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NCT05697835
Perioperative Mental Health in Orthopedic Surgery
Conditions: Orthopedic Surgery, Older Adults, Depression, Anxiety
Sex: All
Ages: 60 Years – N/A
Phase: NA
Enrollment: 100
Sponsor: Washington University School of Medicine
Location: United States
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.
Eligibility Criteria
Inclusion criteria:Adults ≥ 60 yearsScheduled primary hip or primary knee arthroplasty procedurePHQ-ADS ≥ 10, indicating clinically significant depression or anxiety symptomsExclusion criteria:Barrier to communication (Unable to read, speak, and understand English)Severe cognitive impairment screened by the SBT (Short Blessed Test) >10Acutely suicidalPrevious participation in this study or another CPMH study of the intervention bundle or its feasibility.
Source: ClinicalTrials.gov (NCT05697835). StuddyBuddy aggregates publicly available trial information.
