RECRUITING

Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Myotonic dystrophy (DM) and facioscapulohumeral muscular dystrophy (FSHD) are inherited disorders characterized by progressive muscle weakness and loss of muscle tissue. The purpose of this registry is to connect people with DM or FSHD with researchers studying these diseases. The registry will offer individuals with DM and FSHD an opportunity to participate in research that focuses of their diseases. The registry will also help scientists to accomplish research on DM and FSHD and to distribute their findings to patients and care providers.

Official Title

National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Patients and Family Members

Quick Facts

Study Start:2000-09
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT00082108

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Diagnosed with DM, FSHD, or related diseases or are an unaffected family member of someone diagnosed with one of these diseases
  1. * No family history of DM, FSHD, or related diseases

Contacts and Locations

Study Contact

Registry Coordinator
CONTACT
888-925-4302
dystrophy_registry@urmc.rochester.edu

Principal Investigator

Richard T. Moxley, III, MD
PRINCIPAL_INVESTIGATOR
University of Rochester Medical Center, Department of Neurology

Study Locations (Sites)

University of Rochester Medical Center, Department of Neurology
Rochester, New York, 14642
United States

Collaborators and Investigators

Sponsor: University of Rochester

  • Richard T. Moxley, III, MD, PRINCIPAL_INVESTIGATOR, University of Rochester Medical Center, Department of Neurology

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2000-09
Study Completion Date2025-06

Study Record Updates

Study Start Date2000-09
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • Registry
  • FSHD
  • DM
  • Muscular Dystrophy
  • Facioscapulohumeral Myotonic Dystrophy
  • Myotonic Dystrophy
  • DM1
  • DM2
  • FSH
  • MMD

Additional Relevant MeSH Terms

  • Myotonic Dystrophy
  • Facioscapulohumeral Muscular Dystrophy
  • Muscular Dystrophy
  • Myotonic Dystrophy Type 1
  • Myotonic Dystrophy Type 2
  • Congenital Myotonic Dystrophy
  • PROMM (Proximal Myotonic Myopathy)
  • Steinert's Disease
  • Myotonic Muscular Dystrophy