Acute rehabilitation following traumatic anterior shoulder dislocatio

Not Applicable

Completed

• Conditions: Shoulder dislocation; Injury, Occupational Diseases, Poisoning

• Registration Number: ISRCTN63184243
• Lead Sponsor: niversity Hospitals Coventry and Warwickshire NHS Trust

Brief Summary

2020 Protocol article in https://pubmed.ncbi.nlm.nih.gov/33444204/ protocol (added 18/01/2021) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34607077/ intervention development (added 05/10/2021) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/38233068/ (added 18/01/2024)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-09-07
• Study Completion: 2022-11-30
• Last Update Posted: 29 January 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 482

Inclusion Criteria

1. Provision of written informed consent
2. Aged 18 years or over
3. Patients have a primary traumatic acute shoulder dislocation, confirmed by radiology

Exclusion Criteria

1. Bilateral shoulder dislocation
2. Having first-line surgical treatment (Indications include a displaced greater tuberosity fracture for example)
3. Cannot receive first session of physiotherapy within 6 weeks of injury
4. In the opinion of the assessing clinician there is a neurovascular complication associated with TASD
5. Unable to adhere to trial procedures or complete questionnaires; for example, a history of permanent cognitive impairment
6. Previous randomisation in the present trial

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Oxford Shoulder Instability Score (OSIS): The OSIS is a self-completed outcome measure containing 12 questions (0-4 points each), with possible scores from 0 (best function) to 48 (worst function) (8, 11). These questions relate to activities of daily living particularly relevant to patients exhibiting shoulder instability. The OSIS has been specifically designed to assess outcome of therapy (both surgical and non-surgical) by measuring activities of daily living and pain of patients exhibiting shoulder instability. Measured at 6 months after injury.