To Evaluate the Efficacy of Mobile Applications in Tailoring and Enhancing Rehabilitation Interventions for Pediatric CP
NCT ID: NCT06428552
Last Updated: 2024-05-24
Study Results
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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ACTIVE_NOT_RECRUITING
NA
96 participants
INTERVENTIONAL
2023-11-01
2024-09-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Usual care at home for 12 weeks
Daily rehabilitation program of 40 minutes duration using a mobile application to be completed 6 days per week for 12 weeks
Mobile Application
Daily rehabilitation program of 40 minutes duration using a mobile application to be completed 6 days per week for 12 weeks
Interventions
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Mobile Application
Daily rehabilitation program of 40 minutes duration using a mobile application to be completed 6 days per week for 12 weeks
Eligibility Criteria
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Inclusion Criteria
* Children aged between 5 to 16 years
Exclusion Criteria
* undergone botulinum neurotoxin A (BoNT-A)injections or surgery in the previous 2 months or 6 months respectively. "
5 Years
16 Years
ALL
No
Sponsors
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Superior University
OTHER
Responsible Party
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Muhammad Naveed Babur
Principal Investigator
Locations
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Hope Rehabilitaion Centre, Mansoor Hospital Lahore , ChildRehab Sangla Hill
Lahore, , Pakistan
Countries
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Other Identifiers
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MSRSW/Batch-Fall22/712
Identifier Type: -
Identifier Source: org_study_id
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