Comparing hydrotherapy and aerobic exercise for lung function in children with hemiplegic cerebral palsy
Improvement of Pulmonary Function in Hemiplegic Cerebral Palsied Children by Using Hydrotherapy and Aerobic Exercises
This study is testing whether hydrotherapy or aerobic exercise can improve lung function in children with hemiplegic cerebral palsy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 3 (estimated) |
| Ages | 8 Years to 16 Years |
| Sex | All |
| Sponsor | South Valley University Academic / other |
| Locations | 1 site (Giza, Faisal) |
| Trial ID | NCT06086678 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of hydrotherapy versus aerobic exercise on pulmonary function in children aged 8 to 16 with hemiplegic cerebral palsy. Sixty participants will be divided into three groups: one receiving only conventional physical therapy, another undergoing hydrotherapy, and the last participating in aerobic exercise. Pulmonary function will be assessed using the Six-minute walk test and spirometry before and after a 12-week treatment program consisting of three sessions per week. The goal is to determine which intervention leads to better respiratory outcomes.
Who should consider this trial
Good fit: Ideal candidates are children aged 8 to 16 with hemiplegic cerebral palsy who are clinically stable and able to follow instructions.
Not a fit: Patients with significant visual or auditory defects, other neurological issues, or cardiopulmonary dysfunction may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve pulmonary function and overall quality of life for children with hemiplegic cerebral palsy.
How similar studies have performed: Other studies have shown positive outcomes with similar interventions in improving physical function in children with cerebral palsy, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages ranged from 8 to 16 years. * Belonged to levels I to II of the Gross Motor Function Classification System (GMFCS). * Spasticity ranged from grade 1 to grade 1+ according to Modified Ashwarth Scale. - Able to walk, no impairment of sensation or other neurological or psychological problems. * Clinically and medically stable and able to understand and follow the instructions Exclusion Criteria: i) Visual and/or auditory defects. ii) Significant shortening and/or deformity of lower extremities. iii) Other neurological problems that affect balance or mentality (e.g. epilepsy) iv) Advanced radiographic alterations comprise (bone destruction, bony ankylosis, knee joint sublaxation as well as epiphysial fracture). v) Lower extremity skeletal abnormalities (whether congenital or acquired). vi) Cardiopulmonary dysfunction.
Where this trial is running
Giza, Faisal
- Ragaee Saeed Mahmoud — Giza, Faisal, Egypt (Recruiting)
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.