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| ID | Type | Description | Link |
|---|---|---|---|
| 5U54NS064808-07 | U.S. NIH Grant/Contract | View source | |
| INC6606 | Other Identifier | Inherited Neuropathies Consortium |
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| Name | Class |
|---|---|
| University of Rochester | OTHER |
| National Institute of Neurological Disorders and Stroke (NINDS) | NIH |
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The purpose of this study is to identify the issues that have greatest impact on QOL for patients with Charcot Marie Tooth (CMT) Disease. Patients who have -registered in the Inherited Neuropathies Consortium Contact Registry will be invited to participate.
The protocol consists of two anonymous surveys. The first large scale survey is designed to identify items that best reflect the issues and symptoms with high impact upon QOL in CMT. A second brief survey focuses on the frequency and impact of muscle cramps on QOL in adult CMT. The surveys will be distributed via an online link to all adult CMT patients self-registered with the RDCRN contact registry. Those who complete the first two surveys will be requested to complete only the second brief survey on muscle cramps again 3 weeks after completing it the first time. Those who complete the brief muscle cramps survey a second time will be requested to complete it again 5 weeks later to assess variability in occurrence of muscle cramps.
The first large scale survey to identify items that best reflect the issues and symptoms with high impact upon QOL in CMT will be sent out in a second wave. This second wave will only contain the QOL survey and not the muscle cramp survey. The QOL survey will be distributed via an online link to three populations: adult CMT patients self-registered with the INC (RDCRN) Contact Registry who had not been registered at the time of the first enrollment period, adult patients who had been registered at the time of the first enrollment period and had received the survey, but had not returned it, and patients who were registered, but were under age 18 at the time of the first enrollment period and have turned 18 by the time of the second enrollment period.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| INC Contact Registry Participants | Adult CMT patients who have self-registered at the Inherited Neuropathies Consortium (INC) Contact Registry, a web-based contact registry developed and supported by the Data Management and Coordinating Center (DMCC) for the Rare Diseases Clinical Research Consortium (RDCRN), located at the University of South Florida. |
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| Measure | Description | Time Frame |
|---|---|---|
| Percentage of participants affected by specific symptoms of CMT. | The percentage of subjects within the sample who have reported experience with the symptom will be calculated. | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Severity of impact of each identified symptom of CMT | The symptoms will be rank ordered with symptoms that affect life severely receiving the highest rank. | 1 year |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with CMT, 18 years or older, who have joined the Inherited Neuropathies Consortium RDCRN Contact Registry.
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| Name | Affiliation | Role |
|---|---|---|
| David Herrmann, MBBCh | University of Rochester | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| RDCRN Data Management and Coordinating Center , Epidemiology Center; University of South Florida | Tampa | Florida | 33612 | United States |
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| ID | Term |
|---|---|
| D002607 | Charcot-Marie-Tooth Disease |
| D015417 | Hereditary Sensory and Motor Neuropathy |
| D009408 | Nerve Compression Syndromes |
| D014076 | Tooth Diseases |
| D000013 | Congenital Abnormalities |
| D030342 | Genetic Diseases, Inborn |
| D020271 | Heredodegenerative Disorders, Nervous System |
| ID | Term |
|---|---|
| D009421 | Nervous System Malformations |
| D009422 | Nervous System Diseases |
| D019636 | Neurodegenerative Diseases |
| D011115 | Polyneuropathies |
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D009057 | Stomatognathic Diseases |
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