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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02801279
Enrollment
32
Registered
2016-06-15
Start date
2017-03-04
Completion date
2024-06-04
Last updated
2024-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy

Keywords

Cerebral Palsy, Occupational Therapy, Upper Limb Motor Training

Brief summary

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.

Interventions

OTHERConventional bilateral arm training

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

OTHERKinect-based bilateral arm training

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

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria of children with CP are: 1. diagnosed with congenital hemiplegic 2. no excessive muscle tone (Modified Ashworth Scale ≤ 3 at any joints of the upper limb) The

Exclusion criteria

of children with CP are: 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. The inclusion criteria of typically developing children are: 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. The

Design outcomes

Primary

MeasureTime frame
Performance change of Kinematic analysisbaseline, after 8 weeks, after 6 months

Secondary

MeasureTime frame
Score change of Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Pediatric Evaluation of Disability Inventory (PEDI)baseline, after 4 weeks, after 8 weeks, after 6 months
Change of muscle strengthbaseline, after 8 weeks, after 6 months
Score change of Melbourne Assessment 2 (MA-2)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Pediatric Motor Activity Log-Revised (PMAL-R)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of ABILHAND-Kidsbaseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Test of Playfulness (ToP)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of String Beads Test (SBT)baseline, every week(week1 to week 8), after 4 weeks, after 8 weeks, after 6 months
Score change of Engagement Questionnaire (EQ)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Satisfactory Questionnaire (SQ)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Building Tower Test (BTT)baseline, every week(week1 to week 8), after 4 weeks, after 8 weeks, after 6 months
Score change of Cerebral Palsy Quality of Life Questionnaire for Children (CPQOL)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Parenting Stress Index-Short Form (PSI-short)baseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Test of Visual Perceptual Skillsbaseline, after 4 weeks, after 8 weeks, after 6 months
Score change of Box and Block Test (BBT)baseline, every week(week1 to week 8), after 4 weeks, after 8 weeks, after 6 months

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026