Appetite and Dietary Intake Across the Menstrual Cycle

NCT ID: NCT06327087

Last Updated: 2024-04-04

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 23 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-06-01
• Study Completion Date: 2025-05-31

Brief Summary

Lay language summary: Women are younger and menstruating about monthly ("pre-menopausal") often have fluctuations in the food they eat ("dietary intake") across the menstrual cycle. However, relationships between food intake and appetite, metabolism, body composition (i.e., the proportion of muscle and fat), physical activity and premenstrual symptoms have not been reported. This study will measure appetite and food intake in laboratory and usual life settings in healthy pre-menopausal women in two hormonally different parts of the menstrual cycle. Data on ovarian hormones, metabolism, body composition, physical activity and premenstrual symptoms will also be collected to assess their potential relationship with food intake.

Detailed Description

Energy balance parameters (dietary intake and energy expenditure) are influenced by gonadal hormones, such as estradiol and progesterone that fluctuate across the menstrual cycle in pre-menopausal women. Dietary intake varies across the menstrual cycle, with higher self-reported energy intake in the luteal phase. However, it is unclear how physiological and behavioral parameters such as appetite, resting metabolic rate, body composition, physical activity, or premenstrual symptoms relate to energy intake fluctuations. Furthermore, only two studies have measured free-living objective dietary intake across the menstrual cycle, neither of which have measured other aspects of energy balance in detail. This study will help address these knowledge gaps by characterizing several aspects of energy balance in both laboratory and free-living settings in healthy pre-menstrual women across the menstrual cycle. Twenty-three women (for complete data on n=18) aged 18-35 without major comorbidities and with normal menstrual cycles will be enrolled in an observational trial. In addition to a baseline visit to measure body composition, participants will undergo two 4.5-hour study visits, one of which will occur in the follicular phase and the other in the luteal phase (as confirmed with multiple low-burden methods including self-reported menstrual cycle history and urinary luteinizing hormone). Participants will be given a two-day run-in diet prior to each study day to ensure energy balance. On each study day visit, participants will undergo a resting metabolic rate test followed by a series of fasting saliva samples quantitatively pooled to measure estradiol and progesterone. Following collection of fasted ratings of appetite, participants will be provided with a standard breakfast meal. Appetite ratings will be repeated 30, 60, 90, 120, 150, and 180 minutes after the meal. Questionnaires related to eating behavior will also be completed during this time. After the 180-minute timepoint, participants will be provided with a buffet-like lunch meal with instructions to eat as much or as little as they would like; this will allow measurement of ad libitum dietary intake at a single meal. To assess free-living ad libitum dietary intake, participants will receive three days of food boxes tailored to their preferences, with uneaten food returned at the end of the three-day period. After each study visit, participants will be asked to record their dietary intake and appetite (three days) and wear and activity monitor (seven days). Differences in outcomes between visits will be assessed using paired samples t-tests and relationships among variables will be assessed via Pearson correlations. This study will provide preliminary evidence of the factors associated with dietary intake fluctuations across the menstrual cycle and provide essential preliminary data that could inform future weight management and health-promotion strategies.

Conditions

Appetitive Behavior; Healthy; Dietary Habits

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Interventions

No intervention

Observational study in the late follicular and mid-luteal phase

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Female sex
• Age: 18 - 35 years
• Nulliparous
• Body mass index (BMI): 18.5 - 24.9 kg/m2
• Premenopausal, with regular menstrual cycle (every 21-38 days, by self-report)
• Sedentary or recreationally active, defined as: <300 minutes per week of voluntary exercise at moderate intensity or greater over the past 12 weeks
• Not currently pregnant or lactating, not planning to become pregnant in the next 12 weeks
• Ability and willingness to fast for 12 hours before each study day visit
• If applicable:

• For people who occasionally (i.e., <1x/day) use cannabis (including cannabidiol-based products): ability and willingness to abstain from cannabis for two days prior to each study day visit, the day of each study visit, and during each ad libitum diet phase.
• For people who use cannabis daily: ability and willingness to continue to use the exact same amount of cannabis as they normally use for two days prior to each study day visit, the day of each study visit, and during each ad libitum diet phase.

Exclusion Criteria

• Current or previous major comorbidities, by self-report, including:

• Cardiovascular diseases
• Diabetes (type 1 or type 2)
• Cancer
• Thyroid diseases
• Human immunodeficiency virus or hepatitis B or C
• Renal diseases
• Hepatic diseases
• Polycystic ovary syndrome
• Uncontrolled/untreated (self-report):

• Hypertension (or measured diastolic blood pressure > 100 mm HG or systolic blood pressure > 160 mm HG)
• Dyslipidemia
• Sleep disorders
• Any other condition that may affect appetite and energy balance
• Currently or in the past six months:

• Use of oral contraceptive pills, or any other hormone-related birth control
• Progestin-releasing intrauterine device
• Use of any hormone therapy/medication ( except medication for thyroid conditions, that has not been altered for >6 months)
• Use of regular medication that may affect appetite, energy balance, or sleep
• Regular use of tobacco or nicotine products
• Starting any new prescription medication within two weeks of the first study day visit or during the study
• If applicable, inability to abstain from supplements or herbal products that may impact sex hormones (e.g., chastetree, phytoestrogens, calcium d glucarate, soy isoflavones, maca, black cohosh, red raspberry, etc.) for two weeks prior to the first study day visit and until the second study day visit and free-living assessments are completed.
• Working night shifts or traveling across more than 2 time zones within two weeks of and throughout the study
• Food intolerances or allergies that cannot be accommodated
• History of surgical procedure for weight loss at any time (e.g. gastroplasty, gastric bypass, gastrectomy or partial gastrectomy, adjustable banding, gastric sleeve); history of extensive bowel resection for other reasons
• Current alcohol or substance abuse (score >1 on the cut down-annoyed-guilty-eye opener [CAGE] questionnaire)
• Current or past history of eating disorders including anorexia nervosa, bulimia, binge eating disorder (self-report or score >20 on the Eating Attitudes Test - 26 [EATS-26] questionnaire)
• Current severe depression or history of severe depression within the previous year, based on score > 30 on Beck Depression Inventory (BDI)
• Weight loss >5kg in past 12 weeks for any reason
• Weight loss of >20 kgs in past 3 years for any reason

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

University of British Columbia

OTHER

Sponsor Role: lead

Responsible Party

Sarah Purcell

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

University of British Columbia - Okanagan

Kelowna, British Columbia, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Sarah A Purcell, PhD

Role: CONTACT

sarah.purcell@ubc.ca

2508079827

Facility Contacts

Sarah Purcell, PhD

Role: primary

sarah.purcell@ubc.ca

2508079827

Other Identifiers

22-00874

Identifier Type: -

Identifier Source: org_study_id