- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05207215
Study on the Steps to Avoid Falls in the Elderly (SAFETRIP)
Use of Video Consultation, Computer Gaming and Self-help Home Exercises as Steps to Avoid Falls in the Elderly
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Falls are the most common morbid and expensive health condition involving older adults. The range of exercises included in the SAFE programme is designed to be adaptable to a wide range of physical functions targeting pre-frail older adults. The exact exercises will vary on the patients' functional status. However, all exercise sessions must include balance exercises that challenge the patient's balance during static activities, during movement and also may include challenges as the patient has divided attention (walking and talking, walking while carrying objects). Balance is first emphasised followed by strengthening exercises of the lower extremities. The improvement in walking, physical activity and endurance, is dependent on the patients' improvement in balance and strength. The overall design of the intervention is to develop and maintain functional mobility by targeting deficiencies in balance, strength, mobility, and endurance.
Despite efforts to provide exercises to improve patients' balance and strength to prevent falls, many do not comply with the programme upon discharge. To address this challenge, the investigators propose to conduct a pilot study that will employ novel approaches, using an evidence-based, person-centred falls prevention intervention (SAFE programme), which is sustainable and cost-effective for the general public in Singapore. These three interventions in the study include video conferencing, newly created exercise games (Gamification) and a self-guided home exercise programme.
A key aspect of the SAFE exercise programme is its simple yet structured series of exercises, with gradual progression, to improve balance, mobility and lower limb strength. It is important that subjects continually challenge themselves during the exercise sessions to promote ongoing improvement in physical function. An exercise stratification grid has been developed to help guide the subjects on the types of exercises and level of intensity, that will be appropriate for them. Performance level (as defined in the stratification grid) should be re-assessed weekly so as to track the progress of the subject i.e. once a subject has achieved the level of the specified exercise in a category, the participants will progress to the next level for the same category. In addition, the subjects will be encouraged to participate in walking both, as much and as far as possible, to improve their functional capacity. Therefore, the SAFE exercises are very appropriate to be used in the home setting.
140 pre-frail subjects discharged from SKH, SGH and OCH will be recruited for the study. Only those who meet the requirements criteria using the Ward PT Checklist will be randomised into the 3 intervention groups. All groups are required to exercise at least twice a week and complete the intervention over a 3-month period. Baseline, 3- and 9-months follow-up data will be collected by independent assessors. Outcome measures in 9 categories will be measured and compared across the 3 groups. These measures will be correlated to the subject's compliance to the intervention and effectiveness will be compared between the 3 groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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State *
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Singapore, State *, Singapore, 169608
- Singapore General Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age >= 60 years
- Singapore citizen or Permanent Resident
- With or without fall history in the last one year
- Short Physical Performance Battery (SPPB) >= 6
- Ability to provide informed consent
- Has not more than 1 major comorbidity (Heart attack, heart failure, cerebrovascular disease & cancer)
- Abbreviated Mental Test (AMT) >= 6
- Not referred for further active rehabilitation with a physiotherapist after discharge from hospital or outpatient care.
Exclusion Criteria:
- Patients who are advised by their physicians not to participate in physical activity sessions will be excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A: Video Conferencing
Video conferencing is a 2-way interactive session that is enabled using telecommunication networks and the internet.
The investigators will be working with 3rd party provider to create the video conferencing platform.
Subjects can login to do SAFE exercises while physiotherapists monitor remotely.
Subjects will complete two sessions per week (1hour for each session) for 12 weeks.
|
The study developed 3 approaches that innovate beyond the existing delivery modes of the SAFE programme, by developing means for providing an intervention that is functionally equivalent to the SAFE programme but can be implemented in a patient's home.
These home approaches include: (a) video conferencing; (b) gamification; and (3) self-guided home exercise programme.
The investigators' task is to focus on developing these 3 modes and evaluating each in a pilot context for participants upon discharge from the hospital.
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Active Comparator: Group B: Gamification
Gamification refers to exercise-driven gaming, where games are developed with specifications/parameters that incorporate exercise movements.
Currently, the investigators have an ongoing pilot study on game-assisted rehabilitation at SGH Physiotherapy Outpatient clinic and the exercise games are developed by an external company.
The investigators will engage an external company to develop exercise games based on the exercises used in SAFE programme.
Each game will have different difficulty levels to provide progressive training for subjects
|
The study developed 3 approaches that innovate beyond the existing delivery modes of the SAFE programme, by developing means for providing an intervention that is functionally equivalent to the SAFE programme but can be implemented in a patient's home.
These home approaches include: (a) video conferencing; (b) gamification; and (3) self-guided home exercise programme.
The investigators' task is to focus on developing these 3 modes and evaluating each in a pilot context for participants upon discharge from the hospital.
|
|
Active Comparator: Group C: Self Guided
Subjects in the self-guided exercise programme will be instructed to do SAFE exercises at least twice a week for an hour each by themselves.
|
The study developed 3 approaches that innovate beyond the existing delivery modes of the SAFE programme, by developing means for providing an intervention that is functionally equivalent to the SAFE programme but can be implemented in a patient's home.
These home approaches include: (a) video conferencing; (b) gamification; and (3) self-guided home exercise programme.
The investigators' task is to focus on developing these 3 modes and evaluating each in a pilot context for participants upon discharge from the hospital.
|
|
Placebo Comparator: Group D: Self Guided
Subjects in the self-guided exercise programme will be instructed to do SAFE exercises at least twice a week for an hour each by themselves.
|
The study developed 3 approaches that innovate beyond the existing delivery modes of the SAFE programme, by developing means for providing an intervention that is functionally equivalent to the SAFE programme but can be implemented in a patient's home.
These home approaches include: (a) video conferencing; (b) gamification; and (3) self-guided home exercise programme.
The investigators' task is to focus on developing these 3 modes and evaluating each in a pilot context for participants upon discharge from the hospital.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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To monitor the change of SPBB over the study period
Time Frame: Baseline, 3rd month and 9th month
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The SPBB will be captured at 3 time points (1st during the baseline, 2nd during the 3rd month post assessment and 3rd during the 9 month post assessment).
Direct measurement will be taken by the assessor.
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Baseline, 3rd month and 9th month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Demographic Profile
Time Frame: Baseline, 3rd month and 9th month
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The following will be collected Age, gender, ethnicity, marital status via an interview
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Baseline, 3rd month and 9th month
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Profile of the Caregiver
Time Frame: Baseline, 3rd month and 9th month
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This profile will be collected via an Interview
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Baseline, 3rd month and 9th month
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Health Status: Presence of diseases
Time Frame: Baseline, 3rd month and 9th month
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This information will be collected via an interview
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Baseline, 3rd month and 9th month
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Health Status: Lawton IADL
Time Frame: Baseline, 3rd month and 9th month
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This information will be collected via an interview
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Baseline, 3rd month and 9th month
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History & Attitude Towards Falls
Time Frame: Baseline, 3rd month and 9th month
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This information will be collected via an interview
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Baseline, 3rd month and 9th month
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Social Network & Social Isolation
Time Frame: Baseline, 3rd month and 9th month
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Variables for Lubben Social Network Scale (LSNS-6) are collected via interview.
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Baseline, 3rd month and 9th month
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Healthcare Utilisation
Time Frame: Baseline, 3rd month and 9th month
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The following variables are collected via interview:
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Baseline, 3rd month and 9th month
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Quality of Life Characteristics
Time Frame: Baseline, 3rd month and 9th month
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Variables for EQ-5D-5L are collected via interview.
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Baseline, 3rd month and 9th month
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Compliance of the different Intervention
Time Frame: Baseline, 3rd month and 9th month
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Variables for compliance are being collected via log book and weekly calls.
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Baseline, 3rd month and 9th month
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Celia IC Tan, PhD, SingHealth Services
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SAFE TRIP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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