Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry
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Purpose
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.
| Condition |
|---|
|
Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Patients and Family Members |
- Patient reported outcomes [ Time Frame: Annual ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 2300 |
| Study Start Date: | September 2000 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | June 2013 (Final data collection date for primary outcome measure) |
The National Registry of DM and FSHD Patients and Family Members was developed to create a link between patients and scientists in order to promote research on these rare illnesses. The Registry is sponsored by the National Institutes of Health.
Patients that are interested in joining the Registry can email or call to request an application or download the forms from the website (www.dystrophyregistry.org). The Application packet contains:
- A Patient Information Form, which asks about your muscle strength, general health, and how your disease affects your daily life
- A Medical Records Release Form, which allows us to contact your doctor and obtain records about your diagnosis
- An informed Consent Form, which describes the study's purpose and what you can expect while you are involved with the project.
After you are enrolled in the Registry, there are several ways to participate in research. The activities include:
- Complete an annual update form to help us keep track of how your symptoms change over time.
- Receive a newsletter once a year about the progress of the Registry, research highlights, and other news related to muscular dystrophy.
- Receive a letter from the Registry when researchers are looking for patients to take part in studies. These projects may include filling out questionnaires, exploring new treatments and other types of research.
There is no obligation to participate in these activities. Taking part in any study or filling out the annual updates are completely up to you.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Participants will volunteer to participate in this study. The study will be advertised through neuromuscular disease clinics, the National Registry website, Patient Advocacy Groups and MDA Clinics through out the United States.
Inclusion Criteria:
- Diagnosed with DM, FSHD, or related diseases or are an unaffected family member of someone diagnosed with one of these diseases
Exclusion Criteria:
- No family history of DM, FSHD, or related diseases
Contacts and Locations| Contact: Registry Coordinator | 888-925-4302 | dystrophy_registry@urmc.rochester.edu |
| United States, New York | |
| University of Rochester Medical Center, Department of Neurology | Recruiting |
| Rochester, New York, United States, 14642 | |
| Contact: Registry Coordinator 888-925-4302 dystrophy_registry@urmc.rochester.edu | |
| Principal Investigator: Richard T. Moxley, III, MD | |
| Sub-Investigator: Rabi Tawil, MD | |
| Principal Investigator: | Richard T. Moxley, III, MD | University of Rochester Medical Center, Department of Neurology |
More Information
Additional Information:
No publications provided
| Responsible Party: | Richard T Moxley, Professor of Neurology, University of Rochester |
| ClinicalTrials.gov Identifier: | NCT00082108 History of Changes |
| Other Study ID Numbers: | NIAMS-104, U54NS048843 |
| Study First Received: | April 29, 2004 |
| Last Updated: | January 31, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of Rochester:
|
Registry FSHD DM |
Muscular Dystrophy Facioscapulohumeral Myotonic Dystrophy Myotonic Dystrophy |
Additional relevant MeSH terms:
|
Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophies Myotonic Dystrophy Muscular Disorders, Atrophic Muscular Diseases Musculoskeletal Diseases |
Neuromuscular Diseases Nervous System Diseases Genetic Diseases, Inborn Myotonic Disorders Heredodegenerative Disorders, Nervous System Neurodegenerative Diseases |
ClinicalTrials.gov processed this record on May 23, 2013