- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02994420
Endocrine and Neural Control of Eating in Women
Steroid Hormones in the Peripheral and Central Control of Eating in Women - Physiological Reactions to Eating in Normal- and Overweight Women
Study Overview
Status
Conditions
Detailed Description
Obesity and the associated severe consequences for health, i.e. cardiovascular diseases or Diabetes Type 2 reach the world-wide level of an epidemic with excessive eating as major cause of this development. Study results of veterinary physiology as well as in women let assume that steroid hormones, such as estrogen or progesterone are highly involved in the regulation of eating behavior and the female body weight. This connection is underpinned with the fact that prevalence of adiposity is increased in women in comparison to men in the United States, Switzerland and further countries. A better understanding of the underlying regulatory mechanisms, which in turn influence the food intake in the gut system through the release of satiety hormones as well as through central regulative mechanisms in the brain, provides important foundation in long-term development of new prophylactic and therapeutic options in reduction and prevention of obesity. This gets even more important, as current therapeutic options - beside bariatric surgery - could only show limited success.
Satiety is a process in the brain that leads to a meal being ended, whereby the ingested food causes a reflexive negative feedback mechanism. This mechanism is both fundamentally and specifically in the acute situation strongly influenced through subjective parameters, e.g. eating desires, socio-cultural factors, current social circumstances and individual relation towards eating. Furthermore, food intake is also influenced by genetic factors, whereas e.g. TaqIA1 allele is known to be associated with obesity. According to current knowledge, regulation takes place on peripheral as well as on central level, whereas not only steroid hormones but also satiety hormones - especially cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1) - are involved on both levels.
The current study aims to examine the connection of steroid hormones, gastrointestinal satiety hormones and neuronal activity in the brain through fMRI. Through the obtained data, the interaction between defined hormone constellations, gastrointestinal satiety hormones and the activation of specific brain areas in obese and normal-weight women should be evaluated. The study design involves the comparison of subjective, hedonic evaluation of different flavoured liquids with different caloric content each through a rating scale as well as objective peripheral (release of CCK and GLP-1) and central (activation of involved brain centres through fMRI) regulation processes in fasted and fed condition of each woman in the two study groups (obese and normal-weighted) in late follicular compared with the luteal phase of ovarian cycle.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Zurich, Switzerland, 8091
- Clinic for Reproductive Endocrinology, University Hospital Zurich
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Physically and psychiatrically healthy women
- Stable body weight (no changes ≥ 5 kg in past year)
- Age 18-35 years
- Regular menses (26-32 d cycles)
- Right-handed
- German language fluency
- Signed informed consent
Exclusion Criteria:
- Life history of eating disorders
- Aversion to the test foods
- Pacemaker or neurostimulator
- Hearing aid
- Surgery to head or heart
- Potential metal parts in body (pacemakers, metal splinters, gun wounds, shrapnel or surgical clips)
- Neurological or psychiatric problems or serious brain injury (such as alcohol or drug abuse, depression, schizophrenia, bipolar disorders, anxiety disorder, claustrophobia, Parkinson's disease, multiple sclerosis, epilepsy)
- High blood pressure, low blood pressure, history of heart disease, irregular heart rate
- Emphysema, chest or respiratory problems (including difficulty breathing through the nose)
- Pregnancy, nursing or pregnancy planned in next three months
- History of gall bladder disease or symptoms (right upper abdominal quadrant pain after meals)
- Polycystic ovary syndrome, as gauged by testosterone levels
- Allergy or sensitivity to lactose
- Allergy to quinine
- Current or previous malignancies
- History of difficult blood sampling
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Lean women
BMI 18-25, weight in kg / height in m2
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Obese women
BMI 30-35, weight in kg / height in m2
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
fMRI responses to food cues
Time Frame: 90 min per study day
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Change in blood oxygen dependent signal (BOLD) in exposure to visual food cues will be measured during a fMRI scan and the difference between responses in the fed condition compared with those in the fasted condition
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90 min per study day
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Change in CCK (satiety hormone) response curve
Time Frame: 30 min per study day
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Blood samples will be collected at 0, 5, 10, 15, 20, 25, 30 min following the ingestion of the meal at each experimental visit, giving a specific curve and analyzed to determine the gut hormone responses.
The results will be compared between fast and fed condition, between obese and normal weight women and depending on ovarian cycle phase.
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30 min per study day
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Change in GLP-1 (satiety hormone) response curve
Time Frame: 30 min per study day
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Blood samples will be collected at 0, 5, 10, 15, 20, 25, 30 min following the ingestion of the meal at each experimental visit, giving a specific curve and analyzed to determine the gut hormone responses.
The results will be compared between fast and fed condition, between obese and normal weight women and depending on ovarian cycle phase.
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30 min per study day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in food preference indicating motivation to purchase food items
Time Frame: 20 min per study day
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The willingness-to-pay task measures the motivation to obtain food on a gLMS scale.
The results will be compared between fast and fed condition, between obese and normal weight women and depending on ovarian cycle phase.
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20 min per study day
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Change in food preference indicating motivation to exert effort
Time Frame: 20 min per study day
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The willingness-to-exert-effort task measures the motivation to obtain food on a gLMS scale.
The results will be compared between fast and fed condition, between obese and normal weight women and depending on ovarian cycle phase.
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20 min per study day
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Dietary intake
Time Frame: 30 min per study day
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Measure of the calorie intake
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30 min per study day
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Hedonic ratings
Time Frame: 20 min per study day
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Subjective ratings of flavor pleasantness will be collected using psychophysical rating scales (gLMS)
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20 min per study day
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Subjective sensory ratings
Time Frame: 20 min per study day
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Subjective ratings of hunger sensation will be collected using psychophysical rating scales (gLMS)
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20 min per study day
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Brigitte Leeners, MD, Clinic for Reproductive Endocrinology, University Hospital Zurich
- Study Chair: Loredana Asarian, Phd, Institute of Veterinary Physiology, Universirty of Zurich
- Study Chair: Philippe Tobler, Prof, Department of Economics, University of Zurich
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015-0525
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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