- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01738399
Coffee and Metabolic Health Outcomes (COMETH)
April 21, 2015 updated by: National University Hospital, Singapore
Influence of Coffee Consumption on Insulin Sensitivity in Overweight and Insulin Resistant Subjects.
The purpose of the study is to investigate the long-term (24 weeks) effects of coffee consumption on insulin sensitivity in insulin resistant individuals.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Coffee is a major source of the phenolic acid chlorogenic acid and a substantial source of trigonelline, niacin, lignans magnesium, and potassium.
Several of these compounds have been shown to improve glucose metabolism in animal models.
Consumption of coffee was inversely associated with the risk of type-2 diabetes in prospective cohort studies across the world.
Consumption of 3 to 4 cups of coffee per day was associated with an approximately 25% lower risk of type-2 diabetes.
However, direct evidence of the efficacy of coffee to reduce blood glucose and insulin resistance parameters in humans from randomized trials is still lacking.
In recent small trials of short duration (up to 6 weeks) coffee consumption increased levels of the insulin-sensitizing hormone adiponectin, but did not significantly improve insulin sensitivity These results suggest that a larger longer-term trial of the effects of coffee consumption on directly measured insulin sensitivity is warranted.
Study Type
Interventional
Enrollment (Actual)
128
Phase
- Not Applicable
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
-
-
-
Singapore, Singapore, 117597
- Saw Swee Hock School of Public Health
-
-
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
35 years to 69 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects classified as being insulin-resistant in the screening visit. Subjects should have a non-diabetic fasting plasma glucose concentration (< 7.0 mM) and a HOMA-IR > 2.2. The HOMA-IR was demonstrated as a reliable indicator of insulin resistance strongly correlated with values obtained by clamp (4). The cut-off value of the HOMA-IR was defined according to data obtained in the Singapore cohort. It corresponds to the 75th percentile of the population. The HOMA-IR cut-off was subsequently revised to ≥ 1.3 to increase recruitment rates.
- Age: ≥ 35 to ≤ 69 years old
- Body mass index : ≥ 22.5 to ≤ 35.4 kg/m2
- Users of at least 1 cups of caffeinated coffee per day who are willing to be randomized to any of the interventions.
- Subjects should be willing to stop consuming caffeinated soft drinks or supplements during the study and to drink coffee with non-dairy creamer.
- Non-smokers (< 1 cigarette per week)
- Participants have been weight stable for at least -8 weeks pre-ceding the screening visit (± 2.5 kgs).
- Chinese, Malay and Indian ethnicity
Exclusion Criteria:
Subjects representing one or more of the following criteria are excluded from participation in the study:
- Any condition/illness that may affect the study outcomes or would make participation potentially harmful such as pregnancy or breastfeeding, diabetes mellitus, heart disease, stroke, hypertension, malabsorption syndromes, GERD, a history of ulcer, clotting or bleeding disorders,allergy to the test beverage, allergy to insulin, according to a detailed medical history.
- Participants who are allergic to foods may be excluded based on the investigator's discretion.
- Participants consume > 2 alcoholic servings/day on a regular basis and > 8 caffeinated servings (based on tea and coffee)/day
- Present drug abuse or use of medications that could interfere with the treatment including bronchodilators, quinolone antibiotics, monoamine oxidase inhibitors, anxiolytics, ranitidine, corticosteroids, growth hormone, anti-hypertensives. These conditions will be screened based on subject reporting. Participants will be asked to bring in their current medications at the time of screening, and these will be checked by the study-staff.
- Subject is taking traditional medications, herbal or dietary supplements that may affect the study outcome in the opinion of the investigators.
- Subject who cannot be expected to comply with the study procedures in the opinion of the investigators.
- Currently participating or having participated in another clinical trial during the last 12 weeks prior to the beginning of this study.
- Premenopausal women with self-reported irregular menstrual cycles or peri-menopausal women (participants who stopped getting their menses for less than 48 weeks ).
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
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Coffee
Subjects take 4 cups of coffee mix per day for 24 weeks
|
|
|
Placebo Comparator: Placebo
Subjects take 4 cups of placebo per day for 24 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in insulin sensitivity when compared to baseline as measured using the euglycemic hyperinsulinemic clamp.
Time Frame: Baseline and 24 weeks
|
Baseline and 24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in fasting plasma glucose concentration from baseline to 12 weeks
Time Frame: Baseline, 12 weeks
|
Baseline, 12 weeks
|
|
Change in fasting plasma glucose concentration from baseline to 24 weeks
Time Frame: Baseline, 24 weeks
|
Baseline, 24 weeks
|
|
Change in fasting plasma total adiponectin concentrations from baseline to 12 weeks
Time Frame: Baseline, 12 weeks
|
Baseline, 12 weeks
|
|
Change in fasting plasma total adiponectin concentrations from baseline to 24 weeks
Time Frame: Baseline, 24 weeks
|
Baseline, 24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Rob M van Dam, Saw Swee Hock School of Public Health, National University of Singapore
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.
General Publications
- Alperet DJ, Rebello SA, Khoo EY, Tay Z, Seah SS, Tai BC, Tai ES, Emady-Azar S, Chou CJ, Darimont C, van Dam RM. The effect of coffee consumption on insulin sensitivity and other biological risk factors for type 2 diabetes: a randomized placebo-controlled trial. Am J Clin Nutr. 2020 Feb 1;111(2):448-458. doi: 10.1093/ajcn/nqz306.
- Alperet DJ, Rebello SA, Khoo EY, Tay Z, Seah SS, Tai BC, Emady-Azar S, Chou CJ, Darimont C, van Dam RM. A randomized placebo-controlled trial of the effect of coffee consumption on insulin sensitivity: Design and baseline characteristics of the Coffee for METabolic Health (COMETH) study. Contemp Clin Trials Commun. 2016 Aug 2;4:105-117. doi: 10.1016/j.conctc.2016.06.013. eCollection 2016 Dec 15.
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
April 1, 2012
Primary Completion (Actual)
December 1, 2014
Study Completion (Actual)
December 1, 2014
Study Registration Dates
First Submitted
November 28, 2012
First Submitted That Met QC Criteria
November 28, 2012
First Posted (Estimate)
November 30, 2012
Study Record Updates
Last Update Posted (Estimate)
April 23, 2015
Last Update Submitted That Met QC Criteria
April 21, 2015
Last Verified
March 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11.09.NRC
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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