Effects of Trunk Training in Patients With Cerebral Palsy

NCT ID: NCT04516265

Last Updated: 2020-08-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-21

Study Completion Date

2021-09-21

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cerebral Palsy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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NGT Group

A personally designed treatment program will be applied in line with the principles of neurodevelopmental treatment.

Group Type ACTIVE_COMPARATOR

neurodevelopmental treatment

Intervention Type PROCEDURE

A personally designed treatment program will be applied in line with the principles of neurodevelopmental treatment.

Video-based training group

Trunk training will be done with games developed for the use of children with cerebral palsy.

Group Type ACTIVE_COMPARATOR

video-based trunk training

Intervention Type PROCEDURE

Games developed for the use of children with cerebral palsy will be used for trunk training.

Video-based training group with theratogs

Video-based trunk training (45 minutes) will apply with Theratogs to the group

Group Type ACTIVE_COMPARATOR

Video-based trunk training will apply with Theratogs

Intervention Type PROCEDURE

Video-based trunk training will apply with Theratogs

Interventions

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neurodevelopmental treatment

A personally designed treatment program will be applied in line with the principles of neurodevelopmental treatment.

Intervention Type PROCEDURE

video-based trunk training

Games developed for the use of children with cerebral palsy will be used for trunk training.

Intervention Type PROCEDURE

Video-based trunk training will apply with Theratogs

Video-based trunk training will apply with Theratogs

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

5 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Okan University

OTHER

Sponsor Role lead

Responsible Party

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Derya Azim Rezaei

lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Derya Azim Rezaei, MSc

Role: PRINCIPAL_INVESTIGATOR

Okan University,Faculty of Health Sciences,Department of Physiotherapy and Rehabilitation

Burcu Ersöz Hüseyinsinoğlu, Associate professor

Role: STUDY_DIRECTOR

Istanbul University-Cerrahpaşa,Faculty of Health Sciences,Department of Physiotherapy and Rehabilitation

Locations

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Okan University

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Okan U

Identifier Type: -

Identifier Source: org_study_id

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