- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01244594
The Effects of Two Functional Electrical Stimulation Cycling Paradigms
Background:
People with spinal cord injury (SCI) are at risk for many health conditions, some of which can be decreased with exercise. Cycling with Functional Electrical Stimulation (FES) is one way to obtain exercise after SCI. However, cycling with FES has only been done one way, which involves pedaling more quickly with less force to work against. Pedaling more slowly would allow the person to work against more force, which may lead to greater improvements in bone mineral density and muscle size. It may also lead to greater changes in bone make-up, body fat, and cholesterol levels. All of these improvements may lead to a decrease in bone fractures and cardiovascular disease, two major medical issues that exist in the SCI population. Study Aims: This study will compare the outcomes on bone, muscle and cardiovascular health between the commonly used method of pedaling more quickly to a new method of pedaling more slowly. Both groups will work against the maximal force possible. It is expected that the group pedaling more slowly will work against greater force and thus will have improved outcomes compared to other group pedaling faster. Methods: Twenty people with SCI, ages 18-65 years, will be randomly assigned to a treatment group and will participate in three 60-minute sessions per week for 6 months at an outpatient rehabilitation center. All subjects must have complete paralysis of both legs, but may have sensation preserved. Before and after 6 months of exercise, subjects will have an MRI scan to assess muscle size and bone, a dexascan to assess bone, a strength test using electrical stimulation to assess muscle force, an analysis of fat free body tissue, and lab work to measure cholesterol, bone factors that provide insight into bone change, and nutritional status. Relevance: If the protocol of pedaling more slowly results in greater improvements, this technique can be applied to clinical practice. Some people with SCI have FES cycles in their homes and many have been cycling for many years. This new technique may allow them to obtain more benefits than what they currently are receiving from FES cycling. In addition, it is important to maintain overall bone, muscle and cardiovascular health so that people with SCI are health and ready when spinal cord regeneration becomes clinically available.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Phase 2
- Phase 3
Contacts and Locations
Study Locations
-
-
Pennsylvania
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Philadelphia, Pennsylvania, United States, 19107
- Thomas Jefferson University Hospital
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Philadelphia, Pennsylvania, United States, 19107
- Thomas Jefferson University
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Philadelphia, Pennsylvania, United States, 19102
- Magee Rehabilitation Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Cervical or thoracic SCI of greater than 6 months duration
- American Spinal Injury Association Impairment Scale (AIS) levels A (motor and sensory complete) or B (motor complete)
- Intact lower motor neurons to the quadriceps, hamstrings, and gluteal muscles
Exclusion Criteria:
- History of renal or bladder stones or renal impairment
- Presence of conditions that require chronic steroids
- Symptomatic or known cardiac disease
- Pulmonary disease limiting exercise tolerance
- Ventilator dependency
- Implanted devices that may be adversely affected by the FES system
- Lower extremity fragility fractures in the previous 3 months
- Severe spasticity in legs
- Presence of a Grade 2 or higher pressure ulcer
- Severely limited range of joint motion
- Heterotopic ossification of joints in the lower extremities
- Uncontrolled autonomic dysreflexia
- Dislocation of one or both hips
- Pregnancy or plans to become pregnant during the study
- Post menopausal, if female
- Current seizure disorder
- Participation in activities involving electrical stimulation or activity based therapy within the past 3 months
- Participation in a neuroregenerative intervention within the past 12 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: High cadence, low resistance
Subjects in this arm will cycle with functional electrical stimulation at a higher cadence (speed) and a lower resistance.
|
Subjects will cycle with functional electrical stimulation for one hour, 3 times per week at Magee Rehab's outpatient center.
Subjects will cycle for a total of 26 weeks (6 months).
|
|
EXPERIMENTAL: Low cadence, high resistance
Subjects in this arm will cycle with functional electrical stimulation at a lower cadence (speed) and a higher resistance.
|
Subjects will cycle with functional electrical stimulation for one hour, 3 times per week at Magee Rehab's outpatient center.
Subjects will cycle for a total of 26 weeks (6 months).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bone density and bone microarchitecture
Time Frame: Baseline
|
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
|
Baseline
|
|
Bone density and bone microarchitecture
Time Frame: 6 months
|
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
|
6 months
|
|
Muscle volume
Time Frame: Baseline
|
Muscle volume is assessed using MRI
|
Baseline
|
|
Muscle volume
Time Frame: 6 months
|
Muscle volume is assessed using MRI
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle strength
Time Frame: Baseline
|
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
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Baseline
|
|
Muscle strength
Time Frame: 3 months
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Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
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3 months
|
|
Muscle strength
Time Frame: 6 months
|
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
|
6 months
|
|
Bone markers
Time Frame: baseline
|
Bone markers are assessed through blood and urine analysis.
|
baseline
|
|
Bone markers
Time Frame: 3 months
|
Bone markers are assessed through blood and urine analysis.
|
3 months
|
|
Bone markers
Time Frame: 6 months
|
Bone markers are assessed through blood and urine analysis.
|
6 months
|
|
Fat free soft tissue
Time Frame: baseline
|
Fat free mass is assessed using a bioimpedance monitor.
|
baseline
|
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Fat free soft tissue
Time Frame: 3 months
|
Fat free mass is assessed using a bioimpedance monitor.
|
3 months
|
|
Fat free soft tissue
Time Frame: 6 months
|
Fat free mass is assessed using a bioimpedance monitor.
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Therese E Johnston, PT, PhD, MBA, Thomas Jefferson University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 164600
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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