Measurements From Stool to Support Dietary Change

Sponsor
Duke University (Other)
Overall Status
Terminated
CT.gov ID
NCT04037306
Collaborator
(none)
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Study Details

Study Description

Brief Summary

The purpose of the study is to evaluate if daily feedback on food-derived metabolites in stool enhances an individual's ability to make and/or sustain a dietary change.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Butyrate Feedback
  • Behavioral: Fiber Feedback
N/A

Detailed Description

This is a research study to find out how people respond to information about food-derived compounds measured in their stool.

This study will take place over a three-week period. For these three weeks, participants in a medical weight loss program will be asked to collect samples of their stool daily from Monday to Friday, with optional sampling on weekends. We will measure the amount of butyrate, a breakdown product of fiber, in each sample provided and return this measurement by text message. Participants will be randomized into two groups: one group will have new measurements returned the day after providing each stool sample, and another will have their measurements returned all at once, at the end of the study. Both groups will also receive a daily text message report of their fiber intake, based on the foods they ordered at the weight loss facility cafeteria.

The greatest risks of the study include the possibility of infection while sampling stool, possible gastrointestinal discomfort from changes to the diet, and potential loss of confidentiality.

Study Design

Study Type:
Interventional
Actual Enrollment :
7 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Measurements From Stool to Support Dietary Change
Actual Study Start Date :
Jul 30, 2019
Actual Primary Completion Date :
Mar 10, 2020
Actual Study Completion Date :
Mar 10, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Rapid Feedback

Participants received daily feedback on both fiber intake and stool butyrate measurements.

Behavioral: Butyrate Feedback
Measure concentrations of stool butyrate by gas chromatography, returned to participants in summary report.

Behavioral: Fiber Feedback
Estimated fiber consumption from menu records of weight loss facility.

Active Comparator: Delayed Feedback

Participants received daily feedback on fiber intake and one-time feedback on stool butyrate measurements at the end of the study period.

Behavioral: Butyrate Feedback
Measure concentrations of stool butyrate by gas chromatography, returned to participants in summary report.

Behavioral: Fiber Feedback
Estimated fiber consumption from menu records of weight loss facility.

Outcome Measures

Primary Outcome Measures

  1. Change in nutrient intake, as estimated from menu selections [Baseline, Week 2, and Week 3]

    Nutrient intake estimated in grams per day, summed over total menu selections.

Secondary Outcome Measures

  1. Change in butyrate concentration [Baseline, Week 2, and Week 3]

    Butyrate measurements by gas chromatography, reported in mM (millimolar).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • between the ages of 18 and 80

  • must be a client of the DFC (Duke Diet and Fitness Center) weight loss program for at least four continuous weeks.

  • must have a smartphone

Exclusion Criteria:
  • have diagnosis of Crohn's disease

  • have known stricture (narrowing) of the intestine

  • have any past history of intestinal obstruction

Contacts and Locations

Locations

Site City State Country Postal Code
1 Duke University Diet and Fitness Center Durham North Carolina United States 27708

Sponsors and Collaborators

  • Duke University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT04037306
Other Study ID Numbers:
  • Pro00094657
First Posted:
Jul 30, 2019
Last Update Posted:
Sep 2, 2020
Last Verified:
Sep 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Duke University

Study Results

No Results Posted as of Sep 2, 2020