Purpose

A natural history study to understand the expected progression of disease in patients with confirmed mutations in the VCP gene over 1 year.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Genetically confirmed mutation in the VCP gene - Age ≥18 years - Willing and able to provide informed consent and follow all study procedures

Exclusion Criteria

  • Participation in an interventional clinical trial - Any concomitant illness or comorbid condition that would interfere with a patient's ability to complete study procedures safely at the discretion of the site PI.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Recruiting Locations

Nationwide Children's Hospital
Columbus, Ohio 43205
Contact:
Lindsay Alfano
614-722-6881
nmdtrialinfo@nationwidechildrens.org

More Details

NCT ID
NCT04823143
Status
Recruiting
Sponsor
Nationwide Children's Hospital

Study Contact

Lindsay Alfano
6147226881
nmdtrialinfo@nationwidechildrens.org

Detailed Description

This is a single site, prospective natural history study to evaluate the utility of strength, functional, and patient reported outcomes in quantifying disease progression over 1 year in patients with mutations in the VCP gene. Patients will complete a remote and onsite visits at baseline, a remote visit at 6 months, and then a final remote and onsite visit at 12 months. All strength, functional, and patient reported measures will be completed at each visit to assess reliability, consistency of results across testing environments, and sensitivity to change over time. Additionally, patients may opt in to provide blood, serum, and urine samples for biobanking.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.