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

NCT06775925 · Swiss Paraplegic Research, Nottwil · Updated 8 July 2026

What is being tested
Unilateral robot-assisted therapy (RT); Unilateral conventional occupational therapy (OT)
For
Cervical Spinal Cord Injury
Kind of study
Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
Who can join
Ages 18 years and older. About 40 people. The full rules are on the registry page.
Where
Switzerland
When
Starts or started 1 Feb 2025, ends Dec 2027. Registered 15 Jan 2025.
Results
None posted yet.

In the researchers' words

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)
ClinicalTrials.gov, NCT06775925

Sites

  • Swiss Paraplegic CentreNottwil, Canton of Lucerne, Switzerland