Acute Effects of Different Protein Sources and Different Glycemic Index on Energy Balance, Glucose Allostasis and Amino Acid Metabolism: a Randomized, 4-condition, Two Cross-over Study in Adults.
FINS
1 other identifier
interventional
48
1 country
1
Brief Summary
The hypothesis is that seafood proteins given in combination with carbohydrates with low GI are superior to seafood proteins in combination with carbohydrates with high GI and meat in combination with both carbohydrates with low and high GI in promoting energy expenditure and satiety. The overall objective of this study is to investigate the acute effects of meals containing fish versus meat proteins on energy balance (thermogenesis, appetite regulating hormones and appetite sensations), markers of glucose allostatis and amino acid metabolism.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2014
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2014
CompletedFirst Submitted
Initial submission to the registry
October 29, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2016
CompletedFirst Posted
Study publicly available on registry
May 12, 2016
CompletedMay 18, 2016
May 1, 2016
1.4 years
October 29, 2014
May 17, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Differences in diet induced thermogenesis between the four test meals
In the following three hours after eating the test meal respiratory gas exchange will be measured 6x25 minutes with 5 minutes breaks in between each measurement. Diet induced thermogenesis (DIT) will be measured by indirect calorimetry using a ventilated hood system. Each measurement will last for 25 minutes of which the last 20 minutes will be used for calculation of energy expenditure.
3 hours
Secondary Outcomes (10)
Satiety
3 hours
Food preferences
3 hours
Glucose
3 hours
Insulin
3 hours
Glucagon
3 hours
- +5 more secondary outcomes
Study Arms (2)
Salmon vs. veal and CHO with low or high GI
EXPERIMENTALIn the first clinical study (Study 1), subjects will eat salmon or veal combined with high or low GI carbohydrates. Each subject will be engaged in each of the following four 1-day test meals: * Meat balls with salmon served with tomato sauce and other accompaniments with low GI * Meat balls with salmon served with tomato sauce and other accompaniments with high GI * Meat balls with veal served with tomato sauce and other accompaniments with low GI * Meat balls with veal served with tomato sauce and other accompaniments with high GI
Cod vs. veal and CHO with low or high GI
EXPERIMENTALIn the second clinical study (Study 2), subjects will eat codfish or veal combined with high or low GI carbohydrates. Each subject will be engaged in each of the following four 1-day test meals: * Meat balls with codfish served with tomato sauce and other accompaniments with low GI * Meat balls with codfish served with tomato sauce and other accompaniments with high GI * Meat balls with veal served with tomato sauce and other accompaniments with low GI * Meat balls with veal served with tomato sauce and other accompaniments with high GI
Interventions
Eligibility Criteria
You may qualify if:
- Healthy men and women
- Between 18 and 50 years of age
- BMI between 25.0 and 30.0 kg×m-2
- Fasting blood glucose \< 5.9 mmol/L (measured at the screenings visit)
- Non-smoker
You may not qualify if:
- Self-reported eating disorders or irregular eating schedule (e.g. skipping breakfast)
- Chronic diseases (e.g. cancer, asthma, back pain, thyroid disease, heart disease, diabetes, neurological disorders, or sleep disorders)
- Use currently or within the previous 3 months of prescription medication that has the potential of affecting body weight or glucose metabolism such as glucocorticoids (but excluding inhaled and topical steroids; bronchodilators are allowed), psychoactive medication, epileptic medication, or weight loss medications (either prescription, over the counter or herbal). Low dose antidepressants are allowed if they, in the judgement of the investigator, do not affect weight or participation to the study protocol. Levothyroxine for treatment of hypothyroidism is allowed if the participant has been on a stable dose for at least 3 months.
- Women who are pregnant, breast-feeding or have intention of becoming pregnant during the study period
- Menopausal women and women with an irregular menstrual cycle
- Food allergies
- Substance abuse
- Vigorous physical activity more than 10 hours/week
- Alcohol intake above the recommendations from the Danish Health and Medicines Authority
- Caffeine intake above 300 mg/day
- Night- or shift work
- Blood donation \<1 month before study commencement and during study period
- Simultaneous participation in other clinical studies
- Inability, physically or mentally, to comply with the procedures required by the study protocol, as evaluated by the study staff
- Subject's general condition contraindicates continuing the study, as judged by the study personnel or the medical expert
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Nutrition, Exercise and Sports
Copenhagen, Frederiksberg, 1958, Denmark
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anne Raben, Prof
Prof at the department of Nutrition, Exercise and Sports
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 29, 2014
First Posted
May 12, 2016
Study Start
August 1, 2014
Primary Completion
January 1, 2016
Study Completion
January 1, 2016
Last Updated
May 18, 2016
Record last verified: 2016-05