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The Effects of Eccentric Compared to Standard Strength Training in Primary Spinal Cord Injury Rehabilitation

Study acronym: KREHA3
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Jul 2028 → Dec 2028
See other at-risk trials from Swiss Paraplegic Research, Nottwil

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Start date: Jul 2026 to Dec 2026
    • Primary and study completion pushed from Jul 2028 to Dec 2028
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 7 of 7 entries
  2. Notable Start date: Mar 1, 2026 to Jul 2026
    • Primary and study completion dates: Mar 1, 2028 to Jul 2028
    v4
  3. Notable Primary and study completion dates: Jul 1, 2027 to Mar 1, 2028
    • Start date: Dec 1, 2025 to Mar 1, 2026
    v3
  4. Notable Start date: Jul 1, 2025 to Dec 1, 2025v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to assess the effects of eccentric arm-crank (KREHA) training compared to standard clinical routine strength (STAN) training in individuals undergoing primary spinal cord injury (SCI) rehabilitation. The main questions this trail aims to answer are: * what are the effects of the training on upper body strength, aerobic performance, muscle volume, functional independence, and health-related quality of life? * is the KREHA training feasible to implement into the rehabilitation routine? Participants will: * perform either 20 KREHA sessions or 20 STAN sessions within 12 weeks * perform a test battery to collect data on training effects before (pretest) and after (posttest) the study intervention
Trial Details
NCT Number NCT06905470
Lead Sponsor Swiss Paraplegic Research, Nottwil
Conditions
(from sponsor)
Spinal Cord Injury
Related terms Spinal Cord Injuries
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov