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Clinical Trials/NCT01550263
NCT01550263
Completed
N/A

Pre-Operative Psychological Distress and Post-Operative Outcomes in Hip Preservation Patients

University of Utah1 site in 1 country217 target enrollmentJanuary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Psychological Distress
Sponsor
University of Utah
Enrollment
217
Locations
1
Primary Endpoint
Distress and Risk Assessment Method (DRAM) questionaire
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is an investigatory study to determine whether high levels of pre-operative psychological distress predict worse outcomes after hip preservation. This is a low risk study and does not alter the treatment or course of care for patients undergoing this procedure

Detailed Description

The correlation between increasing psychological distress and worsening surgical outcomes has been extensively documented in patients undergoing spine surgery. However, we have no reason to believe that patients with hip pathology are uniquely exempt from the influence of psychosocial factors. To our knowledge, no study has been done to evaluate the effect of pre-operative psychological distress on outcomes after hip preservation surgery. We therefore propose to use the DRAM to measure pre-operative distress in patients undergoing open or arthroscopic hip preservation surgery and to compare these pre-operative distress scores with post-operative outcomes. We hope the information we gain will allow clinicians to comprehensively evaluate the patient with hip pain and to make more informed choices about operative treatment.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
November 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stephen Aoki

M.D.

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Primary presenting complaint of hip pain
  • Hip arthroscopy, surgical dislocation and debridement, and/or periacetabular osteotomy performed by Dr. Aoki or Dr. Peters for hip pathology diagnosed by history, clinical examination and/or imaging

Exclusion Criteria

  • Unable to complete the DRAM questionnaire
  • Patients who do not undergo surgery

Outcomes

Primary Outcomes

Distress and Risk Assessment Method (DRAM) questionaire

Time Frame: 1 year

Distress and Risk Assessment Method (DRAM) questionaire to screen for psychological distress. The instrument defines four categories based on patients responses: Type N (normal; lower scores, no evidence of distress); Type R (at risk; higher scores, primarily in symptoms of depression); Type DD (distressed-depressive; higher scores on all variables, but very high on depressive symptomatology); and Type DS (distressed-somatic; higher scores on all variables, but very high on somatic awareness).

Study Sites (1)

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