Development of Kinect-assisted Home-based Bilateral Arm Training Program for Cerebral Palsy

NCT ID: NCT02801279

Last Updated: 2024-09-20

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

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-04

Study Completion Date

2024-06-04

Brief Summary

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The purpose of the present study is to develop a long term cost-effectiveness (efficient protocol, playful context, and practical strategy) training program for school-age children with Cerebral Palsy. Also, evaluate efficacy of Kinect-assisted bilateral arm training program for children with Cerebral Palsy.

Detailed Description

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Conditions

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Cerebral Palsy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Kinect-based bilateral arm training

The Kinect-based bilateral arm training focuses activities that required the use of both hands by using Kinect game.

Group Type EXPERIMENTAL

Kinect-based bilateral arm training

Intervention Type OTHER

The conventional bilateral arm training focuses activities that required the use of both hands.

Conventional bilateral arm training

The conventional bilateral arm training focuses activities that required the use of both hands.

Group Type EXPERIMENTAL

Conventional bilateral arm training

Intervention Type OTHER

The Kinect-based bilateral arm training focuses activities that required the use of both hands by using Kinect game.

Interventions

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Conventional bilateral arm training

The Kinect-based bilateral arm training focuses activities that required the use of both hands by using Kinect game.

Intervention Type OTHER

Kinect-based bilateral arm training

The conventional bilateral arm training focuses activities that required the use of both hands.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. diagnosed with congenital hemiplegic
2. no excessive muscle tone (Modified Ashworth Scale ≤ 3 at any joints of the upper limb)


1. absence of medical or developmental diseases which would affect physical and cognitive performances
2. having normal corrected vision
3. studying in regular education classroom in primary school for the 6-12 year-old children.

Exclusion Criteria

1. have severe cognitive, visual, or auditory disorders according to medical documents, parental reports, and the examiner's clinical observation
2. have injections of botulinum toxin type A.


(1) having score not within normal limits in BOTMP-short form
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Hao-Ling Chen

Role: PRINCIPAL_INVESTIGATOR

Taiwan University, Department of Occupational Therapy

Locations

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National Taiwan University Hospital

Taipei, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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201503112RIND

Identifier Type: -

Identifier Source: org_study_id

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