Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
128 participants
INTERVENTIONAL
2012-04-30
2014-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Coffee
Subjects take 4 cups of coffee mix per day for 24 weeks
Coffee
Placebo
Subjects take 4 cups of placebo per day for 24 weeks
Placebo
Interventions
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Coffee
Placebo
Eligibility Criteria
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Inclusion Criteria
* 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
* 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 ).
35 Years
69 Years
ALL
No
Sponsors
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Société des Produits Nestlé (SPN)
INDUSTRY
National University Hospital, Singapore
OTHER
Responsible Party
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Principal Investigators
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Rob M van Dam
Role: PRINCIPAL_INVESTIGATOR
Saw Swee Hock School of Public Health, National University of Singapore
Locations
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Saw Swee Hock School of Public Health
Singapore, Singapore, Singapore
Saw Swee Hock School of Public Health
Singapore, , Singapore
Countries
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References
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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.
Other Identifiers
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11.09.NRC
Identifier Type: -
Identifier Source: org_study_id
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