Tooth Diseases Clinical Trial
Official title:
An Analysis of the Symptomatic Domains Most Relevant to Charcot Marie Tooth Neuropathy (CMT) Patients
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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