CompletedNot Applicable

Perioperative Mental Health in Orthopedic Surgery

United States116 participantsStarted 2023-02-27

Plain-language summary

This Hybrid 1 Study will test the effectiveness of a bundled intervention comprised of behavioral activation and medication optimization in reducing symptoms of depression and anxiety in older adults undergoing Orthopedic surgery (compared with usual care), while examining implementation outcomes.

Who can participate

Age range60 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria: * Adults ≥ 60 years * Scheduled primary hip or primary knee arthroplasty procedure * PHQ-ADS ≥ 10, indicating clinically significant depression or anxiety symptoms Exclusion criteria: * Barrier to communication (Unable to read, speak, and understand English) * Severe cognitive impairment screened by the SBT (Short Blessed Test) \>10 * Acutely suicidal * Previous participation in this study or another CPMH study of the intervention bundle or its feasibility.

What they're measuring

PHQ-ADS (Patient Health Questionnaire Anxiety and Depression Scale)

Timeframe: Baseline and 3 months post-operatively

Trial details

NCT IDNCT05697835

SponsorWashington University School of Medicine

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-19

Results submitted2026-03-11

View on ClinicalTrials.gov More Orthopedic Surgery trials