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

Not Applicable
Completed
Conditions
Cerebral Palsy
Registration Number
NCT02801279
Lead Sponsor
National Taiwan University Hospital
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Performance change of Kinematic analysisbaseline, after 8 weeks, after 6 months
Secondary Outcome Measures
NameTimeMethod
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 Building Tower Test (BTT)baseline, every week(week1 to week 8), after 4 weeks, after 8 weeks, after 6 months
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 Satisfactory Questionnaire (SQ)baseline, 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 String Beads Test (SBT)baseline, every week(week1 to week 8), 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
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

Trial Locations

Locations (1)

National Taiwan University Hospital

🇨🇳

Taipei, Taiwan

National Taiwan University Hospital
🇨🇳Taipei, Taiwan

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