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Study identifier: NCT06775925 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Robot-assisted vs. Conventional Occupational Therapy of the Upper Limb in Individuals With Cervical Spinal Cord Injury

Condition: Cervical Spinal Cord Injury  ·  Sponsor: Swiss Paraplegic Research, Nottwil

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn the effects of robot-assisted therapy using the ArmeoSpring on upper limb function compared to conventional occupational therpay in individuals with cervical spinal cord injury (cSCI). The main questions it aims to answer are: \- Which of the two forms of therapy, robot-assisted therapy or conventional occupational therapy, is more effective in terms of improving arm and hand function? The study is designed as a cross-over trial, which means that each participant will receive both therapy forms consecutively, whereas the order is assigned randomly (either robot-assisted therapy first and then occupational therapy, or vice versa). In addition to their clinical routine therapy , participants will: * complete a baseline assessment * practice one therapy form (either robot-assisted or occupational therapy) with one arm for 6 weeks (3 x 30 min per week) * complete a intermediate assessment * practice the other therapy form (either occupational or robot-assisted therapy) with one arm for 6 weeks (3 x 30 min per week) * complete a post assessment * complete a follow-up assessment (if the post assessment was completed prior to 150 days post-injury)

This description comes directly from the study's public registry record.

Talk to the study team

Mario Widmer, Dr. sc. ETH  ·  0041 41 939 51 97  ·  mario.widmer@paraplegie.ch

Chantal Wunderlin  ·  0041 41 939 66 15  ·  chantal.wunderlin@paraplegie.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Swiss Paraplegic CentreNottwil, Canton of Lucerne, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT06775925