Prospective Abuse and Intimate Partner Violence Surgical Evaluation (PRAISE-2) Protocol
Completed
- Conditions
- Musculoskeletal injury10017322
- Registration Number
- NL-OMON43260
- Lead Sponsor
- McMaster University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1) Adult females (at least 18 years of age)
2) Patients presenting within 6 weeks of their musculoskeletal injury
3) Patients presenting with a fracture or dislocation which is being managed with either surgical or non-surgical treatment
Exclusion Criteria
1) Unwilling to or unable to provide consent
2) Unable to complete the study questionnaires in a private location, due to safety and confidentiality
3) Unwilling or unable to follow the study protocol or their attending surgeon has concerns about their ability or willingness to follow study protocols
4) Does not speak and write in Dutch
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome of the pilot study will be a composite measure of<br /><br>feasibility. This will include:<br /><br>1) Recruitment (number of patients recruited at each site during a 12 month<br /><br>period)<br /><br>2) Protocol adherence (application of eligibility criteria)<br /><br>3) Follow-up (proportion of included patients followed at 12 months)<br /><br>4) Data quality (the proportion of case report forms, including patient<br /><br>questionnaires completed at 12 months)</p><br>
- Secondary Outcome Measures
Name Time Method