Back to search results

A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study

Abroad (travel likely)Recruiting

Conditions

Patient-Reported Outcome Measures (PROMs) · Pragmatic Trial · Adolescent Congenital Heart Disease · Resiliency-building Intervention · Resilience, Psychological · Telemedicine-Based Education

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • Stanford School of Medicine, Stanford, California, United States

    Contact: Study coordinator (Lauren M Schneider, PsyD) · lmikula@stanford.edu · 650-723-5511

  • Children's Hospital Colorado, Aurora, Colorado, United States

    Contact: Study coordinator (Sarah L Kelly, PsyD) · sarah.kelly@childrenscolorado.org · 720-777-4599
    Contact: Principal Investigator (Sarah Kelly, PsyD)

  • Emory University School of Medicine, Atlanta, Georgia, United States

    Contact: Study coordinator (Kolby Sanders-Lewis) · Kolby.sanders-lewis@choa.org
    Contact: Principal Investigator (Lazaros Kochilas, MD, MSCR)

  • University of Kentucky College of Medicine, Lexington, Kentucky, United States

    Contact: Study coordinator (Heather Collins) · heather.collins1@uky.edu · 859-562-1103
    Contact: Principal Investigator (Louis I Bezold, MD)

  • Boston Children's Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Zoe Wernsing) · Zoe.wernsing@childrens.harvard.edu · 617-355-4266
    Contact: Study coordinator (Thomas Giorgio) · Thomas.giorgio@cardio.chboston.org · 617-355-4201
    Contact: Principal Investigator (Sarah de Ferranti, MD, MPH)

  • University of Michigan Health System, Ann Arbor, Michigan, United States

    Contact: Study coordinator (Adriana Batazzi) · batazzia@med.umich.edu · 732-615-2369
    Contact: Principal Investigator (Kurt Schumacher, MD, MS)

  • Washington University School of Medicine, St Louis, Missouri, United States

    Contact: Study coordinator (Aecha M Ybarra, MD, MS) · amybarra@wustl.edu

  • Icahn School of Medicine at Mount Sinai, New York, New York, United States

    Contact: Study coordinator (Xuery Mu) · xueru.mu@mssm.edu · 347-335-7148
    Contact: Principal Investigator (Brett Anderson, MD, MBA, MS)

  • Columbia University Irving Medical Center, New York, New York, United States

    Contact: Study coordinator (Michael P DiLorenzo, MD, MSCE) · mpd2001@cumc.columbia.edu · 212-342-1562
    Contact: Principal Investigator (Michael DiLorenzo, MD, MSCE)

  • Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States

    Contact: Study coordinator (Paul J Critser, MD, PhD) · Paul.Critser@cchmc.org · 513-517-1523

  • Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Andrea L Jones, MD, MSCE) · jonesa21@chop.edu

  • Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States

    Contact: Study coordinator (Bryan Goldstein, MD) · bryan.goldstein@chp.edu
    Contact: Principal Investigator (Bryan Goldstein, MD)

  • Medical University of South Carolina, Charleston, South Carolina, United States

    Contact: Study coordinator (Eric Graham, MD) · grahamem@musc.edu
    Contact: Principal Investigator (Eric Graham, MD)

  • Primary Children's Hospital, University of Utah, Salt Lake City, Utah, United States

    Contact: Study coordinator (Laura Wood, PhD) · laura.k.wood@hsc.utah.edu · 713-557-4868
Study leads

  • Melissa Cousino, PhD

    Principal Investigator

    University of Michigan

View source on ClinicalTrials.gov(opens in a new tab)