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Behavioral Activation and Medication Optimization In Older Adults Undergoing Cardiac Procedures

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The Washington University

Status

Completed

Conditions

Cardiac Surgery
Older Adults
Depression
Anxiety

Treatments

Behavioral: Behavioral activation
Other: Medication optimzation
Other: Care as usual

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05575128
202209033
P50MH122351 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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 cardiac surgery (compared with usual care), while examining implementation outcomes.

Enrollment

102 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults ≥ 60 years
  • Scheduled major cardiac 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 CPMH feasibility study 202101103.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

102 participants in 2 patient groups

Behavioral activation and medication optimization
Experimental group
Description:
Behavioral activation (BA) will begin perioperatively and will span across 3 months postoperatively, with sessions approximately weekly or biweekly, depending on patient preference \& health condition. Medications will be reviewed by a team of interventionists to minimize brain-toxic medications and optimize doses of antidepressants and other mental health medications. In-hospital and after discharge, the interventionists' role will include coordinating with the care teams to ensure that medication changes that were introduced preoperatively are maintained.
Treatment:
Other: Medication optimzation
Behavioral: Behavioral activation
Control (treatment as usual)
Other group
Description:
Participants in control arm will continue care as usual. They will receive printed resources for supporting sleep hygiene, stress reduction, cognitive and mental health exercises, as well as community resources for older adults.
Treatment:
Other: Care as usual

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Caitlin Bess; Theresa Cordner, BS

Data sourced from clinicaltrials.gov

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