MedPath

FES Implementation Pediatrics

Not Applicable
Active, not recruiting
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
Inclusion Criteria
  1. Licensed to practice physical or occupational therapy in Canada.
  2. Report that CP comprises ≥20% of their caseload over the past year.
  3. Has not previously taken a continuing education course in FES.
  4. Reports never (0% of treatment sessions) or rarely (1-20% of treatment sessions) using neuromuscular electrical stimulation (NMES) or FES in their clinical practice.
  5. Report being able to participate in a six-week online FES course from October 18 2024 - November 28 2024.
  6. Able to complete the course and interview in English.
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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
FES knowledge quizFrom pre-intervention to immediately post-intervention and six months post-intervention
FES Confidence QuestionnaireFrom pre-intervention to immediately post-intervention and six months post-intervention
FES Use SurveyFrom pre-intervention to immediately post-intervention and six months post-intervention
Technology Assistance Model 2 QuestionnaireFrom pre-intervention to immediately post-intervention and six months post-intervention
Semi-structured InterviewSix months post-intervention

Guided by the RE-AIM Framework

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Toronto

🇨🇦

Toronto, Ontario, Canada

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