Spinal Cord Injuries Clinical Trial
— KREHA-ParAthOfficial title:
Strength Training With Eccentric Arm-cranking in Para-athletes
NCT number | NCT05777941 |
Other study ID # | 2022-06 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 1, 2022 |
Est. completion date | May 30, 2024 |
The new training device, the eccentric arm-crank, will be examined for its training effects in athletes with a spinal cord injury (SCI) by this project. That the training device can be used in patients with paraplegia in the future, the so-called "testing of the applicability of this concept" will be carried out during this study. Fourteen volunteer, healthy athletes with SCI are first tested for their upper body performance, followed by a training phase over 20 trainings and at the end the performance data is collected again. The training intensity and duration is continuously increased during the training phase.
Status | Recruiting |
Enrollment | 14 |
Est. completion date | May 30, 2024 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - male or female with traumatic or disease-related SCI - age between 18 and 50 years - experience in strength training - Squad status or at least 4h per week training - Biceps/triceps function - healthy(study physician) - adequately informed and confirmed per signature Exclusion Criteria: - findings during anamnesis of study physician - pregnancy |
Country | Name | City | State |
---|---|---|---|
Switzerland | Swiss Paraplegic Centre | Nottwil | Lucerne |
Lead Sponsor | Collaborator |
---|---|
Swiss Paraplegic Research, Nottwil |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Upper body Performance | Peak Power - maximal reached power, generated during the 30sec Wingate arm-crank test | through study completion, an average of 20 weeks | |
Secondary | Endurance Oxygen consumption | VO2peak [ml/min/kg] - Basic Endurance test (Ergospirometry, arm-crank) | through study completion, an average of 20 weeks | |
Secondary | Maximal Workload | Wmax [W] - Basic Endurance test (Ergospirometry, arm-crank) | through study completion, an average of 20 weeks | |
Secondary | Upper body Mean Power | Mean Power [W] - Wingate Test (arm-crank) | through study completion, an average of 20 weeks | |
Secondary | Upper body Power - Time to Peak | Time to Peak [s] - Wingate Test (arm-crank) | through study completion, an average of 20 weeks | |
Secondary | Upper body Fatigue Index | Fatigue Index [%]- Wingate Test (arm-crank) | through study completion, an average of 20 weeks | |
Secondary | Upper body Fatigue Slope | Fatigue Slope [W/s] - Wingate Test (arm-crank) | through study completion, an average of 20 weeks | |
Secondary | 1RM bench press | One Repetition Maximum (1RM) [kg]- bench press | through study completion, an average of 20 weeks | |
Secondary | Grip Strength | Maximal Force that can be generated by pressing hand towards a fist [N] | through study completion, an average of 20 weeks | |
Secondary | Upper Arm Circumference | Circumference of the upper arm is measured with measuring tape | through study completion, an average of 20 weeks | |
Secondary | Lower Arm Circumference | Circumference of the lower arm is measured with measuring tape | through study completion, an average of 20 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT06321172 -
Muscle and Bone Changes After 6 Months of FES Cycling
|
N/A | |
Completed |
NCT03457714 -
Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
|
||
Recruiting |
NCT05484557 -
Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury
|
N/A | |
Suspended |
NCT05542238 -
The Effect of Acute Exercise on Cardiac Autonomic, Cerebrovascular, and Cognitive Function in Spinal Cord Injury
|
N/A | |
Recruiting |
NCT05503316 -
The Roll of Balance Confidence in Gait Rehabilitation in Persons With a Lesion of the Central Nervous System
|
N/A | |
Not yet recruiting |
NCT05506657 -
Early Intervention to Promote Return to Work for People With Spinal Cord Injury
|
N/A | |
Recruiting |
NCT03680872 -
Restoring Motor and Sensory Hand Function in Tetraplegia Using a Neural Bypass System
|
N/A | |
Recruiting |
NCT04105114 -
Transformation of Paralysis to Stepping
|
Early Phase 1 | |
Completed |
NCT04221373 -
Exoskeletal-Assisted Walking in SCI Acute Inpatient Rehabilitation
|
N/A | |
Completed |
NCT00116337 -
Spinal Cord Stimulation to Restore Cough
|
N/A | |
Completed |
NCT03898700 -
Coaching for Caregivers of Children With Spinal Cord Injury
|
N/A | |
Recruiting |
NCT04883463 -
Neuromodulation to Improve Respiratory Function in Cervical Spinal Cord Injury
|
N/A | |
Active, not recruiting |
NCT04881565 -
Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES)
|
N/A | |
Completed |
NCT04864262 -
Photovoice for Spinal Cord Injury to Prevent Falls
|
N/A | |
Recruiting |
NCT04007380 -
Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI
|
N/A | |
Active, not recruiting |
NCT04544761 -
Resilience in Persons Following Spinal Cord Injury
|
||
Terminated |
NCT03170557 -
Randomized Comparative Trial for Persistent Pain in Spinal Cord Injury: Acupuncture vs Aspecific Needle Skin Stimulation
|
N/A | |
Completed |
NCT03220451 -
Use of Adhesive Elastic Taping for the Therapy of Medium/Severe Pressure Ulcers in Spinal Cord Injured Patients
|
N/A | |
Recruiting |
NCT04811235 -
Optical Monitoring With Near-Infrared Spectroscopy for Spinal Cord Injury Trial
|
N/A | |
Recruiting |
NCT04736849 -
Epidural and Dorsal Root Stimulation in Humans With Spinal Cord Injury
|
N/A |