Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04502121
Other study ID # ValvEx
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 17, 2020
Est. completion date July 7, 2023

Study information

Verified date September 2023
Source Philipps University Marburg Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recovery after surgery depends on psychological factors such as preoperative information, expectations and surgery-associated anxiety. Prior studies have shown that even short preoperative psychological interventions can improve postoperative outcomes in heart surgery patients. However, what content works best for which patient group and how long an intervention has to be is still largely unknown. The aims of this study are thus to examine if the developed preoperative psychological intervention (i) reduces preoperative anxiety, (ii) increases positive expectations, and (iii) improves the long-term outcome postoperative recovery. Therefore, a brief intervention has been developed. Heart valve patients who undergo a heart surgery will be randomized into two groups (Control vs. intervention group) after baseline assessment. Following this the intervention group will participate in the psychological intervention (30-40 minutes). To increase patients' positive expectations the intervention will focus on treatment outcome expectations and personal control expectations. Furthermore, patients in the intervention group will have two booster-telephone calls (four and eight weeks after the surgery) to check if their developed plans work out. The control group will receive the standard medical procedure. Both groups will fill out questionnaires again at the evening before the surgery, around one week after the surgery and three months after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date July 7, 2023
Est. primary completion date November 29, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who are scheduled for elective cardiac valve procedure - Age 18 or above - Fluency in German - Informed consent Exclusion Criteria: - Comorbid medical/psychiatric condition that causes more extensive disability than the coronary condition - Participation in other research programs: in agreement with Coordinating Investigator patient can participate substudies, if this do not interfere with the main study - Emergency surgery

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
EXPECT: Preoperative optimization of cardiac valve patient's expectations
The psychological, preoperative intervention follows a treatment manual. Patients get a personal intervention one day before surgery (30-40 minutes). It includes the development of an individual, subjectively perceived disease model, the treatment outcome expectations and the personalized outcome expectancy. Additionally they get two booster telephone calls 4 and 8 weeks after the surgery to recall the discussed topics and to talk about their recovery process (10-15 minutes).

Locations

Country Name City State
Germany UKGM Marburg Marburg

Sponsors (3)

Lead Sponsor Collaborator
Philipps University Marburg Medical Center Heart Centre Rotenburg, Justus-Liebig University Gießen Medical Center

Country where clinical trial is conducted

Germany, 

References & Publications (15)

Auer CJ, Glombiewski JA, Doering BK, Winkler A, Laferton JA, Broadbent E, Rief W. Patients' Expectations Predict Surgery Outcomes: A Meta-Analysis. Int J Behav Med. 2016 Feb;23(1):49-62. doi: 10.1007/s12529-015-9500-4. — View Citation

Broadbent E, Petrie KJ, Main J, Weinman J. The brief illness perception questionnaire. J Psychosom Res. 2006 Jun;60(6):631-7. doi: 10.1016/j.jpsychores.2005.10.020. — View Citation

Gaab, J. (2009). PASA-Primary Appraisal Secondary Appraisal-Ein Fragebogen zur Erfassung von situations-bezogenen kognitiven Bewertungen. Verhaltenstherapie, 19(2), 114-115.

Juergens MC, Seekatz B, Moosdorf RG, Petrie KJ, Rief W. Illness beliefs before cardiac surgery predict disability, quality of life, and depression 3 months later. J Psychosom Res. 2010 Jun;68(6):553-60. doi: 10.1016/j.jpsychores.2009.10.004. Epub 2009 Dec 5. — View Citation

Laferton JA, Kube T, Salzmann S, Auer CJ, Shedden-Mora MC. Patients' Expectations Regarding Medical Treatment: A Critical Review of Concepts and Their Assessment. Front Psychol. 2017 Feb 21;8:233. doi: 10.3389/fpsyg.2017.00233. eCollection 2017. — View Citation

Löwe, B., Spitzer, R. L., Zipfel, S., & Herzog, W. (2002). PHQ-D Gesundheitsfragebogen für Patienten (German Version of the Patient Health Questionnaire). Karlsruhe: Pfizer.

Moerman N, van Dam FS, Muller MJ, Oosting H. The Amsterdam Preoperative Anxiety and Information Scale (APAIS). Anesth Analg. 1996 Mar;82(3):445-51. doi: 10.1097/00000539-199603000-00002. — View Citation

Rammstedt, B. und O. P. John, 2007: Measuring personality in one minute or less: A 10-item short version of the Big Five Inventory in English and German. Journal of Research in Personality 41: 203-212

Rector TS, Kubo SH, Cohn JN. Validity of the Minnesota Living with Heart Failure questionnaire as a measure of therapeutic response to enalapril or placebo. Am J Cardiol. 1993 May 1;71(12):1106-7. doi: 10.1016/0002-9149(93)90582-w. No abstract available. — View 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. — View Citation

Rief, W., & Glombiewski, J. A. (2016). Erwartungsfokussierte Psychotherapeutische Interventionen (EFPI). Verhaltenstherapie, 26(1), 47-54.

Salzmann, S., Laferton, J., Auer, C., Shedden-Mora, M., Wambach, K., & Rief, W. (2018). Patientenerwartungen optimieren: Beschreibung einer präoperativen Kurzintervention am Beispiel von Patienten vor einer Bypass-Operation. Verhaltenstherapie, 28(3), 157-165.

Scheier MF, Carver CS, Bridges MW. Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): a reevaluation of the Life Orientation Test. J Pers Soc Psychol. 1994 Dec;67(6):1063-78. doi: 10.1037//0022-3514.67.6.1063. — View Citation

Spitzer RL, Kroenke K, Williams JB, Lowe B. A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med. 2006 May 22;166(10):1092-7. doi: 10.1001/archinte.166.10.1092. — View Citation

Ware J Jr, Kosinski M, Keller SD. A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996 Mar;34(3):220-33. doi: 10.1097/00005650-199603000-00003. — View Citation

* Note: There are 15 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Other Change in The Primary Appraisal Secondary Appraisal questionnaire (PASA) from Baseline to one day pre-surgery to one week post-surgery Items range from 0 (absolutely wrong) - 6 (absolutely right). Higher scores mean a better outcome. Baseline, one day pre-surgery, up to one week post-surgery
Other Change in Patients' Illness Perception (Brief Illness Perception Questionnaire, B-IPQ) from Baseline to 1 week post-surgery to 3 months after surgery The B-IPQ surveys the cognitive and emotional representations of illness. Item 1-5 measure cognitive illness representations (consequences, timeline, personal control, treatment control, andidentity). Item 6 and 8 quantify emotional representations (concern & emotions). Item 7 assesses illness comprehensibility. Item 9 is an open question (three most important causal factors in their illness). Items range from 0-10: item 1: no disability at all to very strong disability, item 2: really short to forever, item 3: no control at all zo extreme control, item 4: not at all to extremely helpful, item 5: no complaints at all to very much and strong complaints, item 6: no worries at all to extreme worries, item 7: not at all to very clear, item 8: emotionally not included at all to emotional extremely included. Baseline, up to one week post-surgery, up to three months post-surgery
Other Change in patients' expectations (Expected Illness Perception Questionnaire, IPQ-E) from Baseline to one week post-surgery to three months post-surgery Items range from 1 (absolutely wrong) - 5 (absolutely right). Higher scores mean a better outcome. Baseline, up to one week post-surgery, up to three months post-surgery
Other Change in patients optimism (Life-Orientation-Test Revised, LOT-R) from Baseline to one week post-surgery to three months post-surgery Items range from 1 (absolutely) - 5 (absolutely not). Higher scores mean a worse outcome. Baseline, up to one week post-surgery, up to three months post-surgery
Other Personality (Big Five Inventory, BFI-10) Items range from 1 (disagree strongly) - 5 (agree strongly). The questionnaire includes the scales "openness to experience", "conscientiousness", "extraversion", agreeableness and neuroticism. Baseline
Other Patients' experience with prior surgeries Rating of experience with own prior surgeries. Rating of experience with surgeries of close others. First patients are asked if they or close others had a prior surgery before (yes/no). If they answer yes, they are asked to rate their or their close others experience (item ranges from 1 (very bad) - 5 (very good). Baseline
Other Surgery procedure (planned and realized) The planned and the realized surgical approach (minimally invasive or open) will be noted. Baseline, up to one week post-surgery
Primary Change in Pain Disability Index (PDI) from Baseline to one day pre-surgery to one week post-surgery to three months post-surgery Items range from 0 (no disability at all) - 10 (total disability). Consequently higher scores mean a worse outcome. Baseline, one day pre-surgery, up to one week post-surgery, up to three months post-surgery
Secondary Change in Minnesota Living with Heart Failure Questionnaire (MLHFQ) from Baseline to one week post-surgery to three months post-surgery Items range from 0 (no restriction), 1 (nearly not restricted) - 5 (very strongly restricted). Consequently higher scores mean a worse outcome. Baseline, up to one week post-surgery, up to three months post-surgery
Secondary Change in Health Related Quality of Life (Short Form 12, SF-12) from Baseline to one week post-surgery to three months post-surgery There are different item scales. The item scale of the first item (General health perceptions) ranges from 1 (excellent) to 5 (bad). The item scales of the second and third item (limitations in physical activities because of health problems) range from 1 (yes, absolutely restricted) to 2 (yes, a bit restricted) to 3 (no, not restricted at all). The item scales of the items 4-7 (limitations in usual role activities because of physical health or emotional problems) are just "yes" and "no". The item scale of the eighth item (bodily pain) ranges from 1 (Absolutely not) to 5 (a lot). The item scales of the items 9-12 (general mental health, vitality and limitations in social activities because of physical or emotional problems) range from 1 (always) to 5 (never). Baseline, up to one week post-surgery, up to three months post-surgery
Secondary Change in Patient health questionnaire screener (PHQ) from Baseline to one week post-surgery to three months post-surgery Items range from 1 (not at all) - 4 (nearly everyday). Consequently higher scores mean a worse outcome. Baseline, up to one week post-surgery, up to three months post-surgery
Secondary Change in Generalized Anxiety Disorder 7 (GAD-7) from Baseline to one week post-surgery to three months post-surgery Items range from 1 (not at all) - 4 (nearly everyday). Consequently higher scores mean a worse outcome. Baseline, up to one week post-surgery, up to three months post-surgery
Secondary Change in Anxiety (The Amsterdam Preoperative Anxiety and Information Scale, APAIS) from Baseline to one day pre-surgery Items range from 1 (not at all) - 5 (extremely). Higher scores mean patients are more interested in information and do have greater worries. Baseline, one day pre-surgery
Secondary Days the patient stays in the hospital, days at the intensive care unit up to one week post-surgery
Secondary Change of Concentration of Inflammatory marker C-reactive protein (CRP) in mg/l Change from baseline to postoperative day 1 (POD1) to approx. POD2 to approx. POD 5; higher scores mean a worse outcome. Baseline, up to one day, two days and five days post-surgery
See also
  Status Clinical Trial Phase
Recruiting NCT05308719 - Nasal Oxygen Therapy After Cardiac Surgery N/A
Recruiting NCT06001489 - The Effects of 360-degree Virtual Reality on Pre-procedural Anxiety in Patients Awaiting Elective Cardiac Surgery Involving a Sternotomy N/A
Completed NCT02657109 - Influence of a Rehabilitation in Valve Replacement on Heart Rate Variability and Oxidative Stress N/A
Recruiting NCT06154473 - Assessment of Patients Undergoing Cardiac Surgery and Admitted to the Intensive Care Unit
Completed NCT03015025 - Pharmacogenetic Dosage Algorithm for Acenocoumarol N/A
Not yet recruiting NCT06076759 - Intrathecal Dexmedetomidine Versus Intrathecal Morphine Inpatients Undergoing Cardiac Valve Replacement Surgeries N/A
Recruiting NCT03825250 - The Val-CARD Trial Phase 1/Phase 2
Recruiting NCT05335902 - Optic Nerve Sheath After Extracorporeal Circulation
Withdrawn NCT03446599 - Hemodynamic Effects of Methylene Blue vs Hydroxocobalamin in Patients at Risk of Vasoplegia During Cardiac Surgery Phase 2
Recruiting NCT04015973 - The PRE-OP ENERGY Trial N/A
Not yet recruiting NCT03440268 - Prevention of Acute Kidney Injury by N-Acetylcystein in Patients Undergone Cardiac Valve Replacement Phase 4
Not yet recruiting NCT06144125 - Prothrombin Complex Concentrate vs Fresh Frozen Plasma in Goal-directed Bleeding Management in Cardiac Surgery Phase 4
Recruiting NCT05002543 - CORCYM Mitral, Aortic aNd Tricuspid Post-maRket Study in a reAl-world Setting
Active, not recruiting NCT03810820 - Remote ECG Monitoring of TAVI Patients N/A
Recruiting NCT05206929 - Cardiac Surgery Sternal Precautions N/A
Terminated NCT01236313 - Aortic Wall and Left Ventricular Mechanics: Echocardiographic and Hemodynamic Analysis N/A
Recruiting NCT04031144 - Ultrafiltration on Coagulation Function in Cardiac Surgery N/A
Withdrawn NCT04481490 - A Study to Objectively Measure Physical Activity and Sedentary Behavior During Cardiac Rehabilitation
Active, not recruiting NCT01783483 - An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery Phase 4
Recruiting NCT05506293 - European Multicentre Registry of Percutaneous Paravalvular Leak Closure