The DCM Project Portal: A direct-to-participant platform of The DCM Research Project.

Research design dilated cardiomyopathy family members

Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
29 Jun 2023
Historique:
pubmed: 10 7 2023
medline: 10 7 2023
entrez: 10 7 2023
Statut: epublish

Résumé

To develop a digital platform to conduct family-based, dilated cardiomyopathy (DCM) genetic research. Innovative approaches are needed to achieve large family enrollment targets. The DCM Project Portal, a direct-to-participant electronic recruitment, consent, and communication tool, was designed using prior experience with traditional enrollment methods, characteristics and feedback of current participants, and internet access of the US population. DCM patients (probands) and their family members. The portal was designed as a self-guided, three module (registration, eligibility, and consent) process with internally created supporting informational and messaging resources integrated throughout. The experience can be tailored to user type and the format adapted with programmatic growth. Characteristics of participants of the recently completed DCM Precision Medicine Study were assessed as an exemplary user population. A majority of the diverse (34% non-Hispanic Black (NHE-B), 9.1% Hispanic; 53.6% female) proband (n=1223) and family members (n=1781) participants aged ≥18 years reported Digital enrollment tools offer opportunity to improve access and efficiency. The portal is an example of a digital approach to family-based genetic research.

Identifiants

pubmed: 37425710
doi: 10.1101/2023.06.22.23291764
pmc: PMC10327249
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL128857
Pays : United States

Déclaration de conflit d'intérêts

Disclosures The authors have no relevant disclosures.

Auteurs

Elizabeth S Jordan (ES)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Phoenix L Grover (PL)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Jay Lin (J)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Carl A Starkey (CA)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Elizabeth A Finley (EA)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Hanyu Ni (H)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Ray E Hershberger (RE)

The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.
Division of Cardiovascular Medicine, Department of Internal Medicine, The Ohio State University, Columbus, OH.

Classifications MeSH