Stress Management and Biomarkers of Risk in Cardiac Rehabilitation (ENHANCED)
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this study is to assess the extent to which combining exercise and stress management training (SMT) is more effective at improving biomarkers in vulnerable cardiac patients compared to exercise-based cardiac rehabilitation alone.
| Condition | Intervention |
|---|---|
|
Coronary Heart Disease |
Behavioral: SMT-enhanced Cardiac Rehabilitation Behavioral: Standard Cardiac Rehabilitation |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Enhancing Standard Cardiac Rehabilitation With Stress Management Training in Patients With Heart Disease |
- Stress and Biomarker Global Scores [ Time Frame: At 12 weeks ] [ Designated as safety issue: No ]
- Quality of life, death and cardiac hospitalizations. [ Time Frame: At 12 weeks and at 6 and 12 month follow up and annually for up to 4 years post-treatment ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 150 |
| Study Start Date: | September 2009 |
| Estimated Study Completion Date: | May 2014 |
| Estimated Primary Completion Date: | May 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: SMT-enhanced Cardiac Rehabilitation
Standard exercise-based cardiac rehabilitation with weekly stress management training for 12 weeks.
|
Behavioral: SMT-enhanced Cardiac Rehabilitation
Standard exercise-based cardiac rehabilitation, three times per week, enhanced with weekly stress management training for 12 weeks.
|
|
Active Comparator: Standard Cardiac Rehabilitation
Standard cardiac rehabilitation consisting of supervised exercise for 12 weeks.
|
Behavioral: Standard Cardiac Rehabilitation
Supervised exercise, three times per week, for 12 weeks.
|
Detailed Description:
Coronary heart disease (CHD) is the leading cause of death in the United States and in roughly half the cases its first clinical manifestations, myocardial infarction (MI) or sudden cardiac death (SCD), are fatal. There is considerable evidence that "stress" plays a significant and independent role in the occurrence of CHD and its complications. This evidence has provided the rationale for developing interventional strategies to reduce stress in susceptible individuals in order to modify the natural history of these clinical events. There are now promising data to suggest that stress management training (SMT) is one such approach, and that SMT can have beneficial effects on psychosocial and medical outcomes. However, many of the randomized clinical trials (RCTs) employing stress management approaches in CHD patients have had important methodological limitations and several of the larger RCTs have failed to demonstrate a benefit for SMT over usual care, raising questions about the value of SMT for patients with CHD. Reliance on "hard" clinical endpoints is problematic because studies require such large sample sizes that they are logistically difficult to conduct and are prohibitively expensive. The use of intermediate pathophysiologic endpoints that have been shown independently to be associated with increased risk represents a novel and exciting opportunity to examine the added value of SMT in exercise-based cardiac rehabilitation (CR) compared to CR without SMT on key biomarkers of risk in vulnerable CHD patients.
This 12-week study will enroll adults with stable CHD who are eligible for CR. Participants will be randomly assigned to either standard cardiac rehabilitation or standard cardiac rehabilitation enhanced with weekly SMT. Prior to randomization, medical screening, standardized psychosocial questionnaires, mental stress testing, assessment of diet and physical activity, and exercise testing will be conducted. Additional biomarkers of risk will be assessed through measures of flow-mediated vasodilation, inflammation, platelet function, stress hormones, baroreflex, and heart rate variability.
Participants assigned to CR alone will engage in supervised exercise routines 3 times per week. Participants will be encouraged to maintain consistent exercise duration and effort throughout each session. Participants assigned to CR enhanced with SMT will engage in standard exercise-based cardiac rehabilitation and also receive weekly group SMT. At the conclusion of the 12-week intervention, participants will return for repeat assessments of stress and biomarker measures. At 6 months, 12 months, and annually up to 4 years participants will be contacted for information regarding medical events and medication use.
Eligibility| Ages Eligible for Study: | 35 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Diagnosis of Coronary Heart Disease (CHD)
- Eligibility for Cardiac Rehabilitation (CR) in North Carolina
- Capacity to give informed consent and follow study procedures
Exclusion Criteria:
- Received heart transplant
- LVEF < 30%
- Labile ECG changes prior to testing
- Currently using a pacemaker
- Resting BP > 200/120 mm Hg
- Left main disease > 50%
- Unable to comply with assessment procedures
- Unwilling or unable to be randomized to treatment groups
- Primary diagnosis of the following psychiatric disorders: schizophrenia, dementia, current delirium, or other psychotic disorder
- Current alcohol or substance abuse disorder
- Acute suicide risk
- Actively undergoing ongoing psychiatric treatment
Contacts and Locations| Contact: James A. Blumenthal, PhD | 919-684-3828 | blume003@duke.edu |
| Contact: Stephanie K. Mabe, MS | 919-668-3555 | stephanie.mabe@duke.edu |
| United States, North Carolina | |
| University of North Carolina Hospitals - Meadowmont | Recruiting |
| Chapel Hill, North Carolina, United States, 27517 | |
| Contact: Alan Hinderliter, MD 919-216-3686 hinderli@med.unc.edu | |
| Sub-Investigator: Paula Miller, MD | |
| Duke University Medical Center - Center for Living | Recruiting |
| Durham, North Carolina, United States, 27710 | |
| Contact: James A. Blumenthal, PhD 919-684-3828 blume003@duke.edu | |
| Contact: Stephanie K. Mabe, MS 919-668-3555 stephanie.mabe@duke.edu | |
| Sub-Investigator: Andrew Sherwood, PhD | |
| Sub-Investigator: Michael A. Babyak, PhD | |
| Sub-Investigator: Lana Watkins, PhD | |
| Sub-Investigator: William E. Kraus, MD | |
| Principal Investigator: | James A. Blumenthal, PhD | Duke University |
| Principal Investigator: | Alan Hinderliter, MD | University of North Carolina, Chapel Hill |
More Information
Publications:
| Responsible Party: | Duke University |
| ClinicalTrials.gov Identifier: | NCT00981253 History of Changes |
| Other Study ID Numbers: | Pro00015896, R01HL093374-01A2, R01 HL093374-01A2 |
| Study First Received: | September 21, 2009 |
| Last Updated: | January 17, 2013 |
| Health Authority: | United States: Federal Government United States: Institutional Review Board |
Keywords provided by Duke University:
|
Stress Management Training Cardiac Rehabilitation Stress Depression |
Additional relevant MeSH terms:
|
Coronary Artery Disease Myocardial Ischemia Coronary Disease Heart Diseases |
Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases |
ClinicalTrials.gov processed this record on June 17, 2013