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Clinical Trials/NCT03591185
NCT03591185
Unknown
Not Applicable

FallSensing Clinical Tool for Fall Risk Prevention in Community-dwelling Adults Aged 50 Years or Over

Anabela Correia Martins1 site in 1 country30 target enrollmentJuly 10, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Accidental Falls
Sponsor
Anabela Correia Martins
Enrollment
30
Locations
1
Primary Endpoint
Timed Up and Go
Last Updated
7 years ago

Overview

Brief Summary

Fall prevention programs should include strength and balance training, home hazard assessment and intervention, vision assessment and referral and also medication review with modification/withdrawal. Evidence exists that a tailored exercise program can reduce falls by as much as 54%.

Several studies recognize the benefits of the Otago Exercise Program (OEP) on physical functioning and falls reduction in older people. The program includes strength and balance exercises with a difficulty level progression by increasing weights and number of repetitions, in association with a walking plan.

FallSensing clinical tool includes a software, a pressure platform and two inertial sensors. The software includes a range of exercises based on Otago Exercise Program, including warming, balance and strength exercises. The software allows that healthcare professional prescribes a tailored exercise program according to the individual needs. During exercise performance, pressure distribution can be analysed by the healthcare professional, providing real time feedback to the individual.

Registry
clinicaltrials.gov
Start Date
July 10, 2017
End Date
October 31, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Anabela Correia Martins
Responsible Party
Sponsor Investigator
Principal Investigator

Anabela Correia Martins

Senior Lecturer Physiotherapy Dept.

Escola Superior de Tecnologia da Saúde de Coimbra

Eligibility Criteria

Inclusion Criteria

  • adults aged 50 years or over;
  • Community-dweller
  • independent to be standing and walking, with or without walking aids,
  • interest to participate in the study.

Exclusion Criteria

  • individuals with severe sensorial impairments (deafness or blindness)
  • individuals with cognitive impairments which precludes the ability to comprehend the questionnaire, functional tests and exercises included in the protocol.

Outcomes

Primary Outcomes

Timed Up and Go

Time Frame: Change from baseline time to perform TUG up to 12 weeks

seconds

Self-efficacy for Exercise

Time Frame: Change from baseline Self-efficacy for exercise score up to 12 weeks

Score 5 to 20 points

Secondary Outcomes

  • Grip Strength(Outset and up to 12 weeks)
  • 30 seconds Sit-to-Stand(Outset and up to 12 weeks)
  • Step Test(Outset and up to 12 weeks)
  • 4 Stage Balance Test "Modified"(Outset and up to 12 weeks)
  • 10 meters Walking Speed(Outset and up to 12 weeks)

Study Sites (1)

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