which includes self-efficacy in balance ability, preventing falls, and managing falls. The Short Falls Efficacy Scale-International (Short FES-I) will be used to assess fall-related self-efficacy; it consists of seven questions. A four-point scale is used to score each item, and a higher score indicates lower self-efficacy. The total score is calculated by adding the scores of each item, giving a scale ranging from 7 to 28 for the seven items. The Short FES-I has previously demonstrated excellent reliability (Cronbach's α = 0.92).
Fall-related self-efficacy will be measured before the fall prevention program and after patients are discharged in 8 weeks.
Balance ability
Balance ability is the ability to maintain the body's stability, including keeping a certain posture or balance when subjected to external forces. Berg Balance Scale (BBS) will be used to assess the balance ability in post-stroke people. The BBS will be used to assess balance ability in post-stroke individuals. It consists of 14 items, each rated on a five-point scale. A score of 41-56 indicates the ability to walk independently, 21-40 indicates the ability to walk with assistance, and 0-20 indicates wheelchair-bound movement. In different studies on patients with stroke, the BBS has been found to have excellent internal consistency, with Cronbach alphas ranging from 0.92 to 0.98
Balance ability will be measured before the fall prevention program and after patients are discharged in 8 weeks.
Secondary Outcomes (1)
Number of falls, fall-related injuries and Adverse Events
Number of falls and fall-related injuries will be measured after patients are discharged in 8 weeks
Study Arms (2)
individual and family self-management (IFSM) fall prevention program
EXPERIMENTALThe IFSM program will be last for ten weeks, two weeks in the hospital, and follow up at eight weeks after patients discharge to home. It includes 11 sessions, including ten sessions developed in the inpatient department within two weeks and one online booster session developed in the first month (week 4) after discharge in home. There will be also one session just for caregivers, which aims to improve caregivers' skills to keep patients' safety. In the process, self-efficacy strategies, self-regulation skills, and social facilitation are used in every session. The main self-efficacy strategies includes skill mastery, vicarious experience, and verbal persuasion. Several self-regulation skills for patients and caregivers are also used in the study, such as self-monitoring and reflective thinking. A WeChat group will be established to support patients and their families.
usual care
NO INTERVENTIONParticipants in the control group will receive usual care, including standard clinical practices such as education on fall prevention and a fall prevention booklet. The education will be delivered by the researcher and does not include any additional intervention specific to the study. A fall prevention care plan will be manually documented in the electronic health record. After the patients are discharged home, a phone visit will be provided for patients within the first month, which will include a medication review and professional access. Participants will also use a fall record diary to record falls in the control group, and this will be copied for data extraction after the experiment.
Interventions
The IFSM program will last for ten weeks, two weeks in the hospital, and follow up at eight weeks after patients discharge to home. It will include 11 sessions, including ten sessions developed in the inpatient department within two weeks and one online booster session developed in the first month (week 4) after discharge in home. There will be also one session just for caregivers. Session 1 : PRST combined with GRI (one) Session 2 : Environment safety Session 3 : Assistant technology Session 4 : PRST combined with GRI (two) Session 5 : Medication review Session 6 : Safety in daily activities Session 7 : How to keep loved one safety Session 8 : Review of PRST combined with GRI Session 9 : Review of other five fall prevention skills Session 10 : Summary of the program and setting goals Session 11 : Booster session Week 10: Evaluation
Eligibility Criteria
You may qualify if:
- For patients
- aged 18 years or above;
- first-ever diagnosed with ischemic stroke;
- level of impairment assessed by the National Institutes of Health Stroke Scale (NIHSS) scores between 5 to 15 (moderate severity) before entering the experiment;
- mental state assessed by Mini-Mental State Exam score \> 24;
- mobility tested by Timed Up and Go ≥12.6 second (walkers or another kinds of gait aid are allowed to be used in the test);
- motor power of all limbs examined by muscle power assessment grade ≥3;
- ability to understand Chinese;
- living with family members;
- having phones that can use the internet;
- willing to join the study.
- For caregivers
- mental state assessed by Short Portable Mental Status Questionnaire score ≥8;
- being the primary caregiver, living in the same house, and taking care of the patient;
- having phones that can use the internet;
- +1 more criteria
You may not qualify if:
- having problems with sensory and/or global aphasia
- Discontinuation criteria:
- patients have an illness that needs hospitalization;
- patients and caregivers cannot complete participation in intervention sessions.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Affiliated hospital of Guizhou Medical University
Guiyang, Guizhou, 550004, China
Related Publications (1)
Wang Y, Chaiard J, Lirtmunlikaporn S, Suwankruhasn N. Effects of an individual and family self-management of fall prevention programme on balance ability and fall-related self-efficacy among Chinese poststroke individuals: a study protocol for a randomised controlled trial. BMJ Open. 2025 Jul 15;15(7):e100966. doi: 10.1136/bmjopen-2025-100966.
PMID: 40664404DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head nurse
Study Record Dates
First Submitted
August 27, 2024
First Posted
August 29, 2024
Study Start
October 1, 2024
Primary Completion
June 30, 2025
Study Completion
June 30, 2025
Last Updated
June 29, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- Individual participant data (de-identified) will be available upon reasonable request from the corresponding author. The data will be available beginning 6 months after publication for a period of 3 years. Data will be shared for academic purposes only.
- Access Criteria
- Access to the de-identified individual participant data (IPD) and supporting documentation (such as the study protocol, statistical analysis plan, and informed consent form) will be granted to qualified researchers affiliated with academic or non-profit institutions. Researchers must submit a methodologically sound research proposal along with a data access request to the corresponding author. The request will be reviewed by the study team to ensure alignment with the original study objectives and participant privacy protections. Upon approval, a data use agreement will be signed. Data will be shared via secure email or a secure file-sharing platform, depending on the nature and size of the data.
De-identified individual participant-level data related to the primary and secondary outcomes