About this trial

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 criteria

Qualifiers

Persons with a paraplegia below T2

Manual wheelchair user

Age 18 - 70 years

At discharge from initial rehabilitation

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Strength training

Treatment groups

40 Participants
are divided into 2 treatment groups

Locations

1
Swiss Paraplegic Research6207, NottwilCanton of Lucerne, Switzerland

Sponsors and collaborators

Swiss Paraplegic Research, Nottwil

Lead sponsor

Swiss National Science Foundation

Collaborator