Spinal Cord Injury Clinical Trial
Official title:
Using Musculoskeletal Models to Assess FES Rowing for Skeletal Health After SCI
Following a complete spinal cord injury (SCI), individuals experience progressive bone loss, especially in the legs, with up to 70% of persons with SCI sustaining a fracture at some point during their lifetime. Fractures following SCI are costly to treat and more than half of patients experience a medical complication, requiring extended hospitalization, resulting in a substantial impact on their quality of life. To reduce the incidence of fractures, more effective rehabilitation strategies to prevent bone loss are needed. The goal of this research is to determine if bone health can be preserved using an indoor rowing exercise program in which the leg muscles are electrically stimulated using several, small surface electrode pads that are placed on the skin on the front and back thigh muscles. An encouraging case study has recently shown remarkable bone preservation in one individual with SCI who participated in an electrical stimulation rowing program, however, whether other individuals with SCI can achieve the same benefit is currently unknown.
In this study the investigators expect to enroll a total of 10 participants with SCI. Five
participants will be assigned to a Standard-of-Care (control) group and five participants
will be assigned to an FES-rowing intervention group. Group assignment will be partly based
on the preference of each potential participant and their willingness to make the necessary
time commitment required for participation in a given group, with the added goal, to the
extent possible, of matching the two groups for age, gender and time since injury. Only those
individuals who have a strong desire to participate in a regular exercise program and who
express a willingness to travel to VA Palo Alto the necessary number of times per week to
perform FES-rowing will be potential candidates for inclusion in the rowing group.
Bone density measurements for both the Standard-of-Care group and the FES-rowing group will
be performed using Dual energy X-ray Absorptiometry (DXA) and peripheral Quantitative
Computed Tomography (pQCT). The Standard-of-Care group will undergo no other research
procedures.
The muscle conditioning program is accomplished through electrical stimulation of the
quadriceps and hamstring muscles using a 4-channel electrical stimulator that applies
stimulation using surface electrodes adhered using gel to the skin overlying the quadriceps
and hamstrings muscles. The muscle strengthening initially takes place three times per week,
sixty minutes per session, progressing up to five sessions per week, for approximately 8
weeks. The muscle strengthening program ensures that subjects have sufficient muscle strength
and endurance before they embark on the rowing program. Following the 8-week muscle
strengthening program, subjects will begin FES-rowing, with three sessions per week, thirty
minutes per session for the following 28 weeks. In the FES-rowing group, the investigators
will measure isometric knee extension strength at the start of week 0, and at the end of
weeks 12, 24 and 36.
For the rowing group, the investigators will capture 3D kinetics and kinematics in the motion
capture laboratory during FES-rowing at the end of weeks 12, 24 and 36. Kinematics during
rowing will be collected from fifty passive retro-reflective markers that will be placed on
each participant to capture the position and orientation of the 12 interconnected body
segments used to represent each subject.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02574572 -
Autologous Mesenchymal Stem Cells Transplantation in Cervical Chronic and Complete Spinal Cord Injury
|
Phase 1 | |
Recruiting |
NCT05941819 -
ARC Therapy to Restore Hemodynamic Stability and Trunk Control in People With Spinal Cord Injury
|
N/A | |
Completed |
NCT05265377 -
Safety and Usability of the STELO Exoskeleton in People With Acquired Brain Injury and Spinal Cord Injury
|
N/A | |
Recruiting |
NCT02331979 -
Improving Bladder Function in SCI by Neuromodulation
|
N/A | |
Completed |
NCT02777281 -
Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
|
N/A | |
Recruiting |
NCT02978638 -
Electrical Stimulation for Continence After Spinal Cord Injury
|
N/A | |
Completed |
NCT02262234 -
Education Interventions for Self-Management of Pain Post-SCI: A Pilot Study
|
Phase 1/Phase 2 | |
Withdrawn |
NCT02237547 -
Safety and Feasibility Study of Cell Therapy in Treatment of Spinal Cord Injury
|
Phase 1/Phase 2 | |
Completed |
NCT02161913 -
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
|
N/A | |
Terminated |
NCT02080039 -
Electrical Stimulation of Denervated Muscles After Spinal Cord Injury
|
N/A | |
Completed |
NCT01642901 -
Zoledronic Acid in Acute Spinal Cord Injury
|
Phase 3 | |
Completed |
NCT01884662 -
Virtual Walking for Neuropathic Pain in Spinal Cord Injury
|
N/A | |
Completed |
NCT01471613 -
Lithium, Cord Blood Cells and the Combination in the Treatment of Acute & Sub-acute Spinal Cord Injury
|
Phase 1/Phase 2 | |
Terminated |
NCT01433159 -
Comparison of HP011-101 to Standard Care for Stage I-II Pressure Ulcers in Subjects With Spinal Cord Injury
|
Phase 2 | |
Completed |
NCT02149511 -
Longitudinal Morphometric Changes Following SCI
|
||
Completed |
NCT01467817 -
Obesity/Overweight in Persons With Early and Chronic Spinal Cord Injury (SCI)
|
N/A | |
Terminated |
NCT01005615 -
Patterned Functional Electrical Stimulation (FES) Ergometry of Arm and Shoulder in Individuals With Spinal Cord Injury
|
Phase 1/Phase 2 | |
Completed |
NCT01025609 -
Dietary Patterns and Cardiovascular (CVD) Risk in Spinal Cord Injury (SCI) Factors In Individuals With Chronic Spinal Cord Injury
|
||
Completed |
NCT01086930 -
Early Intensive Hand Rehabilitation After Spinal Cord Injury
|
Phase 3 | |
Completed |
NCT00663663 -
Telephone Intervention for Pain Study (TIPS)
|
N/A |