Psychological Factors and Pain in Orthopedic Surgery Patients
Recruiting
Observational Study
Orthopedic Surgical Procedures
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Observational
Participants needed
170 (estimated)
Sponsor
Jagiellonian University · Other
Who this trial is looking for
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The goal of this observational study is to verify the association of previously underexplored psychological variables on postoperative pain experience and its progression over time in patients undergoing emergency and elective orthopedic surgeries, including both sexes (age range: 18-65). The main questions it aims to answer are:
1. Do psychological factors such as dysfunctional personality trait…
The goal of this observational study is to verify the association of previously underexplored psychological variables on postoperative pain experience and its progression over time in patients undergoing emergency and elective orthopedic surgeries, including both sexes (age range: 18-65). The main questions it aims to answer are:
1. Do psychological factors such as dysfunctional personality traits and emotional regulation explain the experience of pain after surgery and after six months?
2. Does the experience of the body mediate the relationship between dysfunctional personality traits and the experience of pain after surgery and after six months?
3. Does the experience of pain differ between patients who underwent emergency and elective orthopedic surgery (after surgery and after six months)?
Researchers will compare the pain experience of patients undergoing emergency orthopedic surgery to those undergoing elective orthopedic surgery to see if there are significant differences in pain outcomes and recovery trajectories.
Participants will:
* complete psychological questionnairs to evaluate dysfunctional personality traits, emotional regulation, and body image;
* report their subjective pain level and provide information on their coping strategies for managing pain and information about pain interference in everyday functioning;
* engage in follow-up evaluation (6 months after the surgery) to assess the impact of pain on their daily activities and rehabilitation progress and complete some of the questionnaires again.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* age: participants aged 18 years or older;
* surgical procedures: individuals scheduled to undergo either emergency or elective orthopedic surgeries, including but not limited to joint replacements (e.g., hip or knee arthroplasty) and fracture repairs;
* time after operation: u…
Inclusion Criteria:
* age: participants aged 18 years or older;
* surgical procedures: individuals scheduled to undergo either emergency or elective orthopedic surgeries, including but not limited to joint replacements (e.g., hip or knee arthroplasty) and fracture repairs;
* time after operation: undergoing orthopedic surgery up to 72 hours before the psychological examination;
* informed consent: ability to provide informed consent and willingness to participate in the study;
* language proficiency: proficiency in the language of the questionnaires used in the study (Polish).
Exclusion Criteria:
* psychiatric disorders: diagnosed psychiatric disorders (e.g., severe depression, anxiety disorders) that are not managed or stable.
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