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Nutritional Aspects of Rett Syndrome

Primary Purpose

Rett Syndrome

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Metabolic assessment with body composition evaluation
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Rett Syndrome focused on measuring Rett syndrome, neurologic and psychiatric disorders, rare disease

Eligibility Criteria

5 Years - 18 Years (Child, Adult)FemaleAccepts Healthy Volunteers

PROTOCOL ENTRY CRITERIA: Patients aged 5 to 18 with Rett syndrome Able to sleep and awaken alone

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    February 24, 2000
    Last Updated
    June 23, 2005
    Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    Collaborators
    Baylor College of Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00004656
    Brief Title
    Nutritional Aspects of Rett Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 1999
    Overall Recruitment Status
    Completed
    Study Start Date
    May 1993 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    Collaborators
    Baylor College of Medicine

    4. Oversight

    5. Study Description

    Brief Summary
    OBJECTIVES: I. Determine dietary macronutrient intake in children with Rett syndrome and in healthy controls. II. Measure sleeping and awake metabolic rates in various positions, i.e., reclining, sitting, and standing, by whole-room indirect calorimetry and isotope dilution. III. Quantify activity patterns by time-motion studies using 24-hour activity records and 12-hour videotaping. IV. Correlate 24-hour activity patterns with 24-hour heart rate telemetry and short-term oxygen consumption. V. Estimate 24-hour fecal and urinary energy losses. VI. Determine body composition by clinical anthropometry, whole-body potassium counting, and total-body electrical conductance. VII. Calculate apparent energy needs based on measurement of energy intake and expenditure.
    Detailed Description
    PROTOCOL OUTLINE: All participants undergo extensive nutritional and metabolic assessment with body composition evaluation. Studies include macronutrient intake, body fat, lean muscle mass, metabolic rate, and time-action studies; and 24-hour cardiac telemetry. Rett syndrome girls also receive a hemogram and hand x-ray.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rett Syndrome
    Keywords
    Rett syndrome, neurologic and psychiatric disorders, rare disease

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    Metabolic assessment with body composition evaluation

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    5 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    PROTOCOL ENTRY CRITERIA: Patients aged 5 to 18 with Rett syndrome Able to sleep and awaken alone
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kathleen J. Motil
    Organizational Affiliation
    Baylor College of Medicine
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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    Nutritional Aspects of Rett Syndrome

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