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DCM Precision Medicine Study

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ClinicalTrials.gov Identifier: NCT03037632
Recruitment Status : Recruiting
First Posted : January 31, 2017
Last Update Posted : March 27, 2018
Sponsor:
Collaborators:
National Heart, Lung, and Blood Institute (NHLBI)
National Human Genome Research Institute (NHGRI)
Information provided by (Responsible Party):
Ray Hershberger, Ohio State University

January 27, 2017
January 31, 2017
March 27, 2018
June 7, 2016
June 2019   (Final data collection date for primary outcome measure)
  • Family clinical screening completed within 12 months from proband enrollment. [ Time Frame: 12 months from proband enrollment. ]
    The probability that a living first-degree relative (FDR) without a previous definitive DCM diagnosis completes clinical screening for DCM within 12 months after proband recruitment
  • Living first-degree relative adheres to cardiovascular surveillance recommendations after return of genetic results. [ Time Frame: 2.5 years ]
    The probability that a living first-degree relative adheres to surveillance recommendations within 15 months after the proband receives individual genetic test information.
Same as current
Complete list of historical versions of study NCT03037632 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
DCM Precision Medicine Study
Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry
The aims of the DCM Precision Medicine Study are to test the hypothesis that DCM has substantial genetic basis and to evaluate the effectiveness of a family communication intervention in improving the uptake and impact of family member clinical screening.
Dilated cardiomyopathy of unknown cause (DCM), known clinically as idiopathic dilated cardiomypathy, is the most common cardiomyopathy and is the leading cause of heart transplantation. DCM affects approximately one million individuals, and so has a major impact on US public health. DCM is commonly asymptomatic until very late in its course when it causes heart failure, disability, and death. Because of its clinical course, any means to identify patients at risk for DCM or to detect DCM in its asymptomatic phase could provide enormous opportunity for intervention to extend lives and prevent late-stage disease. Within this paradigm precision medicine for DCM could greatly impact health care outcomes and costs. Recent advances in DCM genetics have introduced these possibilities, but unresolved questions of familial recurrence risk, genetic etiology, racial differences, and family-based screening must be addressed to move ahead. The central hypothesis of this study, based on published studies of the investigative group, states that DCM has substantial genetic basis. For this study the investigators hypothesize that: (a) 35% of probands of both European and African ancestry (EA/AA) will be classified as familial in a cohort recruited in a multicenter US consortium and given explicit recommendations and assistance to achieve the clinical screening of relatives; (b) approximately 40% of DCM probands, whether categorized as familial or non-familial, or as EA or AA, will have pathogenic or likely pathogenic variants in genes previously implicated in DCM; and (c) a tailored intervention to help DCM probands communicate DCM risk to their family members will improve the uptake and impact of necessary clinical and genetic testing. To test these hypotheses, the investigators propose to: (1) estimate and compare the frequencies of EA and AA DCM probands classified as having familial DCM; (2) estimate and compare the proportions of probands with an identifiable genetic cause of DCM in groups defined by proband classification (familial/non-familial) and ancestry (EA/AA); and (3) evaluate the impact of a randomized intervention to aid and direct family communication on participation of at-risk family members in clinical screening and appropriate follow-up surveillance for DCM. These aims will be accomplished by recruiting a cohort of 1300 DCM probands (600 EA, 600 AA, 100 Hispanic ethnicity), performing cardiovascular clinical screening of 2600 family members, performing genetic testing of probands and affected family members by exome sequencing, returning genetic results, and randomizing probands to an intervention to improve family communication regarding DCM risk. Proving these hypotheses would be transformative for the field: rather than viewing DCM as only a clinical diagnosis, cardiovascular professionals would understand DCM as a genetic disease that should be managed using genetic diagnostic and family-based preventive strategies. These study results would make precision medicine for DCM a reality.
Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Masking Description:
Blinded until intervention is assigned to subject.
Primary Purpose: Prevention
Idiopathic Dilated Cardiomyopathy
Behavioral: Family Heart Talk Booklet
  • Experimental: Communication Tool
    Intervention: Behavioral: Family Heart Talk Booklet
  • No Intervention: No Communication Tool
Kinnamon DD, Morales A, Bowen DJ, Burke W, Hershberger RE; DCM Consortium*. Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study. Circ Cardiovasc Genet. 2017 Dec;10(6). pii: e001826. doi: 10.1161/CIRCGENETICS.117.001826.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
6500
Same as current
June 2021
June 2019   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Meeting criteria for dilated cardiomyopathy (DCM) :

    • Left ventricular ejection fraction <50%
    • Left ventricular enlargement (A left ventricular end-diastolic dimension > 95%tile population standard based on gender and height).
  • Detectable causes of cardiomyopathy, except genetic, excluded beyond a reasonable doubt at the time of DCM diagnosis (that is, meeting clinical criteria for idiopathic DCM)
  • Any age (including children)
  • Non-Hispanic and Hispanic ethnicity
  • All races (PI pre-approval required for recruitment beyond pre-specified recruitment targets).
  • Ability to give informed consent
  • Ability to communicate in English (except Spanish language at sites approved to recruit individuals of Hispanic ethnicity)
  • Willingness to participate in a family-based study (patient willing to work with a clinical site and/or OSU to facilitate the recruitment and enrollment of family members to the study).

Exclusion Criteria:

  • Coronary artery disease (CAD) causing ischemic cardiomyopathy (> 50% narrowing, any major epicardial coronary artery)
  • Primary valvular disease
  • Adriamycin or other cardiotoxic drug exposure
  • Other forms of cardiomyopathy: Hypertrophic, Restrictive, or Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
  • Congenital heart disease
  • Other detectable causes of dilated cardiomyopathy, including sarcoid and hemochromatosis.
  • Other active multi-system disease that may cause DCM (e.g., active connective tissue disease).
  • Severe and untreated or untreatable hypertension (systolic blood pressures routinely greater than 180 mm Hg and/or diastolic blood pressures greater than 120 mm Hg, and if resistant to multidrug treatment).
  • However, conventional risk factors for DCM, including obesity, routinely treated hypertension, alcohol use, pregnancy or the peri-partum period, or left ventricular noncompaction, will NOT be considered exclusion criteria.
Sexes Eligible for Study: All
Child, Adult, Older Adult
No
Contact: Principal Investigator 614-688-1388
Contact: Clinical Research Manager 614-688-9815
United States
 
 
NCT03037632
2015H0309
R01HL128857 ( U.S. NIH Grant/Contract )
Yes
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: No
Ray Hershberger, Ohio State University
Ray Hershberger
  • National Heart, Lung, and Blood Institute (NHLBI)
  • National Human Genome Research Institute (NHGRI)
Principal Investigator: Ray Hershberger, MD Ohio State University
Ohio State University
March 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP