MedPath

Effectiveness of Balance Training with a Special Device to Improve Stability in Older Adults

Phase 1
Not yet recruiting
Conditions
Geriatric Population
Registration Number
CTRI/2025/04/084838
Lead Sponsor
Rizwana Begum
Brief Summary

Participants will be selected based on inclusion and exclusion criteria, with informed consent obtained in their regional language. They will wear a safety harness to prevent falls during perturbation training. The Balance Perturbator device will use a perturbation intensity of 3 m/s² and an 18 cm displacement, based on existing safety and efficacy research. The intervention will last six weeks, with two sessions per week involving random perturbations in multiple directions. Postural sway will be measured using force plates and pressure sensors in the device.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Geriatric individuals with osteoarthritis of the knee joint will be included.
  • Community dwelling older adults with scores more than or equal to 13.5 seconds on Timed up and Go(TUG) test.
Exclusion Criteria

Diagnosed with Vertigo Recent fractures Cardiorespiratory Diseases Neurological/Neuromuscular disorders Any Musculoskeletal condition/disease Any cognitive impairment/Psychological disorder Any communication impairment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postural Sway measures like Sway path and Sway velocity of the Centre of Pressure(COP)Week 1 and Week 6
Secondary Outcome Measures
NameTimeMethod
Timed Up and Go (TUG) testWeek 1 and Week 6
Falls Efficacy Scale-InternationalWeek 1 and Week 6

Trial Locations

Locations (1)

SRM Medical College Hospital and Research Centre

🇮🇳

Kancheepuram, TAMIL NADU, India

SRM Medical College Hospital and Research Centre
🇮🇳Kancheepuram, TAMIL NADU, India
Rizwana Begum
Principal investigator
9004807912
rb4579@srmist.edu.in

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