- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02723682
National Health and Nutrition Examination Survey 24-hour Urine Collection Feasibility Study, 2013
National Health and Nutrition Examination Survey 24-Hour Urine Collection Feasibility Study, 2013
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The 24-hour urine pilot study was conducted March - June 2013 in three NHANES locations. A random half-sample of non-pregnant US adults, aged 20-69 who were examined in the NHANES mobile examination center were selected. Participants received instructions, started and ended the urine collection in a urine study mobile examination center (UMEC), and answered questions about collection. A random half of participants who collected a complete 24-h urine were asked to collect a second 24-h urine. Urinary sodium, potassium, chloride, and creatinine excretion were analyzed.
Participation rates in two other post-examination components, the Physical Activity Monitor and the Dietary Recall, were monitored to determine whether collecting a 24-hour urine had an effect on response rates for the two components.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Maryland
-
Hyattsville, Maryland, United States, 20782
- National Health and Nutrition Examination Survey
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 20-69 year old adults examined in the NHANES mobile examination center
Exclusion Criteria:
- pregnant, unable to respond for themselves
Study Plan
How is the study designed?
Design Details
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Study completion rates - initial collection
Time Frame: 24 hours
|
Completion rate of initial 24-hour urine collection.
|
24 hours
|
Study completion rate - second collection
Time Frame: 24 hours
|
Completion rate of second 24-hour urine collection
|
24 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Response rates for the Physical Activity Monitor
Time Frame: 24-hours
|
Response rates for the Physical Activity Monitor
|
24-hours
|
Response rates for the Phone Follow-up Dietary Recall
Time Frame: 24-hours
|
Response rates for the Phone Follow-up Dietary Recall.
|
24-hours
|
Urine volume for the initial urine collection
Time Frame: 24 hours
|
Urine volume adjusted to 24 hours, initial urine collection
|
24 hours
|
Urine volume for the second urine collection
Time Frame: 24 hours
|
Urine volume adjusted to 24 hours, second urine collection
|
24 hours
|
Urinary sodium excretion for the initial urine collection
Time Frame: 24 hours
|
24-hour urinary sodium excretion, initial urine collection
|
24 hours
|
Urinary sodium excretion for the second urine collection
Time Frame: 24 hours
|
24-hour urinary sodium excretion, second urine collection
|
24 hours
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Kathryn Porter, MD, MS, Centers for Disease Control and Prevention, National Center for Health Statistics, Division of Health and Nutrition Examination Surveys
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2011-17
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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