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Clinical Trials in Switzerland / NCT07245706
Recruiting Not applicable

Shoulder Health After Rehabilitation and Performance Training

NCT07245706 · tracked via the Priya Life Science Switzerland tracker
Phase
Not applicable
Started
2026-07-16
Last updated
2026-07-23

Condition(s) studied

Spinal Cord InjuryNervous System DiseasesMusculoskeletal DiseasesInjury

Investigational drug(s) / intervention(s)

Strength training

Strength training: Individualized, home-based strength trainig consisting of 6 ecxercises that will be carried out twice a week for 12 weeks

Study summary

The goal of this study is to investigate the impact of a home-based shoulder strength training on the overall shoulder health in manual wheelchair users, and if the timepoint of such a training makes a difference. The study is focusing on persons with a spinal cord injury in the thoracic or lumbar region of the spine, that have only recently been injured and will soon be discharged from primary rehabilitation.

The shoulder training will take place either 3 or 12 months after discharge from primary rehabilitation and will be carried out twice a week for 12 weeks.

There are six measurements occurring every three months, which leads to an overall duration of 15 months. The measurements consist of:

* Questionnaires about independence in daily life, participation, quality of life and physical activity
* Assessment of shoulder strength, range of motion and function
* Measurement of the daily wheelchair use during one week via sensors that are fixed to the wheelchair and wrist
* one further questionnaire at the end of the measurement week about the occurrence of shoulder pain

Additionally, on four of the six measurement timepoints, a magnet resonance image (MRI) of the shoulder will be taken to assess the shoulder status (pathology, muscle volume and quality).

Though all these measurements the researchers can additionally assess the load of daily life on the shoulders, and how well this matches the preparation during the primary rehabilitation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Persons with a paraplegia below T2 * Manual wheelchair user * Age 18 - 70 years * At discharge from initial rehabilitation Exclusion Criteria: * Trauma or surgery of the shoulder with medical indication for immobilization of more than four weeks * Constant use of power assistance for the wheelchair * Any surgical implants that exclude the participant for MRI assessments of the shoulder * Inability to follow the study instructions, e.g., mental health problems, language problems, dementia, claustrophobia (for MRI) etc. * Persons with congenital conditions leading to SCI, SCI in the context of palliative care, neurodegenerative disorders, and Guillain-Barré syndrome * Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Swiss Paraplegic Research Nottwil Canton of Lucerne Recruiting

More Swiss Paraplegic Research, Nottwil trials in Switzerland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07245706 on ClinicalTrials.gov ↗ ← All trials in Switzerland