Effects of CHRIST on Upper Limb Function in Children With Pediatric Stroke
Effects of Comprehensive Hand Repetitive Intense Strength Training on Upper Limb Function in Children With Pediatric Stroke
1 other identifier
interventional
15
1 country
1
Brief Summary
Pediatric stroke poses significant challenges due to its impact on a child's developing brain. Both ischemic and hemorrhagic strokes in children can result in long-term motor, sensory, and cognitive impairments, particularly affecting upper limb function. Comprehensive Hand Repetitive Intensive Strength Training is a structured intervention model that integrates high-repetition, strength-based, and goal-oriented exercises targeting upper limb coordination and use. This study aims to explore the efficacy of CHRIST in improving upper limb function using the ABILHAND-Kids questionnaire to assess changes in manual ability. The study aims to generate pediatric-specific evidence for intensive hand-focused rehabilitation strategies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable stroke
Started Feb 2026
Shorter than P25 for not_applicable stroke
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 4, 2026
CompletedFirst Submitted
Initial submission to the registry
February 23, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 30, 2026
February 27, 2026
February 1, 2026
6 months
February 23, 2026
February 23, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
ABILHAND-Kids
The ABILHAND-Kids is specifically developed to evaluate upper limb function in children and adolescents with neurological impairments, making them highly sensitive to changes in motor performance
Baseline and after 10 weeks
Study Arms (1)
CHRIST will be given to childrenwith pediatric stroke
EXPERIMENTALInterventions
A session of 40 minutes, which includes 3 sets (10 minutes exercise with 3 minutes rest period per set), three times a week, over a 10 weeks period. The speed of the treadmill for the upper limbs will be 0.3-1.2 km/h.
Eligibility Criteria
You may qualify if:
- Children aged 7 to 12 years diagnosed with pediatric ischemic or hemorrhagic stroke(21).
- Clinical evidence of upper limb motor impairment following stroke.
- Parent/guardian consent and child assent obtained.
You may not qualify if:
- Severe cognitive or behavioral impairments interfering with therapy.
- Uncontrolled seizures or medical conditions contraindicating exercise.
- Previous participation in intensive upper limb therapy within the last 3 months.
- Orthopedic conditions (e.g., fractures, contractures) that limit upper limb movement.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Clinical settings having pediatric stroke patients.
Mandi Bahāuddīn, Punjab Province, 5400, Pakistan
Related Publications (3)
Amlie-Lefond C, Sebire G, Fullerton HJ. Recent developments in childhood arterial ischaemic stroke. Lancet Neurol. 2008 May;7(5):425-35. doi: 10.1016/S1474-4422(08)70086-3.
PMID: 18420156BACKGROUNDKim DA, Lee JA, Hwang PW, Lee MJ, Kim HK, Park JJ, You JH, Lee DR, Lee NG. The Effect of Comprehensive Hand Repetitive Intensive Strength Training (CHRIST) Using Motion Analysis in Children with Cerebral Palsy. Ann Rehabil Med. 2012 Feb;36(1):39-46. doi: 10.5535/arm.2012.36.1.39. Epub 2012 Feb 29.
PMID: 22506234BACKGROUNDKabir R, Sunny MSH, Ahmed HU, Rahman MH. Hand Rehabilitation Devices: A Comprehensive Systematic Review. Micromachines (Basel). 2022 Jun 29;13(7):1033. doi: 10.3390/mi13071033.
PMID: 35888850BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mashar Hayat, MS
Riphah International University, Lahore
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 23, 2026
First Posted
February 27, 2026
Study Start
February 4, 2026
Primary Completion (Estimated)
July 30, 2026
Study Completion (Estimated)
August 30, 2026
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share