An Analysis of the Symptomatic Domains Most Relevant to Charcot Marie Tooth Neuropathy (CMT) Patients

Sponsor

University of South Florida (Other)

Overall Status

Completed

CT.gov ID

NCT02429947

Collaborator

University of Rochester (Other), National Institute of Neurological Disorders and Stroke (NINDS) (NIH)

411

Enrollment

Location

Duration (Months)

37.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Charcot Marie Tooth Disease (CMT) Hereditary Sensory and Motor Neuropathy Nerve Compression Syndromes Tooth Diseases Congenital Abnormalities Genetic Diseases, Inborn Heredodegenerative Disorders, Nervous System

Detailed Description

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.

Study Design

Study Type:

Observational

Actual Enrollment :

411 participants

Observational Model:

Cohort

Time Perspective:

Cross-Sectional

Official Title:

An Analysis of the Symptomatic Domains Most Relevant to Charcot Marie Tooth Neuropathy (CMT) Patients

Study Start Date :

Jul 1, 2012

Actual Primary Completion Date :

Jun 1, 2013

Actual Study Completion Date :

Jun 1, 2013

Arms and Interventions

Arm	Intervention/Treatment
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.

Outcome Measures

Primary Outcome Measures

Percentage of participants affected by specific symptoms of CMT. [1 year]
The percentage of subjects within the sample who have reported experience with the symptom will be calculated.

Secondary Outcome Measures

Severity of impact of each identified symptom of CMT [1 year]
The symptoms will be rank ordered with symptoms that affect life severely receiving the highest rank.