CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 6 enrolled
Drug / intervention
RT 300-P FES Cycledevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00291317
NCT00291317N/ACompleted

The Effect of FES on Children With Spinal Cord Dysfunction

Children's Specialized Hospital·interventional·Posted Feb 14, 2006·Updated Aug 13, 2012

In Brief

A clinical study evaluating RT 300-P FES Cycle for Spinal Cord Injury. Completed, enrolled 6 participants.

Detailed Summary

Regular exercise is strongly recommended to help maintain a healthy lifestyle. Unfortunately, children and young adults with damaged spinal cords may not be able to exercise regularly. However, there is an exercise bike specially designed for persons with damaged spinal cords that enables them to pedal by directly stimulating the muscles in their legs. Our study is designed to determine the benefits of exercise for Spinal Cord Injured (SCI) patients using this bike.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 14, 2006
Enrollment StartJan 1, 2006
Primary CompletionSep 1, 2008
Study CompletionJan 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 20.4 years ago

Interventions

RT 300-P FES Cycledevice

Participants exercised using functional electrical stimulation cycling (FES) using the RT 300-P FES cycle (Restorative Therapies, Baltimore, MD). Children were scheduled to attend three cycling sessions per week on non-consecutive days for up to 30 minutes per session over a 9 month period. The intervention was provided at Children's Specialized Hospital in Mountainside, and families were required to provide their own transportation. During the study, the participants continued to participate in their standard, primary rehabilitation program.