Eccentric arm-cranking strength training for para-athletes
Strength Training With Eccentric Arm-cranking in Para-athletes
This study tests a new arm-cranking training device to see if it can help athletes with spinal cord injuries get stronger and improve their performance.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 14 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | All |
| Sponsor | Swiss Paraplegic Research, Nottwil Research network |
| Locations | 1 site (Nottwil, Lucerne) |
| Trial ID | NCT05777941 on ClinicalTrials.gov |
What this trial studies
This study examines the effects of a new training device, the eccentric arm-crank, on athletes with spinal cord injuries (SCI). Fourteen healthy volunteers with SCI will undergo performance testing followed by a training phase consisting of 20 sessions over a maximum of twelve weeks. The training intensity will be progressively increased, and performance data will be collected before and after the training phase to assess improvements. The study aims to evaluate the applicability of this training concept for individuals with paraplegia.
Who should consider this trial
Good fit: Ideal candidates are males or females aged 18 to 50 with traumatic or disease-related spinal cord injuries who have experience in strength training.
Not a fit: Patients who are pregnant or have contraindications identified by the study physician may not benefit from this study.
Why it matters
Potential benefit: If successful, this training could enhance upper body strength and performance in para-athletes with spinal cord injuries.
How similar studies have performed: While this approach is innovative, similar studies have shown promise in strength training for individuals with disabilities, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Nottwil, Lucerne
- Swiss Paraplegic Centre — Nottwil, Lucerne, Switzerland (Recruiting)
Study contacts
- Principal investigator: Fabian Ammann, MSc — Spz
- Study coordinator: Fabian Ammann, MSc
- Email: fabian.ammann@sportmedizin-nottwil.ch
- Phone: +41419396624
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.