Skip to main content
Clinical Trials/NCT06689007
NCT06689007CompletedNot Applicable

Stimulating Change in Pediatric Rehabilitation: An Implementation Intervention to Increase Use of Functional Electrical Stimulation

University Health Network, Toronto1 site in 1 country15 target enrollmentStarted: October 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
15
Locations
1
Primary Endpoint
Semi-structured Interview

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •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
  • •Able to complete the course and interview in English.

Exclusion Criteria

  • Not provided

Arms & Interventions

Implementation Intervention

Experimental

Intervention: Implementation Intervention (Other)

Outcomes

Primary Outcomes

Semi-structured Interview

Time Frame: Six months post-intervention

Guided by the RE-AIM Framework

FES knowledge quiz

Time Frame: From pre-intervention to immediately post-intervention and six months post-intervention

FES Confidence Questionnaire

Time Frame: From pre-intervention to immediately post-intervention and six months post-intervention

FES Use Survey

Time Frame: From pre-intervention to immediately post-intervention and six months post-intervention

Technology Assistance Model 2 Questionnaire

Time Frame: From pre-intervention to immediately post-intervention and six months post-intervention

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kristin Musselman

Associate Professor

University of Toronto

Study Sites (1)

Loading locations...

Similar Trials