- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05018455
The Effectiveness of Remote Fall Prevention Program vs. Face-to-Face
The Effectiveness of Remote Fall Prevention Program vs. Face-to-Face in Low-medium Risk Elderly- A Cross Over Randomized Controlled Trial
Falls are a serious problem in the elderly leading to injuries, morbidity, and consequently a heavy impact on the individual suffering, and society at large.
This study aims to investigate the effectiveness of a remote fall prevention program in comparison with a similar face-to-face program. This study design is a randomized control trial (RCT) with a cross-over in group allocation. The population will include 106 home-dwelling elderly, aged 65 years or more, with low to moderate risk of fall. Participants will be randomized to start intervention in the remote or face-to-face group. Training will be twice weekly for 3 months, after which there will be two weeks of washout, followed by a cross-over between groups. Outcome measures will include fall rate over a year (primary measure), balance, functional testing, subjective measures of fear of falls, quality of life, satisfaction from intervention, adherence, and compliance.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of the proposed study is to investigate the effectiveness of a remote fall prevention training program. The proposed intervention program includes an Otago-based fall prevention training program to improve lower extremity strength, balance, and walking, directed by physical therapists, over 6 months. The remote group will train at home, using video communication software, while the face-to-face group will train at a local community center.
The proposed study will be designed as a randomized control trial (RCT) with a cross-over design. The population will include 106 home-dwelling elderly, aged 65 years or more, walking independently, that will be identified at low to moderate risk of fall. Candidates with unbalanced systemic disease or disorders, cognitive and physical Impairments that will prevent participation in the program, will not be included. A full description of the inclusion and exclusion criteria is provided below in the Eligibility section.
Participants will be randomized into two groups that will receive similar Otago-based fall prevention group training, either remotely or face-to-face.
The training sessions: The training starts with five minutes of gentle warm-up with the same five flexibility exercises, followed by structured lower limb muscles strengthening, balance exercises, and instruction for independent walking for up to 30 minutes at least twice a week. The training will be delivered to groups of ten participants. The duration of each session will be one hour, twice a week for three months. After three months of training, there will be a two weeks break, serving as a washout period, after which the groups will switch, for another three months. At the end of the intervention period (6.5 months), each participant will be trained by both remote and face-to-face programs. Assessments will be conducted at 4-time points: baseline, 3 months after completion of the first-ordered training, 6.5 months after completion of both trainings, and 12 months follow up.
The primary outcome measure is the number of falls during a year. secondary outcome measures include Objective measures as balance, Walking speed, lower extremities functional strength, adherence, and compliance to the training program. The subjective outcome measure will include participant Satisfaction from the program, Fear of falls, and Quality of life. More details regarding outcome measures are provided below in the outcome measure section.
Statistical analysis: The equivalence test will be used to examine if the remote fall prevention training is as good as the face-to-face. In order to check if there is a period-treatment effect on the objective outcome measures we will employ a mixed-model repeated-measures analysis of variance (ANOVA): 4-time points (baseline, 3 months, 6 months, 12 months follow up) X 2 interventions (remote vs. face-to-face), counting for the fact that subjects are nested in sequence. When interaction will be significant simple mean analysis will be used to reveal a significant source. Studentized Maximum Modulus (SMM) post-hoc adjustment method will be used to reveal significance between pairs of periods.
If this study will manage to show remote fall prevention is feasible, safe, and effective, it will promote a solution in one of the most serious health problems in the elderly, in one of the most challenging eras for the elderly, when remote healthcare is vital.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Haifa, Israel
- The Faculty of Social Welfare and Health Science, Haifa University
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Kfar vradim, Israel, 2017000
- Gold club Kfar vradim
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- home-dwelling elderly, aged 65 years or more
- Identified to be at low to moderate risk of falling
Risk of falling will be assessed according to a combination of subjective and objective evaluation. Subjective questions from the STEADI (stopping elderly accidents death, and injuries), an algorithm for fall risk screening, assessment, and intervention, developed by the American Center for Disease Control and Prevention, relate to (1) Feels unsteady when standing/walking, (2) Worries about falling, and (3) Has fallen no more than 3 times in the past year.
An additional inclusion criterion is scoring 21 or more in the Mini-Best test (a balance test).
Exclusion Criteria:
- Subjects suffering from severe musculoskeletal pain or disorders that will limit completion of the assessment procedure such as pain limiting weight-bearing for no longer than a few minutes
- Unstable cardiovascular/pulmonary disease
- Unbalanced diabetes
- Neurological diseases such as stroke, Parkinson's, or multiple sclerosis
- Use of a walking aid (except for a cane)
- visual or hearing impairment that will not allow the use of technology for remote practice
- A score lower than 21/30 on the Montreal Cognitive Assessment score (MoCA),
- High risk of falling on the balance test (Mini-BESTest ≤ 20)
Comment: exclusion criteria will be based on self-report and completed at the initial baseline assessment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Fall prevention intervention program conducted through telehealth
The training program is based on the principles of the Otago program, designed specifically to prevent falls.
It consists set of leg muscle strengthening and balance retraining exercises progressing in difficulty, and a walking plan.
The training will be delivered to a group of 10 participants.
Each participant will practice from home, using a zoom system.
The duration of each training will be one hour, the frequency of training will be twice a week for three months.
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balance and strength exercises
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Active Comparator: Similar fall prevention intervention program conducted through face to face group training
The training program is based on the principles of the Otago program, designed specifically to prevent falls.
It consists set of leg muscle strengthening and balance retraining exercises progressing in difficulty, and a walking plan.
The training will be delivered to a group of 10 participants.
The training sessions will be delivered at the local community center, twice a week for one hour for three months.
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balance and strength exercises
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of falls during the study period
Time Frame: Falls will be monitored for one year
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Subjects will self-report falls weekly in a personal fall diary.
This will be supported by a telephone call from one of the investigators once a month.
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Falls will be monitored for one year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mini Balance Evaluation Systems Tests
Time Frame: Change from baseline at 3, 6 and 12 months
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Mini Balance Evaluation Systems Tests (Mini-BESTest) is a clinical balance assessment tool.
This test includes 14 items, each scored from 0 (severe balance impairment) to 2 (no balance impairment).
The maximal possible score is 28 points.
Higher scores indicate better balance performance.
A score of 20 points or below indicates a high fall risk.
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Change from baseline at 3, 6 and 12 months
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Time-Up and Go Test
Time Frame: Change from baseline at 3, 6 and 12 months
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The Timed Up and Go Test (TUG) assesses mobility, balance, and fall risk in older adults.
The test measures the time required for a subject to stand up from sitting on a chair, walk for 3 meters, turn, walk back, and sit down.
A score of 12 seconds or more indicates risk of falling in community dwelling adults.
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Change from baseline at 3, 6 and 12 months
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Berg Balance Scale
Time Frame: Change from baseline at 3, 6 and 12 months
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The Berg Balance Scale (BBS) is a 14- item objective measure that assesses static and dynamic balance, and fall risk in adults.
Each item is scored from 0 (unable to perform) to 4 (normal performance).
The maximal possible score is 56 points.
Any score from 0 to 36 indicate 100% fall risk for older adults.
The Berg Balance Scale (BBS) is widely used in clinical practice to predict falls in the older adults.
lately, due to ceiling effect, the use of BBS as a single measure to accurately predict future falls seems to be insufficient.
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Change from baseline at 3, 6 and 12 months
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Four Stage Balance Test
Time Frame: Change from baseline at 3, 6 and 12 months
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The 4-Stage Balance Test assess static balance at four standing positions, that get progressively harder to maintain.
The person is asked to hold a position for 10 seconds without moving his feet or supporting.
An older adult, who cannot hold the tandem stand, which is the forth position, for at least 10 seconds, is at increased risk of falling.
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Change from baseline at 3, 6 and 12 months
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Walking speed
Time Frame: Change from baseline at 3, 6 and 12 months
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Walking speed will be measured using the 4-Meter Walk Test in seconds.
Walking speed lower than 1.0 seconds/meter is considered a strong predictor of falls in the elderly population living in the community.
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Change from baseline at 3, 6 and 12 months
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Lower extremities functional strength
Time Frame: Change from baseline at 3, 6 and 12 months
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Functional strength of the lower limbs will be measured by the 30-second Sit to Stand Test.
This is also used for fall prediction.
A result lower than expected by age and sex indicates a risk of falls
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Change from baseline at 3, 6 and 12 months
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Attendance
Time Frame: Will be monitored and record in any session time, for 6 months
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Attendance to the program will be recorded each class by the physiotherapist who will conduct the training.
Total attendance will be defined as the number/percentage of classes attended out of the total number of sessions conducted, for example attending 75 sessions out of 100 will be calculated as total attendance of 75%.
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Will be monitored and record in any session time, for 6 months
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Completion (retention)
Time Frame: Will be monitored and record in any session time, for 6 months
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Completion of the full period of the program- 6 months, will be recorded for each participant, and will reflect retention.
Non-completion will be recorded for the participants who will withdrawal from the program before the end of the program, and will not complete the 6 months, end of program, assessment.
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Will be monitored and record in any session time, for 6 months
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Satisfaction from program
Time Frame: Twice- after each program session (after 3 and 6 months).
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Participant satisfaction will be assessed using a satisfaction rating scale of 0-10, with a score of 0 indicating complete dissatisfaction and a score of 10 maximum satisfaction.
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Twice- after each program session (after 3 and 6 months).
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Fear of falls
Time Frame: Change from baseline at 3, 6 and 12 months
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Fear of falls will be assessed using the Modified Falls Efficacy Scale (MFES) questionnaire, which is one of the most common and reliable research tools in fall research.
In this questionnaire, the subject rates his confidence in performing 10 daily tasks
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Change from baseline at 3, 6 and 12 months
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12-Item Short Form Survey (SF-12) Quality of life questionnaire
Time Frame: Change from baseline at 3, 6 and 12 months
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Quality of life will be assessed using the SF-12 questionnaire.
This questionnaire assesses the perception of quality of life through 12 questions that relate to the subject's views about his state of health and ability to perform various actions and functions.
The use of this questionnaire is common in fall studies.
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Change from baseline at 3, 6 and 12 months
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
General Publications
- Sherrington C, Fairhall NJ, Wallbank GK, Tiedemann A, Michaleff ZA, Howard K, Clemson L, Hopewell S, Lamb SE. Exercise for preventing falls in older people living in the community. Cochrane Database Syst Rev. 2019 Jan 31;1(1):CD012424. doi: 10.1002/14651858.CD012424.pub2.
- Kyrdalen IL, Moen K, Roysland AS, Helbostad JL. The Otago Exercise Program performed as group training versus home training in fall-prone older people: a randomized controlled Trial. Physiother Res Int. 2014 Jun;19(2):108-16. doi: 10.1002/pri.1571. Epub 2013 Dec 11.
- Bernocchi P, Giordano A, Pintavalle G, Galli T, Ballini Spoglia E, Baratti D, Scalvini S. Feasibility and Clinical Efficacy of a Multidisciplinary Home-Telehealth Program to Prevent Falls in Older Adults: A Randomized Controlled Trial. J Am Med Dir Assoc. 2019 Mar;20(3):340-346. doi: 10.1016/j.jamda.2018.09.003. Epub 2018 Oct 23.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
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
- Remote fall prevention
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
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