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
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
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
NCT ID
NCT00004656
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
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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