Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID06207318

Acceptance and Commitment Therapy for the Perioperative Period of Coronary Artery Bypass Graft Surgery: a Randomized Controlled Feasibility Trial

Led by University of Iowa · Updated on 2025-08-08

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Heart disease is the leading cause of death worldwide, contributing to 16% of global fatalities and imposing a significant economic burden, especially as the population ages. Some patients with heart disease experience symptoms not relieved by medications and require coronary artery bypass graft (CABG) surgery. Although CABG can improve chest pain and has life-prolonging potential, it may increase inflammation and is often accompanied by high levels of anxiety and depression around the time of surgery, which can affect health outcomes and quality of life. This trial is a randomized controlled feasibility study comparing a brief, two-session telehealth Acceptance and Commitment Therapy (ACT) intervention to treatment as usual for patients undergoing CABG surgery. The ACT intervention focuses on psychological flexibility through core processes such as being present, opening up, and doing what matters, and includes workbooks and mindfulness audio exercises. The control group receives usual preoperative care, including appointments with surgeons and nurse practitioners and educational workbooks about hospital orientation and lifestyle factors. Participants will be assessed on measures of anxiety, depression, psychological flexibility, well-being, cardiovascular health-related quality of life, and inflammation markers before surgery and at 8 weeks after. Researchers will monitor feasibility factors like participant satisfaction, adherence, enrollment, intervention delivery, and retention. The study aims to evaluate both the feasibility and preliminary effects of ACT during the perioperative period for CABG patients, helping guide future larger trials.

CONDITIONS

Brief Title

Acceptance and Commitment Therapy for Patients Undergoing Coronary Artery Bypass Graft Surgery

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Admission to the Heart and Vascular Center at University of Iowa Hospitals and Clinics for urgent or elective coronary artery bypass graft (CABG) surgery
  • Access to a personal phone or device with video or audio capabilities
  • Ability to provide informed consent
  • English fluency
Not Eligible

You will not qualify if you...

  • Life-threatening comorbid (noncardiac) medical condition(s)
  • Active suicidal ideation or intent
  • Psychotropic medication use lasting less than four weeks
  • Inability to provide informed consent and comply with study procedures
  • Undergoing repeat revascularization

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 8 weeks

Participants receive two sessions of Acceptance and Commitment Therapy (ACT) focusing on psychological flexibility, personal values, and health-related goals around surgery. Sessions last 60-90 minutes each, with additional workbook and mindfulness exercises provided. Control participants receive treatment as usual including preoperative appointments and educational materials.

2 therapy sessions and 1 preoperative appointment

Follow-up

Duration - Up to 8 weeks

Participants complete questionnaires and assessments to evaluate satisfaction, adherence, mental health, quality of life, and biomarkers up to 8 weeks after intervention.

1 to 2 follow-up visits

Trial Site Locations

Total: 1 location

1

University of Iowa Hospitals and Clinics

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

S

Sara J Diesel, MA

M

Mark Vander Weg, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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