THORESCI: Tilburg Health Outcomes Registry of Emotional Stress in Coronary Intervention

Sponsor
Tilburg University (Other)
Overall Status
Recruiting
CT.gov ID
NCT02621216
Collaborator
The Elisabeth-TweeSteden Hospital (Other), Elisabeth-TweeSteden Ziekenhuis (Other)
3,000
1
120
25

Study Details

Study Description

Brief Summary

Background of the study:

Percutaneous coronary interventions (PCI) have become mainstay treatment for acute coronary artery disease and the number of patients receiving PCI is vastly growing. However, relatively little long-term follow-up studies of large real-world clinical samples exist that have looked at the real-world effects of PCI treatment and adherence to current guidelines.

Psychological risk factors are important in determining prognosis after PCI, and undergoing PCI may increase the risk of low mood. To date, studies have examined single psychological risk factors, without taking into account their relatedness. Moreover, guidelines are advocating psychosocial screening in early cardiovascular disease, but the screening test as proposed in the prevention guideline has not yet been validated or tested. Although the detrimental effects of psychological risk factors on cardiovascular prognosis are known, the mechanisms through which they exert these effects are yet unclear. It is to be expected that not one but multiple biological (inflammation, endothelial dysfunction) and behavioural (coping styles, poor self-care, consultation behaviour) pathophysiological processes play a role, and that these processes interact with each other. In PCI patients the mechanisms linking psychological risk to poor prognosis are still to be investigated.

Objective of the study:
  1. To examine the adherence to the prevention and PCI guidelines and the effects thereof on long term prognosis in PCI patients.

  2. To evaluate the effectiveness of the psychosocial screening instrument of the European Society of Cardiology Prevention guideline 2012.

  3. To examine effects of clustering psychological risk factors on several networks of potentially mediating mechanisms and long term outcomes in a large sample of PCI patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Rationale: Percutaneous coronary interventions (PCI) have become mainstay treatment for acute coronary artery disease and the number of patients receiving PCI is vastly growing. Clinical trials have reported on the efficacy and effects on quality of life and mortality. Guidelines have been constructed for PCI treatment as well as cardiovascular prevention. However, relatively little long-term follow-up studies of large real-world clinical samples exist that have looked at the real-world effects of PCI treatment and adherence to current guidelines.

    Moreover, psychological risk factors are important in determining prognosis after PCI, and undergoing PCI may increase the risk of low mood. To date, studies have examined single psychological risk factors, without taking into account their relatedness. Moreover, guidelines are advocating psychosocial screening in early cardiovascular disease, but the screening test as proposed in the ESC Prevention guideline has not yet been validated or tested.

    Although the detrimental effects of psychological risk factors on cardiovascular prognosis are known, the mechanisms through which they exert these effects are yet unclear. It is to be expected that not one but multiple biological (inflammation, endothelial dysfunction) and behavioural (coping styles, poor self-care, consultation behaviour) pathological processes play a role, and that these processes interact with each other. In PCI patients, the mechanisms linking psychological risk to poor prognosis are still to be investigated. Objective: (1) To examine the adherence to the prevention and PCI guidelines and the effects thereof on long term prognosis in PCI patients. (2) To examine effects of clustering psychological risk factors on several networks of potentially mediating mechanisms and long term outcomes in a large sample of PCI patients. (3) To evaluate the effectiveness of the psychosocial screening instrument of the European Society of Cardiology Prevention guideline 2012. Study design: Prospective observational cohort study. Study population: All patients aged >18 admitted to the TweeSteden hospital for percutaneous coronary intervention are eligible. Main study parameters/endpoints: Predictors: Psychological (risk) factors (depression, anxiety, Type D personality, mindfulness, positive mood), Adherence; Outcome variables: PCI complications, hospitalizations, events. Potential mediators: inflammatory biomarkers, markers of endothelial dysfunction, physical stress recovery) Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The risk associated with the current study is very low. For this mechanistic observational study, investigators will ask patients to fill out two extensive (20 pages) and then several smaller (12-15 pages) psychological surveys including among others questions on personality, positive and negative mood, mindfulness, work stress, and satisfaction with life. Preferably, questionnaires will be administered digitally by email link. In addition, in a subsample three additional fasting blood samples will be drawn to assess study-specific markers, of which two will coincide with regular blood draws at the clinic. There are no direct benefits of participation, other than providing data to create knowledge to improve future treatment.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    3000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Tilburg Health Outcomes Registry of Emotional Stress in Coronary Intervention
    Study Start Date :
    Dec 1, 2013
    Anticipated Primary Completion Date :
    Dec 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. PCI complications [1 year]

      procedure related complications, events and mortality in the first year post-PCI

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • PCI

    • Sufficient understanding of Dutch language

    Exclusion Criteria:
    • life threatening comorbidity (e.g., metastasized cancer)

    • cognitive disorder

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Elisabeth-TweeSteden hospital Tilburg Noord-Brabant Netherlands 5042AD

    Sponsors and Collaborators

    • Tilburg University
    • The Elisabeth-TweeSteden Hospital
    • Elisabeth-TweeSteden Ziekenhuis

    Investigators

    • Principal Investigator: Nina Kupper, PhD, Tilburg University

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Nina Kupper PhD, Associate Professor of Medical Psychology, Tilburg University
    ClinicalTrials.gov Identifier:
    NCT02621216
    Other Study ID Numbers:
    • THORESCI
    • NL46259.028.13
    First Posted:
    Dec 3, 2015
    Last Update Posted:
    Oct 30, 2017
    Last Verified:
    Oct 1, 2017
    Keywords provided by Nina Kupper PhD, Associate Professor of Medical Psychology, Tilburg University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 30, 2017