Actively Recruiting
Effectiveness of Smartphone-Based Versus Community-Based Otago Exercise Programs for Fall Risk Reduction in Community-Dwelling Older Adults: A Randomized Controlled Trial
Led by Binghamton University · Updated on 2026-02-25
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying ways to reduce falls in older adults by comparing two methods of delivering the Otago Exercise Program (OEP), a proven fall prevention exercise routine that focuses on muscle strengthening and balance. The study aims to bridge the gap between research and community use by testing a smartphone-based home program against a traditional in-person community program. This research also looks at how practical, acceptable, and easy to use each delivery method is for older adults at risk of falling. Participants who are at intermediate or high risk of falling will be randomly assigned to one of two groups: a smartphone-based program delivered through an app with weekly phone support, or an in-person group exercise program at a community center. Both groups will undergo individualized 60-minute training sessions twice a week for eight weeks, following the structure of the OEP. The smartphone group will use an app to track and review exercises, while the community group will exercise together under professional guidance. Throughout the study, participants will complete various tests and surveys before and after the program, including balance and mobility assessments, depression scales, and fall risk evaluations. Gait speed will be measured weekly via smartphone. Researchers will monitor outcomes such as gait velocity and physical performance to assess the effectiveness of each delivery mode. The total participation includes the 8-week training and follow-up assessments, with testers and trainers blinded to group assignments and baseline results.
CONDITIONS
Brief Title
Comparison of Smartphone and Community-Based Delivery of the Otago Exercise Program for Fall Risk in Older Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Community-dwelling older adults 55 years of age or older
- Ability to communicate in English
- Ability to walk at least 10 meters with or without an assistive device
- Cognitive function intact with a Montreal Cognitive Assessment (MoCA)-Blind score of 18/22 or greater
- Access to an Android or iOS smartphone
- Classified as intermediate or high risk of falling based on World Guidelines for Falls Prevention
You will not qualify if you...
- Lower limb amputation
- Visual impairment not correctable with lenses
- Uncontrolled hypertension, diabetes, neurological or musculoskeletal impairment
- Persistent dizziness or lightheadedness
- Spine or lower-extremity surgery within the past 12 months
- Self-reported pain greater than 7 on a scale of 0-10
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive individualized 60-minute training sessions of the Otago Exercise Program two times per week for eight weeks, either remotely via a smartphone application or in-person in a community group setting. Weekly phone check-ins are provided for the smartphone group to ensure safety and adherence.
16 training sessions over 8 weeks; weekly phone check-ins for smartphone group
Duration - 1 week post intervention
Participants complete post-intervention assessments including surveys and physical function tests to evaluate outcomes. Gait speed is assessed weekly using smartphone-based measurements during the intervention period.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Binghamton University
Binghamton, New York, United States, 13902
Actively Recruiting
Research Team
V
Vipul Lugade, PhD
P
Patima Silsupadol, PT, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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