ACT for CABGAcceptance and Commitment Therapy for the Perioperative Period of Coronary Artery Bypass Graft Surgery: a Randomized Controlled Feasibility Trial
Acceptance and commitment therapy
Arterial Occlusive Diseases+9
+ Arteriosclerosis
+ Cardiovascular Diseases
Supportive Care Study
Summary
Study start date: February 12, 2024
Actual date on which the first participant was enrolled.This study focuses on helping patients who are undergoing coronary artery bypass graft (CABG) surgery, a procedure often needed when medications aren't enough to manage heart disease symptoms such as chest pain. Heart disease is a leading cause of death and carries a high economic cost. CABG can be lifesaving, but it also tends to increase inflammation and is associated with high levels of anxiety and depression around the time of surgery. These emotional challenges can worsen health outcomes and increase healthcare costs. The study aims to explore the use of Acceptance and Commitment Therapy (ACT), a type of psychological therapy, during the surgical period to help improve mental well-being and potentially improve physical health outcomes for these patients. Participants in this study are randomly assigned to one of two groups. One group receives a brief, two-session ACT therapy via telehealth, while the other group continues with their usual care without the additional therapy. The study measures the feasibility of delivering this therapy around the time of surgery and evaluates its preliminary effectiveness. Researchers look at various factors, including levels of anxiety, depression, overall well-being, and the quality of life related to heart health. They also check for changes in inflammation by measuring specific markers in the body. The findings could guide future, larger studies to support heart surgery patients better.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University of Iowa Hospitals and Clinics
Iowa City, United StatesOpen University of Iowa Hospitals and Clinics in Google Maps