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CompletedNCT05251571Updated Apr 4, 2023

The Efficiency of Video-Based Exercises in Individuals With Stroke

An interventional study of Conventional Exercise Group with Telerehabilitation and Balance Coordination Group with Telerehabilitation in Stroke, sponsored by Muğla Sıtkı Koçman University. Completed at 1 site in Turkey. Open to participants aged 40 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-04-04.

Sponsored by Muğla Sıtkı Koçman University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
40 Years to 65 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Stroke

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Keywords

  • Stroke
  • Telerehabilitation
  • Balance
  • Coordination
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 30 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Muğla Sıtkı Koçman University is the lead sponsor of 112 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Active comparator
    Conventional Exercise Group with Telerehabilitation

    Exercises such as muscle strengthening exercises applied to antigravity muscles, agonist antagonist spastic muscles, stretching exercises for spastic muscles, weight transfer will be applied, and a telerehabilitation platform will be used in the home exercise program.

    Other: Conventional Exercise Group with Telerehabilitation

  • Experimental
    Balance Coordination Group with Telerehabilitation

    Sit and stand exercise from chair, standing posture, weight transfer to right and left extremities, stepping over obstacles, standing on one leg with support from the table, standing on two legs with support from the table, hip abduction with support from the table, extension, flexion, supported tandem walking exercises such as stepping on the stairs, standing functional stretches will be applied. Whatsapp application-based Telerehabilitation platform will be used to deliver the home exercise program.

    Other: Balance Coordination Group with Telerehabilitation

Interventions

  • OtherConventional Exercise Group with Telerehabilitation

    Exercises such as conventional muscle strengthening and stretching given with telerehabilitation are applied.

  • OtherBalance Coordination Group with Telerehabilitation

    Functional muscle strengthening, stretching, balance and coordination exercises given with telerehabilitation are applied.

06

What researchers measure

Primary outcomes

  1. FES-I

    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.

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

  2. ABC

    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.

    Time frame: Change from Baseline ABC at 6 weeks

  3. SSEQ

    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.

    Time frame: Change from Baseline SSEQ at 6 weeks

Secondary outcomes

  1. TSQ

    This questionnaire consists of 14 items. The level of satisfaction of the patients with the software or system from which they receive treatment or other remote rehabilitation services is evaluated. TSQ is scored from 14 to 170. Higher scores indicate higher satisfaction.

    Time frame: Change from Baseline TSQ at 6 weeks

07

Study locations

1 site
  • Ege University Hospital Neurology Polyclinic
    İzmir, Bornova 35030, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 4, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05251571
Lead sponsor
Muğla Sıtkı Koçman University
Responsible party
Fatih Ozden (Principal Investigator, Muğla Sıtkı Koçman University) — Principal investigator
First posted
Feb 22, 2022
Start date
Aug 1, 2022
Primary completion
Feb 1, 2023
Completion
Apr 1, 2023
Last update
Apr 4, 2023

Study contacts

Mehmet Özkeskin, PhD
principal investigator · Ege University
İsmet Tümtürk, MSc
principal investigator · Ege University
Bedriye Karaman, MD
principal investigator · Ege University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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