Psychological Distress and Outcomes in Hip Preservation Patients

NCT ID: NCT01550263

Last Updated: 2023-02-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

217 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-01-31

Study Completion Date

2022-11-30

Brief Summary

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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

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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.

Conditions

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Psychological Distress

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1. Primary presenting complaint of hip pain
2. 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

1. Unable to complete the DRAM questionnaire
2. Patients who do not undergo surgery
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Utah

OTHER

Sponsor Role lead

Responsible Party

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Stephen Aoki

M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Stephen K Aoki, MD

Role: PRINCIPAL_INVESTIGATOR

Orthopaedic Center

Locations

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Orthopaedic Center

Salt Lake City, Utah, United States

Site Status

Countries

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United States

Other Identifiers

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48948

Identifier Type: -

Identifier Source: org_study_id

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