Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06174701

Building Resilience for Surgical Recovery

Led by The University of Texas Health Science Center, Houston · Updated on 2025-05-01

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center, Houston

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to test problem solving therapy (PST) in older adults who are undergoing major surgery. The main question it aims to answer is: What is the feasibility and acceptability of delivering PST to older surgical patients with depressive symptoms or report lacking social support in the pre-operative and post-operative setting?

CONDITIONS

Official Title

Building Resilience for Surgical Recovery

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 65 years of age or older on the day of surgery
  • Scheduled for major surgery with an expected hospital stay of 3 or more days, including orthopedic, thoracic, abdominal, or cardiac procedures
  • Have depressive symptoms with a Patient Health Questionnaire (PHQ-9) score of 5 or higher; if the score is 5-9, must have depressed mood or diminished activities as part of the symptoms
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment with 5 or more errors on the Short Portable Mental Status Questionnaire (SPMSQ)
  • Unable to read, speak, and understand English
  • Current alcohol or substance abuse indicated by scoring 2 or more on the CAGE questionnaire or using non-prescription drugs or substances
  • Life expectancy of 6 months or less

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of California, San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

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Research Team

J

Jude des Bordes, MBChB, MPH, DrPH, CPH

CONTACT

V

Victoria Tang, MD, MAS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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