Preoperative optimisation of patient expectations through a video-based microintervention to improve treatment outcomes in orthopaedic surgery
Not Applicable
- Conditions
- Fracture of extremities, acute postoperative pain
- Registration Number
- DRKS00031516
- Lead Sponsor
- Philipps-Universität Marburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 126
Inclusion Criteria
elective surgery of the upper/lower extremities (fractures),
surgery scheduled within the next 3 days,
ability to consent to participate,
presence of a signed informed consent document,
sufficient command of the German language
Exclusion Criteria
younger than 18 years, not able to consent,
insufficient command of the German language,
emergency surgeries and tumour-related surgeries,
not wanting to participate
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity (11-point NRS), on postoperative days 1 and 7 (POD1, POD7)
- Secondary Outcome Measures
Name Time Method Pain-related disability (Pain Disability Index),<br>Health-related quality of life (SF-12),<br>Treatment satisfaction (11-point NRS)<br>Dose and amount of perioperatively consumed analgesics<br>State-Anxiety (STAI SKD),<br>Pain Catastrophising (PCS),<br>Items regarding expectations and perceived expectation violation (i.a. TEX-Q)<br>Participant feedback regarding video<br><br>Manipulation check after having received the intervention:<br>Surgical fear (SFQ),<br>State-Anxiety (STAI SKD)<br>Pain catastrophising (PCS),<br>Expectations (TEX-Q),<br>Perceived helpfulness regarding the intervention as well as degree to which participants feel adequately informed about the surgery (11-point NRS)