An interventional study of The engineer-built system, video-game based Kinect sensor in Cerebral Palsy Children and Upper Extremity Problem, sponsored by Mahidol University. Status unknown at 1 site in Thailand. Open to participants aged 10 Years to 15 Years. Per ClinicalTrials.gov, last updated 2022-09-19.
Sponsored by Mahidol University · Not applicable, Interventional, and Treatment
There are 3 phase of the study. This registration is phase 2.2. This registration will conduct a randomized controlled trial study in the cerebral palsy children. Due to the limitation of period of time of grant, we changed the study type into pilot-randomization. Our new method of study will collect all of our study which previously separated into pilot and randomized controlled trial in just only one study "pilot-randomization".
750 studies on the registry are indexed under Paralysis; 133 are open to participants now.
This study's planned enrollment of 48 is above the median of 30 across 537 interventional studies indexed under Paralysis.
Browse Paralysis studies →Mahidol University is the lead sponsor of 730 studies on the registry; 118 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Children in this arm will play the computer game which was developed by the researcher team 3 session/weeks for 5 weeks. Each session will last for 40 minutes.
Device: The engineer-built system, video-game based Kinect sensor
children in this arm will receive a conventional program by occupational therapists 3 times/week for 5 weeks. Each session will last for 40 minutes.
The games were developed by the researcher team.
Also known as: conventional occupational therapy program
range of motion
The range or motion of shoulder, elbow and wrist will be assessed by goniometer. The assessment will be done before starting the intervention as the baseline and then after finishing the intervention to detect change of range of motion from the the baseline. The range of motion will be reported in degrees.
Time frame: before starting the intervention and after finishing the intervention within 1 week
Box and block test
The name 'box and block test' is an unabbreviated scale title. The minimum score is zero and the maximum score is infinity.
Time frame: before starting the intervention and after finishing the intervention within 1 week
ABILHANDS-Kids
The ABILHANDS-kids is the name of the test. It is not an unabbreviated name. The children will be asked the difficulty of doing their activities of daily living by using 21 questionnaires. The rating of difficulties were impossible, difficult and easy. Then the rating would be score as impossible=0, difficult=1 and easy = 2. The analysis of the score of there items will use the Rasch analysis which it is available online on http://rssandbox.iescagilly.be/\~abilhand-kids-cerebral-palsy-en.html. The minimum score means a worse outcome and the maximum score means the better outcome.
Time frame: before starting the intervention and after finishing the intervention within 1 week
EQ-5D-Y
The EQ-5D-Y is a questionnaire which has 2 parts for a participants to complete. There are 5 questions asking in first part: mobility, looking after myself, doing usual activities, having pain or discomfort and feelin worried, sad or unhappy. The participant needs to rate these questions in 3 rating score: no problem, with some problem or with a lot of problem. The rating score will be coded as no problem=1, with some problem = 1 and with a lot of problem = 2. The code 11111 is the best condition and the code 33333 is the worst condition. The second part of the questionnaire is the EQ-VAS which the participants need to rate their condition on the linear scale from 0-100. The worst condition is score 0 and the best condition is score 100.Then the coding from the first part will be converted as an index value.
Time frame: before starting the intervention and after finishing the intervention within 1 week
Plan to share: Yes — I plan to share the result with the statistician and some researcher for the analysis. The sharing could not be track to the patient identification.
Supporting information: Sap
This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.
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Mahidol University