Shoulder pain, behavioural economics Musculoskeletal Diseases Shoulder lesions
Conditions
Interventions
The trial will involve randomisation of patients to three groups. Initially all participants complete the measures, as well as providing information regarding how much they think the treatment will co
Sponsors
Imperial College London (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Individuals undergoing primary arthroscopic shoulder decompression at the home institution 2. Informed consent in English
Exclusion criteria
Exclusion criteria: 1. Previous shoulder surgery on operative side 2. Unable to consent in English
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Health state (EQ5D) 2. Subjective wellbeing 3. Oxford shoulder score Measures will be taken at enrolment, on the morning of surgery (typically 2-4 weeks after enrolment) and then again at 6 weeks following surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction measures at 6 weeks post-surgery | — |
Countries
United Kingdom
Outcome results
None listed