FES Implementation Pediatrics
- Conditions
- Cerebral Palsy (CP)
- Registration Number
- NCT06689007
- Lead Sponsor
- University Health Network, Toronto
- Brief Summary
Physical rehabilitation interventions that promote activity-dependent neuroplasticity are desired for children with CP as this will result in improved motor skill and function. In adult neurological populations, such as stroke and spinal cord injury, FES is a recommended, evidence-based intervention that addresses motor and sensory impairments and promotes neuroplasticity. The evidence base supporting the safety, feasibility and efficacy of FES for youth with CP is rapidly growing, yet FES is not commonly used in Canadian pediatric rehabilitation. Through interviews with Canadian pediatric physical and occupational therapists, we identified numerous barriers to FES implementation, including a lack of knowledge and training in FES, difficulty accessing FES equipment, and a perceived lack of time to deliver FES within a treatment session. To address these barriers, we have developed an implementation intervention for FES that consists of an online course and toolkit for physical and occupational therapists. As a next step, we will evaluate the effects of the implementation intervention on pediatric therapists' knowledge, confidence and use of FES.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 18
- Licensed to practice physical or occupational therapy in Canada.
- Report that CP comprises ≥20% of their caseload over the past year.
- Has not previously taken a continuing education course in FES.
- Reports never (0% of treatment sessions) or rarely (1-20% of treatment sessions) using neuromuscular electrical stimulation (NMES) or FES in their clinical practice.
- Report being able to participate in a six-week online FES course from October 18 2024 - November 28 2024.
- Able to complete the course and interview in English.
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method FES knowledge quiz From pre-intervention to immediately post-intervention and six months post-intervention FES Confidence Questionnaire From pre-intervention to immediately post-intervention and six months post-intervention FES Use Survey From pre-intervention to immediately post-intervention and six months post-intervention Technology Assistance Model 2 Questionnaire From pre-intervention to immediately post-intervention and six months post-intervention Semi-structured Interview Six months post-intervention Guided by the RE-AIM Framework
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Toronto
🇨🇦Toronto, Ontario, Canada