Chronic, unilateral shoulder pain in adults
Conditions
Interventions
Group 1: All participants undergo the same study procedure, which includes a clinical examination, wearing sensors for two weeks, daily questionnaires and a final visit.
Sponsors
Universitätsklinikum Heidelberg, vertreten durch PD Dr. med. Benjamin Panzram
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: unilateral shoulder pain that has been present for at least three months, sufficient mobility of the shoulder to perform everyday movements and the ability to give informed consent.
Exclusion criteria
Exclusion criteria: Pregnant women, patients with an acute shoulder injury or shoulder surgery within the last three months, with acute inflammatory diseases or infections in the shoulder area or adjacent structures, with a pacemaker or ICD, with known underlying neurological diseases with sensorimotor deficits, people with mental or cognitive impairments and patients who do not agree to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between clinically/subjectively recorded movement parameters and inertial sensor-based everyday movement data of the affected shoulder. | — |
Secondary
| Measure | Time frame |
|---|---|
| Identification of typical movement-pain patterns, as well as assessment of the wearing comfort and suitability of the sensors for everyday use by the participants. | — |
Countries
Germany
Contacts
Public ContactBenjamin Panzram
Orthopädische Universitätsklinik Heidelberg
Outcome results
None listed