Functional Electrical Stimulation (FES) Cycling for Children With Spinal Cord Injuries (SCI)
|First Received Date ICMJE||October 27, 2005|
|Last Updated Date||January 29, 2009|
|Start Date ICMJE||March 2004|
|Primary Completion Date||June 2008 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
|Original Primary Outcome Measures ICMJE
|Change History||Complete list of historical versions of study NCT00245726 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE||Not Provided|
|Original Secondary Outcome Measures ICMJE||Not Provided|
|Current Other Outcome Measures ICMJE||Not Provided|
|Original Other Outcome Measures ICMJE||Not Provided|
|Brief Title ICMJE||Functional Electrical Stimulation (FES) Cycling for Children With Spinal Cord Injuries (SCI)|
|Official Title ICMJE||Lower Extremity Cycling With Functional Electrical Stimulation to Improve the Health and Fitness of Children With Spinal Cord Injuries|
The overall objective of this research project is to examine the clinical efficacy of lower extremity cycling with functional electrical stimulation to improve the health and fitness of children with spinal cord injuries (SCI). To achieve this goal, a controlled, randomized study will be conducted with thirty children who have sustained a spinal cord injury. The children in the study will be assigned to one of three groups: those receiving functional electrical stimulation (FES) leg cycling exercise, those receiving passive leg cycling, and a non-cycling control group receiving electrical stimulation therapy to generate muscle contractions in the lower extremity. All three groups will be balanced as to the amount of time they receive the specific therapy. All therapies, after initial assessment, will be conducted at home in order to foster changes in lifestyle that may prove to be essential for improved quality of life.
The specific aims of this proposal are delineated below:
Aim 1: To assess, by means of a randomized controlled study design, the ability of FES cycling to improve the cardiovascular and musculoskeletal systems of ten children with a spinal cord injury, as compared to ten children undergoing passive leg cycling exercise and ten children receiving electrical stimulation therapy alone.
Aim 2: To determine, by means of a randomized controlled study design, the feasibility of using FES leg cycling exercise to provide long-term health benefits and improve the neurologic status of ten children with a spinal cord injury, as compared to ten children undergoing passive leg cycling exercise and ten children receiving electrical stimulation therapy alone.
This is a controlled, randomized pretest/posttest study design in which three conditions will be compared: FES leg cycling exercise, passive leg cycling exercise, and a control group receiving electrical stimulation therapy. Randomization of the subjects into the three groups will be coordinated across the two sites. All other variables will be controlled to the extent possible. All children in this study will continue to receive standard therapy at the level established by the therapist working with the child. This includes passive stretching of the lower extremities and the use of standing frames. Medications will also remain unaltered throughout the study, unless changes in body mass or other physical conditions unrelated to the study (i.e. growth) warrant modification. All exercise sessions, after the initial one or two-week assessment, will be conducted at home.
Electrical activation of the muscles in this study will be achieved through the use of surface mounted electrodes. The muscle groups that will be electrically activated in this study are the quadriceps, the hamstrings, and the gluteal muscles bilaterally. This is based upon the previous FES cycling studies conducted in the adult population. The appropriate stimulation levels for each muscle will be determined for each subject.
All subjects in the three study groups, in addition to participation in this study, will receive standard therapy at home. For all of the children, this will include passive range of motion stretching three times each week. Ideally, stretching will be done before cycling or electrical stimulation therapy to act as a "warm-up" period before the more involved therapies are performed. For the children with sustained tetraplegia participating in this study, standard therapy will also involve standing three times each week, either with braces or the use of a standing frame.
FES Cycling Group The FES cycling group will be asked to participate in additional therapy involving cycling for thirty minutes, three times a week. All cycling movements will be accomplished with electrical activation of the leg muscles. The first one to two weeks will be conducted on-site to monitor the subjects' reaction to exercise, after which therapy sessions will continue at home. The goal will be achieving thirty minutes of continuous cycling at 50 rev•min-1 with zero power output. Until subjects reach this point, the cycling session will be divided into five to ten minute-long sets, separated by five-minute rest breaks. Each subject, however, will complete a total of thirty minutes of cycling at the set speed. Once subjects reach this point, the power output requirements will be increased. From the zero point, the power requirement for the first session will be increased by one watt (W). If the subject can cycle continuously for 30 minutes, the next session the power output requirement will be increased by one watt. If the subject cannot pedal for a full 30 minutes, the power requirement will be maintained at this higher level until 30 minutes of continuous cycling can be achieved. The power requirement will then be increased by one watt on the next session. Increases will continue in this manner until the end of the protocol, or until the maximum power output of 50 watts, has been reached.
Passive Cycling Group The passive cycling group will be asked to participate in additional therapy that will also involve cycling for thirty minutes, three times a week. However, the motor in the bicycle will provide all cycling movements. The first one to two weeks will be conducted on-site under the observation of the investigators, after which time therapy sessions will continue at home. The initial sessions will be used to determine whether the subject can tolerate the exercise, and to build fatigue resistance. The goal will be to achieve thirty minutes of continuous cycling at 50 rev•min-1 with zero power output. Once subjects can cycle for thirty minutes continuously, the subjects will continue at this level until the completion of the protocol.
Electrical Stimulation Therapy Group Subjects in the control group will maintain their standard therapy, in addition to receiving additional electrical stimulation therapy of the quadriceps and hamstring muscles for a period of 30 minutes, three times per week. The children in this group will act as a control group for the comparison of additional therapy time involving cycling, as compared to additional therapy time only. Electrical stimulation was selected as the additional therapy of choice since specific health and physiologic benefits have already been reported by this group of investigators and could thus be seen as comparable to cycling. Stimulation of the muscles will be accomplished using a portable, 2-channel surface stimulation unit (Empi, St. Paul Minnesota) instead of the ExoStim Unit. The hamstrings and quadriceps will be activated bilaterally for 15 minutes each at a level that produces a strong muscle contraction. This will be accomplished while the subjects are resting in the supine position, working against zero resistance. Attempts will also be made to incorporate the gluteal muscles into the electrical stimulation protocol, but the sessions will not exceed the thirty-minute time period.
|Study Type ICMJE||Interventional|
|Study Phase||Not Provided|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
|Condition ICMJE||Spinal Cord Injury|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Completed|
|Completion Date||June 2008|
|Primary Completion Date||June 2008 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||5 Years to 15 Years (Child)|
|Accepts Healthy Volunteers||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||United States|
|Removed Location Countries|
|NCT Number ICMJE||NCT00245726|
|Other Study ID Numbers ICMJE||SHC-8540|
|Has Data Monitoring Committee||No|
|U.S. FDA-regulated Product||Not Provided|
|Plan to Share Data||Not Provided|
|IPD Description||Not Provided|
|Responsible Party||Richard T. Lauer, Shriners Hospitals for Children|
|Study Sponsor ICMJE||Shriners Hospitals for Children|
|Collaborators ICMJE||Not Provided|
|Information Provided By||Shriners Hospitals for Children|
|Verification Date||January 2009|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP