- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06352762
The Effects of Upper Extremity Robotic Rehabilitation in Children With Spastic Hemiparetic Cerebral Palsy
The Effects of Upper Extremity Robotic Rehabilitation on Upper Extremity Skills and Functional Independence Level in Patients With Spastic Hemiparetic Cerebral Palsy
Aims: To investigate the effects of upper extremity robotic rehabilitation on upper extremity skills and functional independence level in patients with hemiparetic Cerebral Palsy (hCP).
Methods: 34 hCP patients attended the study. 17 children in the training group recived conventional physiotherapy and Robotic Rehabilitation. 17 children in the control group recived only conventional physiotherapy. Convantional physiotherapy program lasted 45 minutes, Robotic Rehabilitation program lasted 30 minutes. All participants were enrolled in sessions 3 times a week for 5 weeks. Measurements were made before and after the therapy. Outcome measures were Modified Ashworth Scale (MAS) for muscle tone, Abilhand-Kids Test for manual skills, The Quality of Upper Extremity Skills Test (QUEST) for upper extremity motor function and The WeeFIM for functional independence level.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Nilüfer
-
Bursa, Nilüfer, Turkey, 16130
- Nuriye Büyüktaş
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosed with spastic hemiparetic CP
- Upper extremity muscle tone between 1-3 according to the Modified Ashworth Scale
- According to Gross Motor Functional Clasification System level 1-2-3
- Able to understand simple instructions
Exclusion Criteria:
- Having a history of epilepsy
- Having botox in the last 6 months
- Having surgery in the last 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Conventional physiotherapy
Strengthening and stretching exercises for lower and upper extremity muscles, hip and trunk stabilization training, balance training, gait training, upper extremity functional skills training, endurance training and coordination training were given.
|
Strengthening and stretching exercises for lower and upper extremity muscles, hip and trunk stabilization training, balance training, gait training, upper extremity functional skills training, endurance training and coordination training were given.
Exercises were planned according to the developmental stage.
Sessions were applied 3 days a week and 45 minutes for 5 weeks, for a total of 15 sessions.
|
|
Experimental: Robotic Rehabilitation
Strengthening and stretching exercises for lower and upper extremity muscles, hip and trunk stabilization training, balance training, gait training, upper extremity functional skills training, endurance training and coordination training were given.
In addition, upper extremity robotic rehabilitation was applied.
|
Strengthening and stretching exercises for lower and upper extremity muscles, hip and trunk stabilization training, balance training, gait training, upper extremity functional skills training, endurance training and coordination training were given.
Exercises were planned according to the developmental stage.
Sessions were applied 3 days a week and 45 minutes for 5 weeks, for a total of 15 sessions.
An additional 30 minutes of robotic rehabilitation was applied to the conventional physiotherapy program.
Robotic rehabilitation was applied after each session of conventional physiotherapy applications.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Tone
Time Frame: Assessment was performed twice, before treatment started and at the end of the fifth week.
|
Muscle tone was assessed using the Modified Ashworth Scale.
Resistance to passive movement was scored from 0 to 5. Higher scores indicate higher muscle tone.
Shoulder extensors, adductors and internal rotators; elbow flexors; forearm pronators, wrist and finger flexors were evaluated.
Each region was evaluated individually, and the sum of the measured regions was calculated to determine overall muscle tone.
|
Assessment was performed twice, before treatment started and at the end of the fifth week.
|
|
Upper Extremity Motor Function
Time Frame: Assessment was performed twice, before treatment started and at the end of the fifth week.
|
The Quality of Upper Extremity Skills Test (QUEST) was used.
The test evaluates dexterity and quality of movement.
It consists of a total of 7 headings (Independent movements, grasping, weight bearing, protective extension, degree of hand function, degree of spasticity, level of cooperation) and 34 items.
Each item is scored between 0-2.
A score of 0 indicates that the movement was not achieved, 1 point indicates that it was partially achieved, and 2 points indicates that it was completely achieved.
High scores from the test indicate good upper extremity motor functions.
|
Assessment was performed twice, before treatment started and at the end of the fifth week.
|
|
Manual Ability
Time Frame: Assessment was performed twice, before treatment started and at the end of the fifth week.
|
Abilhand-Kids test was used.
This test evaluates children's abilities in daily living activities for the hand and upper extremity.
The test consists of 21 items.
Each item is scored between 0-2.
A score of 0 means that the activity cannot be done, a score of 1 means that the child has difficulty in doing the activity, and a score of 2 means that the activity can be done easily.
High scores from the test indicate good manual abilities.
|
Assessment was performed twice, before treatment started and at the end of the fifth week.
|
|
Functional Independence
Time Frame: Assessment was performed twice, before treatment started and at the end of the fifth week.
|
It was assessed using the pediatric functional independence scale (WeeFIM).
It contains a total of 6 topics and 18 questions, including self-control, sphincter control, transfers, locomotion, communication, social and cognitive functions.
Each item is scored between 1-7.
High scores from the test indicate a high level of independence.
|
Assessment was performed twice, before treatment started and at the end of the fifth week.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nuriye Büyüktaş, MsC, Izmir Bakircay University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- Izmir Dokuz Eylul University
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
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Upper Extremity Paresis
-
Riphah International UniversityRecruitingUpper Extremity ParesisPakistan
-
Duke UniversityRecruitingStroke | Arm Weakness as a Consequence of Stroke | Upper Extremity Weakness | Upper Extremity Hemiparesis | Upper Extremity ImpairmentsUnited States
-
Adventist HealthCareCenter for Student Research Texas Woman's UniversityRecruitingStroke | Upper Extremity ParesisUnited States
-
University of the Sciences in PhiladelphiaThomas Jefferson University; Chapman University; Moss Rehabilitation Research...Active, not recruitingUpper Extremity ParesisUnited States
-
BaycrestCompletedStroke | Upper Extremity ParesisCanada
-
Adventist HealthCareTexas Woman's UniversityCompletedStroke | Upper Extremity ParesisUnited States
-
Ben-Gurion University of the NegevBarzilai Medical Center; Bet HadarCompletedUpper Extremity Paresis | Motor ControlIsrael
-
Weill Medical College of Cornell UniversityCompletedSurgery of Right Upper ExtremityUnited States
-
Abant Izzet Baysal UniversityThe Scientific and Technological Research Council of TurkeyRecruitingStroke | Upper Extremity Paralysis | Upper Extremity ParesisTurkey (Türkiye)
-
University of British ColumbiaUniversity of Toronto; Queen's University; Dalhousie University; Wings for LifeRecruitingUpper Extremity Dysfunction | Cervical Spinal Cord Injury | Spinal Cord Injury | Spinal Cord Injury at C5-C7 Level | SCI - Spinal Cord Injury | Upper Extremity Paralysis | Tetraplegia | Upper Extremity ParesisCanada
Clinical Trials on Conventional physiotherapy
-
Istanbul Demiroglu Bilim UniversityCompletedMuscle Weakness | Rehabilitation | Intensive Care Unit SyndromeTurkey
-
University of SalamancaCompleted
-
Pamukkale UniversityCompletedChronic Low-back PainTurkey
-
Kirsehir Ahi Evran UniversitesiEnrolling by invitation
-
International Hellenic UniversityRecruiting
-
Kutahya Health Sciences UniversityRecruitingAnterior Cruciate Ligament InjuriesTurkey
-
Bezmialem Vakif UniversityCompleted
-
University of LahoreRecruitingHypotonic Cerebral PalsyPakistan
-
Riphah International UniversityRecruitingLateral EpicondylitisPakistan
-
Eastern Mediterranean UniversityCompletedCervical SpondylosisCyprus