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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04516265
Other study ID # Okan U
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date July 21, 2020
Est. completion date September 21, 2021

Study information

Verified date August 2020
Source Okan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of our study is to compare the effects of NGT-based trunk training, video-based trunk training and video-based trunk training applied with Theratogs in children with hemiparetic type Cerebral Palsy.


Description:

The aim of our study is to compare the effects of NGT-based trunk training, video-based trunk training and video-based trunk training applied with Theratogs in children with hemiparetic type Cerebral Palsy. It is planned to include 45 patients with hemiparetic cerebral palsy between the ages of 5-15 and with Gross Motor Function Classification System (GMFCS) level I-III. Patients with cerebral palsy will be divided into 3 groups in a randomized controlled manner. Each group will continue and follow routine physiotherapy and rehabilitation treatments for 8 weeks. Then, structured trunk training will begin. NGT-based trunk training (45 minutes) to the first group, video-based trunk training (45 minutes) to the second group, and Video-based trunk training (45 minutes) will apply with Theratogs to the third group. Treatments will be applied two days a week for 8 weeks.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 45
Est. completion date September 21, 2021
Est. primary completion date July 21, 2021
Accepts healthy volunteers No
Gender All
Age group 5 Years to 15 Years
Eligibility Inclusion Criteria:

- Patients with I-III levels according to Communication Function Classification System

- Patients with I-III levels according to GMFCS

- Patients with Hemiparetic Cerebral Palsy

- Continuing regular physiotherapy and rehabilitation program for six months.

Exclusion Criteria:

- Presence of visual or auditory impairment

- Presence of epilepsy

- Patients who have undergone orthopedic surgery in the last 6 months

- Patients who received Botulinum Toxin-A injection in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
neurodevelopmental treatment
A personally designed treatment program will be applied in line with the principles of neurodevelopmental treatment.
video-based trunk training
Games developed for the use of children with cerebral palsy will be used for trunk training.
Video-based trunk training will apply with Theratogs
Video-based trunk training will apply with Theratogs

Locations

Country Name City State
Turkey Okan University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Okan University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Trunk Control Measurement Scale It will be used to evaluate trunk control in patients with CP. 8 weeks
Primary Trunk Muscle Tone Trunk Muscle Tone will be evaluated with the Myoton®PRO device. 8 weeks
Primary Segmental Assesment of Trunk Control Scale It is an evaluation method that allows the body control to be evaluated from 3 different aspects as static, active and reactive control, according to trunk control levels. 8 weeks
Primary Balance Assessment System The Fizyosoft Balance Assessment system, which works in harmony with the Nintendo Wii Balance Board, will be used in the assessment of the sitting balance. 8 weeks
Secondary Pediatric Berg Balance Scale It will be used to assess functional balance. 8 weeks
Secondary 10-meters walking test It will be used to evaluate walking. 8 weeks
Secondary Gillette Functional Gait Assessment Questionaire It will be used to evaluate functional walking. 8 weeks
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