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

A 24-hour urine pilot study was conducted as part of the 2013 NHANES to test the feasibility of implementing a 24-hour urine collection as part of NHANES in 2014.

Study Overview

Status

Completed

Conditions

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

Observational

Enrollment (Actual)

282

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Maryland
      • Hyattsville, Maryland, United States, 20782
        • National Health and Nutrition Examination Survey

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.

Eligibility Criteria

Ages Eligible for Study

20 years to 69 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

NHANES participants aged 20-69 years who were examined in the mobile examination center.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

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

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 Major Dates

Study Start

March 1, 2013

Primary Completion (Actual)

June 1, 2013

Study Completion (Actual)

June 1, 2013

Study Registration Dates

First Submitted

March 8, 2016

First Submitted That Met QC Criteria

March 24, 2016

First Posted (Estimate)

March 30, 2016

Study Record Updates

Last Update Posted (Estimate)

March 30, 2016

Last Update Submitted That Met QC Criteria

March 24, 2016

Last Verified

March 1, 2016

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)?

No

IPD Plan Description

The NHANES 24-hour urine pilot study data set can be made available through the National Center for Health Statistics Research Data Center by submitting a research proposal at http://www.cdc.gov/rdc/.

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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