CHRIST program to improve upper arm function in children after stroke

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study delivers Comprehensive Hand Repetitive Intensive Strength Training (CHRIST), a high-repetition, strength-based, goal-oriented therapy targeting upper limb coordination and use in pediatric stroke survivors. Children aged 7–12 with clinical upper limb motor impairment receive structured therapy sessions and their manual ability is measured before and after the intervention using the ABILHAND-Kids questionnaire. Participants with recent intensive upper limb therapy, uncontrolled seizures, severe cognitive/behavioral impairments, or orthopedic limitations are excluded. The study is conducted at clinical sites that treat pediatric stroke patients in Mandi Bahāuddīn, Punjab Province.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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.

Where it's running

• Clinical settings having pediatric stroke patients.
  Mandi Bahāuddīn, Punjab Province, Pakistan Recruiting

Study contacts

• Principal investigator: Mashar Hayat, MS — Riphah International University, Lahore
• Study coordinator: Imran Amjad, Phd
• Email: imran.amjad@riphah.edu.pk
• Phone: 03324390125

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.