Effect of sensory stimulation on mobility in adults with cerebral palsy
Study of the Effect of Peripheral Somatosensory Stimulation on the Functionality of Patients With Cerebral Palsy and Reduced Mobility
This study is testing if sensory stimulation can help adults with cerebral palsy move better compared to just regular physical therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Facultat de ciencies de la Salut Universitat Ramon Llull Academic / other |
| Locations | 1 site (Barcelona) |
| Trial ID | NCT06951568 on ClinicalTrials.gov |
What this trial studies
This study evaluates how peripheral somatosensory stimulation can improve motor function in adults with cerebral palsy. It employs a crossover, randomized design where participants will alternate between receiving stimulation and standard physiotherapy. The study will involve 20 adults with reduced mobility, who will undergo a 12-week physical exercise program, with assessments conducted under both stimulation and non-stimulation conditions. The goal is to determine the effectiveness of sensory stimulation in enhancing mobility and functionality.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-50 with a medical diagnosis of cerebral palsy and reduced mobility classified as levels I, II, or III according to the GMFCS.
Not a fit: Patients with severe cognitive impairments or other medical conditions that may interfere with the intervention will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve mobility and quality of life for adults with cerebral palsy.
How similar studies have performed: While the specific approach of peripheral somatosensory stimulation may be novel, similar interventions have shown promise in improving motor function in other populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria * Adults with a medical diagnosis of cerebral palsy * Age: 18-50 years * Reduced mobility classified as levels I, II, or III according to the GMFCS * Ability to participate in functional assessments with the support of the clinical team * Ability to understand informed consent or have a legal representative who can provide consent on their behalf Exclusion Criteria * Patients with cerebral palsy who have severe cognitive impairments that hinder understanding of instructions or participation in assessments * Adults with cerebral palsy who present with medical conditions that may interfere with the intervention, such as severe cardiovascular disease or major neurological disorders * Individuals with cerebral palsy who are participating in another intervention study during the same period
Where this trial is running
Barcelona
- Pedro Victor López Plaza — Barcelona, Spain (Recruiting)
Study contacts
- Study coordinator: Pedro V López Plaza, Director
- Email: pedrovictorlp@gmail.com
- Phone: 932 53 32 56
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.