- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07304180
Exergame vs Balance Training in Hemiplegia
Comparison of the Effects of Balance Exercises and Video Game-Based (Exergame) Exercises in Hemiplegia Rehabilitation
Hemiplegia rehabilitation is a long and demanding process, but with the right approach and patience, it is possible to regain lost functions and improve quality of life. Balance plays a critical role in helping stroke survivors regain independence. This randomized controlled study aims to compare the effects of balance exercises and video-based exergame training, in addition to conventional physiotherapy, on lower extremity functionality, balance, gait, daily living activities, quality of life, and fear of falling in patients with hemiplegia following stroke.
A minimum of 30 eligible participants will be randomly assigned to two groups:
Group 1 (Balance Exercise Group): Conventional physiotherapy plus balance exercises.
Group 2 (Exergame Group): Conventional physiotherapy plus video-based exergame sessions using the Nintendo Switch Ring Fit Adventure.
Both interventions will be conducted twice a week for four weeks under the supervision of a physiotherapist. Assessments will be performed before and after the intervention using standardized scales.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hemiplegia rehabilitation is not only a process of regaining lost motor functions but also a journey toward restoring independence and self-confidence. Balance improvement is one of the key components of this process, as it directly influences gait, mobility, and daily life participation. With technological advancements, exergame-based interventions have emerged as engaging and motivating tools that can complement traditional rehabilitation programs.
This study aims to compare the effectiveness of balance exercise training and exergame-based exercise programs when added to conventional physiotherapy in stroke patients with hemiplegia. Participants who meet the inclusion criteria and provide informed consent will be randomly allocated into two groups (n ≥ 15 per group).
Group 1 (Balance Exercise Group): Participants will perform balance exercises twice a week for four weeks, in addition to their conventional physiotherapy program, under the supervision of a physiotherapist.
Group 2 (Exergame Group): Participants will perform exergame sessions using Nintendo Switch Ring Fit Adventure twice a week for four weeks, alongside the same conventional physiotherapy program.
Outcome measures:
Lower extremity motor function: Fugl-Meyer Assessment for Lower Extremity Balance: Berg Balance Scale Functional mobility and gait: Functional Reach Test, Timed Up and Go Test, 10-Meter Walk Test Activities of daily living: Modified Barthel Index Quality of life: Stroke Impact Scale Fear of falling: Falls Efficacy Scale-International Assessments will be conducted at baseline and after the four-week intervention. Data analysis will be performed using the Statistical Package for Social Sciences (SPSS). Continuous variables will be expressed as mean ± standard deviation, and categorical variables as frequency and percentage. Depending on the normality of data distribution, appropriate parametric or non-parametric tests will be applied, with the level of significance set at p ≤ 0.05.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Eyupsultan
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Istanbul, Eyupsultan, Turkey (Türkiye), 2022
- Halic University
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 25 and 70 years.
- Have experienced either hemorrhagic or ischemic stroke.
- At least six months have passed since the stroke event.
- Have a Modified Rankin Scale score of 2 or 3.
- Able to stand independently.
- Able to walk at least 10 meters independently or with an assistive device.
- Able to sit and stand up independently.
- Have a Brunnstrom stage of at least 4 in both upper and lower extremities.
- Have a Brunnstrom stage of at least 3 in the hand.
- Have a Mini-Mental State Examination score greater than 24.
- Willing to voluntarily participate in the study.
Exclusion Criteria:
- History of more than one stroke.
- Participation in another exercise or rehabilitation program.
- Body Mass Index greater than 29.9.
- Cognitive, visual, or auditory impairments that interfere with -communication.
- Presence of other neurological disorders such as multiple sclerosis, Parkinson's disease, or spinal cord injury.
- Vestibular system disorders affecting balance (e.g., vertigo, CANVAS syndrome).
- Severe contractures, joint complications affecting movement, recent fractures, arthritis, or use of medications that may impair physical function.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1_Balance Exercise Group
Participants in this group will receive conventional physiotherapy combined with balance exercise sessions twice a week for four weeks under the supervision of a physiotherapist.
|
Participants in this group will perform balance exercise sessions in addition to conventional rehabilitation. These sessions will be conducted twice a week for four weeks, with each session lasting approximately 15-20 minutes. Weeks 1-2: Weight shifting in parallel bars, marching in place within parallel bars, mini squats while holding the bars, tandem stance, and tandem and lateral walking in parallel bars. Week 3: Controlled weight shifting outside the parallel bars, tandem stance, marching in place, mini squats against a wall, backward walking in parallel bars, obstacle course walking, and kicking a stationary ball with the non-affected foot. Week 4: Picking up objects placed at different angles from a standing position, catching and throwing a ball, supported single-leg standing on the affected side, weight shifting on a balance board, kicking a moving ball with the non-affected foot, and obstacle walking tasks. |
|
Experimental: Group 2_Exergame Group
Participants in this group will perform video-based exergame sessions in addition to conventional rehabilitation.
The exergame intervention will be conducted using the Nintendo Switch Ring Fit Adventure game.
Sessions will take place twice a week for four weeks under the supervision of a physiotherapist.
|
Participants in this group will perform video-based exergame sessions in addition to conventional rehabilitation.
These sessions will be conducted twice a week for four weeks, with each session lasting approximately 15-20 minutes under the supervision of a physiotherapist, using the Nintendo Switch Ring Fit Adventure game.
The exergame program was designed by a specialist physiotherapist.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scale
Time Frame: Baseline and after 4 weeks
|
To assess postural control and fall risk.
The scale consists of 14 items scored from 0 to 4, with a total possible score of 56.
Higher scores indicate better balance ability.
Assessments will be performed at baseline and after 4 weeks of intervention.
Type: Continuous (Score range: 0-56)
|
Baseline and after 4 weeks
|
|
Functional Reach Test
Time Frame: Baseline and after 4 weeks
|
To measure dynamic balance and the ability to maintain a stable base of support while reaching forward.
The distance between the starting and ending hand positions is recorded in centimeters.
Higher values indicate better balance and lower fall risk.
Type: Continuous (Distance in cm)
|
Baseline and after 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fugl-Meyer Assessment for Lower Extremity
Time Frame: Baseline and after 4 weeks
|
Evaluates motor function of the lower extremity, including reflex activity, movement within and outside synergies, and coordination/speed.
The total score ranges from 0 to 34, with higher scores indicating better motor function.
|
Baseline and after 4 weeks
|
|
Timed Up and Go Test
Time Frame: Baseline and after 4 weeks
|
Assesses functional mobility and dynamic balance.
The time (in seconds) it takes to stand up from a chair, walk 3 meters, turn around, walk back, and sit down is recorded.
Shorter times indicate better mobility.
|
Baseline and after 4 weeks
|
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10-Meter Walk Test
Time Frame: Baseline and after 4 weeks
|
Measures walking speed over a 10-meter distance.
The average time (in seconds) of three trials is recorded.
Faster times indicate better walking performance.
|
Baseline and after 4 weeks
|
|
Modified Barthel Index
Time Frame: Baseline and after 4 weeks
|
Assesses independence in activities of daily living (e.g., feeding, dressing, mobility, toileting).
Scores range from 0 to 100, with higher scores indicating greater independence.
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Baseline and after 4 weeks
|
|
Stroke Impact Scale
Time Frame: Baseline and after 4 weeks
|
Evaluates quality of life after stroke across domains such as strength, hand function, mobility, daily activities, emotion, communication, participation, and memory.
Scores range from 0 to 100, with higher values reflecting better perceived health status.
|
Baseline and after 4 weeks
|
|
Falls Efficacy Scale-International
Time Frame: Baseline and after 4 weeks
|
Assesses fear of falling during daily activities.
The 16-item questionnaire is scored from 16 to 64, with higher scores indicating greater fear of falling.
|
Baseline and after 4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayşenur Çetinkaya, Halic University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Acetinkaya008
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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