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Clinical Trials/NCT05251571
NCT05251571
Completed
Not Applicable

Efficacy of Video-Based Balance and Coordination Exercises in Individuals With Stroke

Muğla Sıtkı Koçman University1 site in 1 country30 target enrollmentAugust 1, 2022
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Muğla Sıtkı Koçman University
Enrollment
30
Locations
1
Primary Endpoint
ABC
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of the study is to compare the video-based balance coordination exercise program and the video-based conventional exercise program in patients with subacute stroke.

Detailed Description

Thanks to telerehabilitation, it will be possible for individuals to learn the exercise programs in the most appropriate way and to communicate easily with their physiotherapists with video images. In this way, it will be ensured that individuals can perform their exercises at the optimum level in non-clinical environments. The aim of the study is to compare the conventional home exercise program performed with video-based telerehabilitation and the balance coordination program in subacute stroke patients.

Registry
clinicaltrials.gov
Start Date
August 1, 2022
End Date
April 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Muğla Sıtkı Koçman University
Responsible Party
Principal Investigator
Principal Investigator

Fatih Ozden

Principal Investigator

Muğla Sıtkı Koçman University

Eligibility Criteria

Inclusion Criteria

  • Male and female patients aged 40 - 65 years
  • Having been diagnosed with stroke by a specialist physician and at least 3 months and maximum 6 months have passed since the diagnosis
  • No serious medical complications
  • Being able to understand verbal and visual commands
  • Getting at least 24 points on the mini mental state test
  • Able to walk at least 10 m without assistance using crutches or a walker
  • Having signed the consent form

Exclusion Criteria

  • Situations that will prevent assessments or communication with the individual
  • Being on psychotropic medication
  • People with ataxia or any other cerebellar symptoms
  • Other problems that would preclude evaluation and/or treatment

Outcomes

Primary Outcomes

ABC

Time Frame: Change from Baseline ABC at 6 weeks

This scale includes 16 tasks related to indoor and outdoor activities of daily living to measure balance confidence in the elderly with various levels of function. Higher scores indicate more confidence. ABC is scored from 0 to 100. Higher scores indicate higher function.

SSEQ

Time Frame: Change from Baseline SSEQ at 6 weeks

The 13-item SSEQ is used to measure participants' self-efficacy levels in performing daily functional activities and self-management. SSEQ is scored from 0 to 130. Higher scores indicate higher confidence.

FES-I

Time Frame: Change from Baseline FES-I at 6 weeks

There are 16 items in FES-I that assess the fear of falling during daily activities. FES-I is scored from 0 to 64. Higher scores indicate higher concerns about falling.

Secondary Outcomes

  • TSQ(Change from Baseline TSQ at 6 weeks)

Study Sites (1)

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