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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06313580
Other study ID # 22-1055
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date June 2025

Study information

Verified date March 2024
Source University of Alabama, Tuscaloosa
Contact Kristi M Crowe-White, PhD, RD
Phone 205-348-6173
Email kcrowe@ches.ua.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Among food products receiving attention for prebiotic functionality, spices represent a flavorful vehicle for cultivating a healthy gut microbiota. As the required doses of spice-derived polyphenols to elicit prebiotic and systemic metabolic effects are not well-characterized, additional research is warranted. Thus, the investigators propose to use a food-first synbiotic (prebiotic + probiotic) approach to examine alterations in the gut microbiota pre- and post-intervention/placebo and their relationship with systemic cardiometabolic effects mediated by short chain fatty acids (SCFA) and gut-derived metabolites.


Description:

Study will be conducted as a single blind, randomized crossover design with a 4-week arm (placebo or control) followed by a 2-week washout period and another 4-week arm (placebo or control).


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date June 2025
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 69 Years
Eligibility Inclusion Criteria: - post-menopausal women ages 50-69y with a BMI of 18.5 - 34.9 kg/m2 Exclusion Criteria: - Dx - Diagnosis of cardiovascular disease, type 1 or 2 diabetes, liver disease, cancer, endocrine disorders, or inflammatory condition such as rheumatoid arthritis. - GI - History of gastrointestinal surgery, irritable bowel syndrome, intestinal bowel disease, or other gastrointestinal distress such as chronic diarrhea, bulimia, anorexia, or frequent laxative use - Rx or Supplements - Actively taking steroids or antibiotics in the previous two to three months, or currently using tobacco products, > 10% weight loss or gain in the last 6 months, unwilling to stop taking prebiotic/probiotic or fiber supplements - Dietary - Adherence to a high fiber/polyphenol rich diet, have an allergy, aversion, or intolerance to food and spices provided in this study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yogurt with added Spices
Consumption of twice daily yogurt with added spices for four weeks.
Yogurt without added Spices
Consumption of twice daily yogurt without added spices for four weeks.

Locations

Country Name City State
United States The University of Alabama Tuscaloosa Alabama

Sponsors (2)

Lead Sponsor Collaborator
University of Alabama, Tuscaloosa McCormick Science Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Concentration of fecal short chain fatty acids including acetate, proprionate, and butyrate Units - uM pre/post each four-week study arm
Primary Concentration of serum leptin Units - ng/mL pre/post each four-week study arm
Primary Concentration of serum ghrelin (pg/mL) Units - pg/mL pre/post each four-week study arm
Primary Concentration of serum peptide tyrosine tyrosine (PYY) Units - pg/mL pre/post each four-week study arm
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