Sleep Abnormalities in Rare Genetic Disorders: AS, RTT, and PW

NCT02670694 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 804

Last updated 2016-02-02

No results posted yet for this study

Summary

This study will investigate sleep behavior in subjects with Angelman Syndrome, Rett Syndrome or Prader-Willi Syndrome.

The study will also investigate sleep behavior in healthy siblings of subjects with Angelman Syndrome, Rett Syndrome or Prader-Willi Syndrome. These individuals will serve as control subjects.

The study will use questionnaires designed to identify sleep disorders and how they affect behavior and quality of life.

The principal goals of this study are:

1. To see how common sleep disorders are in individuals with Angelman Syndrome, Rett Syndrome or Prader-Willi Syndrome;
2. To see how sleep disorders affect behavior in these individuals;
3. To see whether sleep disorders and related behavior problems improve or worsen with age;
4. To see how specific disease conditions relate to sleep disorders and how bad the sleep disorders are;
5. To develop new treatment options to improve quality of life and behavior issues; and
6. To evaluate current treatment options to improve sleep problems in these individuals.

Conditions

Sponsors & Collaborators

  • Boston Children's Hospital

    collaborator OTHER
  • University of California, San Diego

    collaborator OTHER
  • Greenwood Genetic Center

    collaborator OTHER
  • University of Florida

    collaborator OTHER
  • Vanderbilt University

    collaborator OTHER
  • University of Kansas Medical Center

    collaborator OTHER
  • University of California, Irvine

    collaborator OTHER
  • University of Alabama at Birmingham

    collaborator OTHER
  • Baylor College of Medicine

    lead OTHER

Principal Investigators

  • Daniel Glaze, MD · Baylor College of Medicine

  • Alan Percy, MD · University of Alabama at Birmingham

  • Sanjeev Kothare, MD · Harvard Medical School, Children's Hospital Boston

Eligibility

Min Age
1 Year
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02670694 on ClinicalTrials.gov