Trial record 3 of 13 for:    "Stress cardiomyopathy"

Personality Profile of Patients With Apical Ballooning Syndrome

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
Abhiram Prasad, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01885975
First received: June 20, 2013
Last updated: January 17, 2014
Last verified: January 2014
  Purpose

The investigators' hypothesis is that patients with apical ballooning syndrome (ABS) will manifest a personality profile that differs than that of a population of similar range of ethnic and socioeconomic status.


Condition
Apical Ballooning Syndrome

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Personality Profile of Patients With Apical Ballooning Syndrome (ABS)

Resource links provided by NLM:


Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • Range of personality traits as assessed by the "NEO-PI-3" [ Time Frame: Baseline: the traits will be assessed once upon enrollment into the study ] [ Designated as safety issue: No ]

    The "NEO PI-3" measures the five major domains of personality, which are:

    • Neuroticism
    • Extraversion
    • Openness
    • Agreeableness
    • Conscientiousness


Estimated Enrollment: 213
Study Start Date: July 2013
Estimated Study Completion Date: July 2014
Estimated Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

This study will be conducted among participants in the Mayo Clinic Apical Ballooning Registry. These patients were prospectively diagnosed with Apical Ballooning Syndrome at the time of presentation with their acute illness, and consented to participation in a registry. They are residents of Olmsted County, and the surrounding regions for which the Mayo Clinic serves as a tertiary care center. Enrollment in the registry requires satisfaction of standard criteria for the diagnosis of ABS and includes the administration of a standardized questionnaire. Subjects have agreed to participate in yearly follow up questionnaires about their health status.

Criteria

Inclusion criteria:

  1. Patients who have suffered with ABS
  2. Adults (18 years or older)
  3. Able to read English at a 6th grade level (questionnaires are self-administered and written in English)

Exclusion criteria:

  1. Have withdrawn from the registry
  2. Have died
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01885975

Locations
United States, Minnesota
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Investigators
Principal Investigator: Abhiram Prasad, MD Mayo Clinic
  More Information

No publications provided

Responsible Party: Abhiram Prasad, PI, Mayo Clinic
ClinicalTrials.gov Identifier: NCT01885975     History of Changes
Other Study ID Numbers: 13-003419
Study First Received: June 20, 2013
Last Updated: January 17, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by Mayo Clinic:
Apical Ballooning syndrome
Personality

Additional relevant MeSH terms:
Takotsubo Cardiomyopathy
Ventricular Dysfunction, Left
Ventricular Dysfunction
Heart Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on July 31, 2014