Investigating dry needling for spasticity and functional ability in cerebral palsy
Effects of Dry Needling on Spasticity and Functional Ability in Children With Cerebral Palsy
This study is testing if dry needling can help improve movement and daily activities for people with cerebral palsy who have tight muscles.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 6 Years and up |
| Sex | All |
| Sponsor | Batterjee Medical College Academic / other |
| Locations | 1 site (Jeddah) |
| Trial ID | NCT06856473 on ClinicalTrials.gov |
What this trial studies
This study examines the effects of dry needling on spasticity and its impact on functional ability in individuals with cerebral palsy. Participants will undergo assessments using the Modified Ashworth Scale, Timed Up and Go test, and Gross Motor Function Measure to evaluate changes in muscle tone, mobility, and overall motor performance following the intervention. The goal is to determine whether dry needling can improve movement efficiency and functional outcomes for patients with spasticity. The findings aim to support the integration of dry needling into rehabilitation programs for neuromuscular disorders.
Who should consider this trial
Good fit: Ideal candidates are individuals with cerebral palsy exhibiting hypertonia and able to stand and walk independently.
Not a fit: Patients with significant cognitive deficits or severe uncontrolled epilepsy may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a new therapeutic approach to improve mobility and functional abilities in patients with spasticity.
How similar studies have performed: While dry needling is a relatively novel approach in this context, preliminary studies have shown promise in managing spasticity, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Hypertonia score 2 according to MAS * Able to understand and follow instructions * Able to stand and walk independantly Exclusion Criteria: * Participants with neurological conditions that involve significant cognitive deficits or severe uncontrolled epilepsy * Participants who have undergone surgical procedures within the last 3 months
Where this trial is running
Jeddah
- Bmc — Jeddah, Saudi Arabia (Recruiting)
Study contacts
- Study coordinator: Mohamed A Abdel Ghafar, PhD.
- Email: pt12.jed@bmc.edu.sa
- Phone: 966531513909
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.