Menstrual Cycle Hormones and Eating Behavior (FL-84)

Effect of Menstrual Cycle Hormone Changes on Eating Behavior and Nutrient Metabolism

The purpose of this study is to determine if the phase of the menstrual cycle (opposed versus unopposed estrogen phase) affects eating behavior, including types of foods preferred, wanting/desire for specific foods, and perception of hunger.

Study Overview

Status

Completed

Detailed Description

This is an observational study to investigate the effect of endogenous estrogen (E2) and progesterone (P4) levels on eating behavior and energy-yielding nutrient metabolism. Eating behavior will be assessed during a complete menstrual cycle during the first month of the study. Participants will track the follicular and luteal phases of their menstrual cycle using urinary leuteinizing hormone (LH) kits, they will record information about their food intake, eating behaviors, and appetite in their home environments, and they will complete two laboratory test days: one test day scheduled during their follicular phase, and one test day scheduled during their luteal phase.

Study Type

Observational

Enrollment (Actual)

24

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

    • California
      • Davis, California, United States, 95616
        • USDA, ARS, Western Human Nutrition Research Center

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Healthy, premenopausal women.

Description

Inclusion Criteria:

  • Body Mass Index between 20-30 Kg/m2
  • regular menstrual cycles
  • sedentary lifestyle (physical activity not more than 30 minutes per day three times a week)

Exclusion Criteria:

  • Fasting blood sugar greater than 110 mg/dL
  • Systolic Blood Pressure greater than 140 mmHg
  • Diastolic Blood Pressure greater than 90 mmHg
  • Fasting triglycerides greater than 120 mg/dL
  • Documented or self-reported chronic disorders such as arthritis, or other inflammatory diseases
  • Women who are Post-menopausal or Peri-menopausal
  • Pre-menopausal women who are pregnant, uni/multiparous, taking oral contraceptives, or who have menstrual cycles lasting less than 20 days or greater than 45 days, polycystic ovary syndrome (PCOS), amenorrhea, eumenorrhoea, or polymenorrhoea.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eating behavior
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Eating behavior, including types of foods preferred, wanting/desire for specific foods, and perception of hunger will be measured using four questionnaires; Eating inventory: to assess dietary restraint, Stanford Brief Physical Activity Questionnaire, Food craving questionnaire, Eating behavior and attitudes questionnaire
At follicular (day 11) and luteal (day 26) phase of menstrual cycle

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Insulin sensitivity
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
To determine if the phase of the menstrual cycle affects insulin sensitivity, we will measure plasma insulin, glucose and non-esterified fatty acids (NEFA).
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Serum lipid profile changes
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Blood samples will be analyzed for lipids and lipoproteins, including apoproteins A1, B, C-II, C-III, and E.
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Urinary c-peptide
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
The level of urinary C-peptide and creatinine will be measured in a 24-hour urine collection.
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Estradiol
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Estradiol measured in serum in relation to appetite variables
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
progesterone
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Progesterone measured in serum in relation to appetite variables
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Dehydroepiandrosterone (DHEA)
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Dehydroepiandrosterone measured in serum in relation to appetite variables
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Sex Hormone Binding Globulin (SHBG)
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
SHBG measured in serum in relation to appetite variables
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Endocannabinoid profile
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Endocannabinoid profile measured in serum to assess appetite
At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Leptin
Time Frame: At follicular (day 11) and luteal (day 26) phase of menstrual cycle
Leptin measured in serum to assess appetite
At follicular (day 11) and luteal (day 26) phase of menstrual cycle

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Nancy Keim, PhD, USDA, ARS, Western Human Nutrition Research Center

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, 2011

Primary Completion (Actual)

December 1, 2012

Study Completion (Actual)

December 1, 2012

Study Registration Dates

First Submitted

July 26, 2011

First Submitted That Met QC Criteria

July 29, 2011

First Posted (Estimate)

August 2, 2011

Study Record Updates

Last Update Posted (Actual)

December 5, 2017

Last Update Submitted That Met QC Criteria

December 1, 2017

Last Verified

December 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • WHNRC 221594-1

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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