RECRUITING

Genetic and Physical Study of Childhood Nerve and Muscle Disorders

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Background: \- Some nerve and muscle disorders that start early in life (before age 25), like some forms of muscular dystrophy, can run in families. However, the genetic causes of these disorders are not known. Also, doctors do not fully understand how symptoms of these disorders change over time. Researchers want to learn more about genetic nerve and muscle disorders that start in childhood by studying affected people and their family members, as well as healthy volunteers. Objectives: \- To better understand nerve and muscle disorders that start early in life and run in families. Eligibility: * Individuals at least 4 weeks old with childhood-onset muscular and nerve disorders, including those who have a later onset of a disorder that typically has childhood onset. * Affected and unaffected family members of the individuals with muscular and nerve disorders. * Healthy volunteers at least 4 weeks old with no nerve or muscle disorders. Design: * Participants will be screened with a physical exam and medical history. Genetic information will be collected from blood, saliva, cheek swab, or skin samples. Urine samples may also be collected. * Healthy volunteers and unaffected family members will have imaging studies of the muscles. These studies will include magnetic resonance imaging (MRI) and ultrasound scans. Results will be compared with those from the affected participants. * All participants with nerve and muscle disorders will have multiple tests, including the following: * Imaging studies of the muscles, including ultrasound and MRI scans. * Imaging studies of the bones, such as x-rays and DEXA scans. * Heart and lung function tests. * Eye exams. * Nerve and muscle electrical activity tests and biopsies. * Video and photo image collection of affected muscles. * Speech, language, and swallowing evaluation. * Lumbar puncture to collect spinal fluid for study. * Tests of movement, attention, thinking, and coordination. * Participants with nerve and muscle disorders will return to the Clinical Center every year. They will repeat the tests and studies at these visits.

Official Title

Clinical and Molecular Manifestations of Neuromuscular and Neurogenetic Disorders of Childhood

Quick Facts

Study Start:2012-03-20
Study Completion:N/A
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01568658

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:1 Day to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Unaffected family members must be related by blood to a proband enrolled in the study. Biological relations may include first (parent or sibling), second (grandparents, aunts, uncles, half siblings) and third degree relatives (cousins).
  2. 2. Age 4 weeks and older.
  1. 1. Aged 4 weeks and older
  2. 2. Documentation of a personal history of a childhood-onset, hereditary/familial, neurological disorder or later onset of a disease that more commonly has childhood onset. Acceptable documentation includes evaluation through any or all of the following evaluations done prior to enrollment.
  3. 1. Medical history, including family history information
  4. 2. Physical examination
  5. 3. Muscle, nerve, or skin biopsy
  6. 4. Magnetic resonance imaging (MRI)
  7. 5. Electromyography (EMG)
  8. 6. Nerve conduction study (NCS)
  9. 7. Electroencephalogram (EEG)
  10. 8. Muscle ultrasound
  11. 9. Genetic, metabolic, or other laboratory testing such as increased serum Creatine Kinase (CK) and abnormal serum lactate/pyruvate ratio.
  12. 1. Individuals who are unable or unwilling to be examined
  13. 2. Minors who do not hve a parent or guardian able to provide informed consent
  14. 3. Adults seen offsite who are unable to provide their own consent
  15. 1. Aged 4 weeks and older
  16. 2. Documentation of a defined childhood onset neuromuscular and neurogenetic disorders through phase 1 testing.
  17. 1. Individuals who are unable or unwilling to be examined.
  18. 2. Adults who are unable to provide their own consent and who have not previously appointed an individual with Durable Power of Attorney (DPA) or who are unable to appoint a DPA or guardian.
  19. 3. Minors who do not have a parent or guardian able to provide informed consent.
  20. 4. Adults seen offsite who are unable to provide their own consent.

Contacts and Locations

Study Contact

Sandra Donkervoort
CONTACT
(301) 496-0272
sandra.donkervoort@nih.gov
Carsten G Bonnemann, M.D.
CONTACT
(301) 594-5496
bonnemanncg@mail.nih.gov

Principal Investigator

Carsten G Bonnemann, M.D.
PRINCIPAL_INVESTIGATOR
National Institute of Neurological Disorders and Stroke (NINDS)

Study Locations (Sites)

National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
United States

Collaborators and Investigators

Sponsor: National Institute of Neurological Disorders and Stroke (NINDS)

  • Carsten G Bonnemann, M.D., PRINCIPAL_INVESTIGATOR, National Institute of Neurological Disorders and Stroke (NINDS)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2012-03-20
Study Completion DateN/A

Study Record Updates

Study Start Date2012-03-20
Study Completion DateN/A

Terms related to this study

Keywords Provided by Researchers

  • Hereditary Myopathies
  • Neuropathology
  • Muscular Dystrophy
  • Natural History

Additional Relevant MeSH Terms

  • Muscular Dystrophies
  • Muscle Myopathies
  • Hereditary Spastic Paraplegias
  • Inherited Neuropathies
  • Inherited Neuromuscular Conditions