search
Back to results

Optimizing Expectations in Cardiac Surgery Patients

Primary Purpose

Coronary Artery Bypass Graft Surgery (CABG), Patients' Expectations, Coronary Heart Disease

Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Expectation Manipulation Intervention
Supportive Therapy
Sponsored by
Philipps University Marburg Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Bypass Graft Surgery (CABG) focused on measuring Coronary Artery Bypass Graft Surgery (CABG), Patients' Expectations, Coronary Heart Disease, Illness Perception Intervention, Randomized Controlled Trial

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients scheduled on the elective waiting list for first time coronary artery bypass graft surgery wiht the use of heart-lung-apparatus at the Department of Cardiovascular Surgery, Medical School, University of Marburg
  • Sufficient knowledge of German language
  • Ability to give informed consent

Exclusion Criteria:

  • Emergency surgery
  • Presence of a serious comorbid psychiatric condition
  • Presence of a life threatening comorbid medical condition
  • Current participation in other research

Sites / Locations

  • Philipps University of Marburg

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Experimental

Arm Label

Standard Medical Care

Attention Control Group

Expectation Manipulation Intervention

Arm Description

Patients receive standard treatment protocol for Coronary Artery Bypass Graft Surgery

In addition to standard medical care patients receive a comparable amount of therapist´s attention (common and unspecific factors = supportive therapy) to the intervention group, without targeting patients' expectations.

In addition to standard medical care patients' expectations prior to surgery are targeted in a brief psycho-educational intervention.

Outcomes

Primary Outcome Measures

Disability 6 months after surgery, controlled for baseline disability (Pain Disability Index; PDI)

Secondary Outcome Measures

Change in Patients' Expectations from Baseline/Pre-Intervention (expected average of 10 days before surgery) to hospital admission/Post-Intervention (expected average of 1 day before surgery).
Prospective Illness Perception 6 months after surgery (Expected Illness Perception Questionnaire; IPQ-E), Positive Health Expectation Scale (PHES), Expected Disability (PDI-E)
Change in Cardiac Anxiety (Cardiac Anxiety Questionnaire; CAQ) from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Change in Physical Activity (International Physical Activity Questionnaire; IPAQ) from Baseline (an expected average of 10 days before surgery) to 6 months after surgery.
Change in Health Related Quality of Life (SF-12) from Baseline (expected average of 10 days before surgery) to 6 months after surgery.
Change in physical symptoms, subjective side effects and post-surgery complaints (Generic Assessment of Side Effects Scale; GASE-P)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Change in Hospital Anxiety and Depression Scale (HADS)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Change in Beliefs about Medications (Beliefs about Medications Questionaire; BMQ)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Change in Working ability from Baseline (expected average of 10 days before surgery) to 6 months after surgery.
Satisfaction wiht the intervention.
Cardiothoracic surgeons' rating of the surgery success
Additional treatments during follow-up
Additional Treatments, rehospitalizations, cardiac sport groups, rehabilitations programms, etc.
Blinded Expert Rating of medical and psychological status at follow-up
Change in Sleep Quality from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Change in neuroendocrine and immunological measures from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
cortisol, inflammatory processes, catecholamines
Patient Pre-/Peri-/Postoperative Health Status retrospectively collected from patient file
From Patient file: Left ventricular ejection fraction (EF), Body Mass Index, Blood pressure, Smoking status, Cardiac Operative Risk (EuroSCORE), New York Heart Association classification (NYHA), Canadian Cardiovascular Society grading of angina pectoris (CCS), Number of diseased coronary vessels, Previous myocardial infarctions, extra-cardiac arteriopathy, non-cardiac comorbidities, surgery procedure, surgery complications and in-hospital post surgery complications, time spent on the intensive care unit, inpatient days until discharge
Patients' experience with prior surgeries
Rating of experience with own prior surgeries. Rating of experience with surgeries of close others.
Enriched Social Support Inventory
Occurrence of major life events since surgery
Change in Patients' Illness Perception (Brief Illness Perception Questionnaire (B-IPQ) from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Satisfaction with the intervention

Full Information

First Posted
July 25, 2011
Last Updated
February 2, 2016
Sponsor
Philipps University Marburg Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT01407055
Brief Title
Optimizing Expectations in Cardiac Surgery Patients
Official Title
Clinical Applications of Placebo Research: Optimizing Expectation Effects in Cardiac Surgery Patients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Philipps University Marburg Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the potential benefit of targeting patients' expectations before coronary artery bypass graft surgery through a brief psychoeducational intervention.
Detailed Description
Coronary artery bypass graft surgery (CABG) is an extremely invasive medical intervention.It is postulated that even under these conditions, treatment outcome is substantially determined by non-specific effects, e.g. patient's expectation. Targeting patients' expectations at an early stage might have potential to optimize outcomes after cardiac surgery. The purpose of this research project is to optimize patients' outcome expectations before undergoing cardiac surgery through a brief psycho-educational program. Using a randomized controlled design, 180 patients who are scheduled to undergo elective CABG are randomly assigned either to standard medical information alone, or to an additional expectation manipulation intervention (EMI) during the two weeks before surgery, or to an attention-control group ("supportive therapy"). The main goal is to enhance positive expectations (surgery 'non-specific effects') about favorable outcome through EMI, about coping abilities to deal with adverse events, and to reduce negative expectations and misconceptions. Assessment takes place before and after EMI, 10 days after surgery and 6 months later; same assessment points are used for the 2 control conditions. Primary outcome is disability, which has been shown to be strongly determined by patient's expectation in previous studies. Moreover, psychological and biological predictors and mediators of treatment success are analyzed. A positive result for this expectation intervention would have major implications for clinical practice. In order to optimize treatment outcome, it is not only necessary to improve the treatment-specific procedures (e.g., cardiac surgery) but also to address non-specific factors such as patients' expectations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Bypass Graft Surgery (CABG), Patients' Expectations, Coronary Heart Disease
Keywords
Coronary Artery Bypass Graft Surgery (CABG), Patients' Expectations, Coronary Heart Disease, Illness Perception Intervention, Randomized Controlled Trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
124 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Medical Care
Arm Type
No Intervention
Arm Description
Patients receive standard treatment protocol for Coronary Artery Bypass Graft Surgery
Arm Title
Attention Control Group
Arm Type
Active Comparator
Arm Description
In addition to standard medical care patients receive a comparable amount of therapist´s attention (common and unspecific factors = supportive therapy) to the intervention group, without targeting patients' expectations.
Arm Title
Expectation Manipulation Intervention
Arm Type
Experimental
Arm Description
In addition to standard medical care patients' expectations prior to surgery are targeted in a brief psycho-educational intervention.
Intervention Type
Behavioral
Intervention Name(s)
Expectation Manipulation Intervention
Intervention Description
The Expectation Manipulation Intervention targets patients' expectations prior to surgery (2 individual sessions, 2 phone calls). Main goal is to enhance positive outcome expectancies, as well as to improve patients' control expectations about possible side effects of the surgery and about their personal management of their coronary heart disease. Further EMI tries to correct dysfunctional beliefs about the coronary heart disease and tries to minimize fears about expected negative consequences.
Intervention Type
Behavioral
Intervention Name(s)
Supportive Therapy
Intervention Description
Supportive therapy employs common factors such as elicitation of affect, reflective listening, feeling understood, but provides no explicit theoretical formulation to the patient. Supportive therapy thus provides a control condition for common factors and therapist attention but lacks the specific intervention part. It will be delivered in the same frequency and at the same time points as the Expectation Manipulation Intervention (2 individual sessions, 2 phone calls).
Primary Outcome Measure Information:
Title
Disability 6 months after surgery, controlled for baseline disability (Pain Disability Index; PDI)
Time Frame
6 months after surgery
Secondary Outcome Measure Information:
Title
Change in Patients' Expectations from Baseline/Pre-Intervention (expected average of 10 days before surgery) to hospital admission/Post-Intervention (expected average of 1 day before surgery).
Description
Prospective Illness Perception 6 months after surgery (Expected Illness Perception Questionnaire; IPQ-E), Positive Health Expectation Scale (PHES), Expected Disability (PDI-E)
Time Frame
From 10 days before surgery untill 1 day before surgery
Title
Change in Cardiac Anxiety (Cardiac Anxiety Questionnaire; CAQ) from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery
Title
Change in Physical Activity (International Physical Activity Questionnaire; IPAQ) from Baseline (an expected average of 10 days before surgery) to 6 months after surgery.
Time Frame
From 10 days before surgery to 6 months after surgery
Title
Change in Health Related Quality of Life (SF-12) from Baseline (expected average of 10 days before surgery) to 6 months after surgery.
Time Frame
From 10 days before surgery to 6 months after surgery
Title
Change in physical symptoms, subjective side effects and post-surgery complaints (Generic Assessment of Side Effects Scale; GASE-P)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery
Title
Change in Hospital Anxiety and Depression Scale (HADS)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Title
Change in Beliefs about Medications (Beliefs about Medications Questionaire; BMQ)from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Title
Change in Working ability from Baseline (expected average of 10 days before surgery) to 6 months after surgery.
Time Frame
From 10 days before surgery to 6 months after surgery.
Title
Satisfaction wiht the intervention.
Time Frame
Expected average of 1 day before surgery (but after the intervention).
Title
Cardiothoracic surgeons' rating of the surgery success
Time Frame
Expected average of 1 day after surgery
Title
Additional treatments during follow-up
Description
Additional Treatments, rehospitalizations, cardiac sport groups, rehabilitations programms, etc.
Time Frame
6 months after surgery
Title
Blinded Expert Rating of medical and psychological status at follow-up
Time Frame
6 months after surgery
Title
Change in Sleep Quality from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Title
Change in neuroendocrine and immunological measures from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Description
cortisol, inflammatory processes, catecholamines
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Title
Patient Pre-/Peri-/Postoperative Health Status retrospectively collected from patient file
Description
From Patient file: Left ventricular ejection fraction (EF), Body Mass Index, Blood pressure, Smoking status, Cardiac Operative Risk (EuroSCORE), New York Heart Association classification (NYHA), Canadian Cardiovascular Society grading of angina pectoris (CCS), Number of diseased coronary vessels, Previous myocardial infarctions, extra-cardiac arteriopathy, non-cardiac comorbidities, surgery procedure, surgery complications and in-hospital post surgery complications, time spent on the intensive care unit, inpatient days until discharge
Time Frame
6 months after surgery
Title
Patients' experience with prior surgeries
Description
Rating of experience with own prior surgeries. Rating of experience with surgeries of close others.
Time Frame
Baseline (expected average of 10 days before surgery)
Title
Enriched Social Support Inventory
Time Frame
Baseline (expected average 10 days before surgery)
Title
Occurrence of major life events since surgery
Time Frame
6 months after surgery
Title
Change in Patients' Illness Perception (Brief Illness Perception Questionnaire (B-IPQ) from 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery.
Time Frame
From 10 days before surgery to 1 day before surgery to 10 days after surgery to 6 months after surgery
Title
Satisfaction with the intervention
Time Frame
6 months after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled on the elective waiting list for first time coronary artery bypass graft surgery wiht the use of heart-lung-apparatus at the Department of Cardiovascular Surgery, Medical School, University of Marburg Sufficient knowledge of German language Ability to give informed consent Exclusion Criteria: Emergency surgery Presence of a serious comorbid psychiatric condition Presence of a life threatening comorbid medical condition Current participation in other research
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Winfried Rief, Prof. Dr.
Organizational Affiliation
Department of Clinical Psychology and Psychothearpy, Philipps University of Marburg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rainer Moosdorf, Prof. Dr.
Organizational Affiliation
Department of Cardiac and Thoracic Vessel Surgery, Heart Centre, Philipps University of Marburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Philipps University of Marburg
City
Marburg
State/Province
Hessen
ZIP/Postal Code
35032
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
23237127
Citation
Laferton JA, Shedden Mora M, Auer CJ, Moosdorf R, Rief W. Enhancing the efficacy of heart surgery by optimizing patients' preoperative expectations: study protocol of a randomized controlled trial. Am Heart J. 2013 Jan;165(1):1-7. doi: 10.1016/j.ahj.2012.10.007. Epub 2012 Nov 14.
Results Reference
background
PubMed Identifier
35522399
Citation
Horn N, Laferton JAC, Shedden-Mora MC, Moosdorf R, Rief W, Salzmann S. Baseline depressive symptoms, personal control, and concern moderate the effects of preoperative psychological interventions: the randomized controlled PSY-HEART trial. J Behav Med. 2022 Jun;45(3):350-365. doi: 10.1007/s10865-022-00319-0. Epub 2022 May 6.
Results Reference
derived
PubMed Identifier
33002633
Citation
Salzmann S, Euteneuer F, Laferton JAC, Shedden-Mora MC, Schedlowski M, Moosdorf R, Rief W. IL-8 and CRP moderate the effects of preoperative psychological interventions on postoperative long-term outcomes 6 months after CABG surgery - The randomized controlled PSY-HEART trial. Brain Behav Immun. 2021 Jan;91:202-211. doi: 10.1016/j.bbi.2020.09.028. Epub 2020 Sep 28.
Results Reference
derived
PubMed Identifier
28846584
Citation
Salzmann S, Euteneuer F, Laferton JAC, Auer CJ, Shedden-Mora MC, Schedlowski M, Moosdorf R, Rief W. Effects of Preoperative Psychological Interventions on Catecholamine and Cortisol Levels After Surgery in Coronary Artery Bypass Graft Patients: The Randomized Controlled PSY-HEART Trial. Psychosom Med. 2017 Sep;79(7):806-814. doi: 10.1097/PSY.0000000000000483.
Results Reference
derived
PubMed Identifier
28606503
Citation
Auer CJ, Laferton JAC, Shedden-Mora MC, Salzmann S, Moosdorf R, Rief W. Optimizing preoperative expectations leads to a shorter length of hospital stay in CABG patients: Further results of the randomized controlled PSY-HEART trial. J Psychosom Res. 2017 Jun;97:82-89. doi: 10.1016/j.jpsychores.2017.04.008. Epub 2017 Apr 19.
Results Reference
derived
PubMed Identifier
28069021
Citation
Rief W, Shedden-Mora MC, Laferton JA, Auer C, Petrie KJ, Salzmann S, Schedlowski M, Moosdorf R. Preoperative optimization of patient expectations improves long-term outcome in heart surgery patients: results of the randomized controlled PSY-HEART trial. BMC Med. 2017 Jan 10;15(1):4. doi: 10.1186/s12916-016-0767-3.
Results Reference
derived
Links:
URL
http://placeboforschung.de/
Description
Homepage of the transregional DFG research unit FOR 1328: Expectation and conditioning as basic processes of the placebo and nocebo response: From neurobiology to clinical applications

Learn more about this trial

Optimizing Expectations in Cardiac Surgery Patients

We'll reach out to this number within 24 hrs