- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07002307
- Original Trial
The Effect of Honey-sweetened Coffee, Black Tea and Green Tea on Some Physiological Parameters
The Effect of Honey-sweetened Coffee, Black Tea and Green Tea on Blood Pressure, Heart Rate and Blood Glucose
The goal of this clinical trial is to investigate whether a three-day consumption of honey-sweetened black tea, green tea, and coffee will have an effect on blood pressure, heart rate, and blood glucose. The main questions it aims to answer are:
Does honey-sweetened black tea, green tea, and coffee, respectively, have the ability to influence blood pressure, heart rate, or blood glucose level?
Research will compare honey-sweetened black tea, green tea, and coffee to a placebo (warm water) to see if honey-sweetened black tea, green tea, and coffee work to reduce or increase blood pressure, heart rate, or blood glucose.
Participants will:
Take honey-sweetened black tea, green tea, and coffee, OR plain black tea, green tea, and coffee, OR warm water, one cup a day for 3 days The beverages will be taken at the Physiology laboratory, University of Uyo, and the participants will be observed for 60 minutes, during which their blood pressure, heart rate, and blood glucose level will be measured. This procedure will be repeated for the 3 days of study.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Akwa-Ibom
-
Uyo, Akwa-Ibom, Nigeria, 520003
- Physiology laboratory, Physiology Department, Faculty of Basic Medical Sciences, University of Uyo
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Inclusion criteria are as follows:
- Age between 18 and 26
- Non-habitual coffee and tea drinkers who consume coffee, green tea, or black tea 2-5 times in the last two months
- Non-allergic to coffee, green tea, black tea, or honey
- Absence of medication use
- Will refrain from ingesting energy drinks, carbonated beverages, caffeinated beverages, or food for 24 hours before the study and throughout the study periods
- Will not consume anything except water after 11 p.m. during the experimental days Will be available and cooperate throughout the study duration.
Exclusion Criteria:
Exclusion criteria are as follows:
- Presence of cardiovascular disorders, hypertension, or diabetes
- Blood pressure above 120/80 mmHg and random blood glucose above 125 mg/dL
- Alcohol intake
- Smoking
- Habitual coffee or tea drinker
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Control group
Will receive 250 mL of warm water
|
The placebo for the control group
|
|
Active Comparator: Coffee group
Will receive 2.25 g of coffee dissolved in 250 mL of hot water
|
Instant coffee, Nescafé Gold Blend, manufactured by Nestlé Coffee Brand, Nestlé Global
|
|
Active Comparator: Honey-sweetened coffee group
Will receive 2.25 g of coffee plus 20 mL of honey put in 250 mL of hot water
|
Instant coffee plus raw dark amber honey produced by Apis mellifera adansonii
|
|
Active Comparator: Green tea group
Will receive 2 g of green tea infuse in 250 mL of hot water
|
Qualitea Natural Green Tea, packed by Qualitea Ceylon (PVT) LTD
|
|
Active Comparator: Honey-sweetened green tea group
Will receive 2 g of green tea plus 250 mL of honey put in 250 mL of hot water
|
Green tea plus honey
|
|
Active Comparator: Black tea group
Will receive 2 g of black tea infuse in 250 mL of hot water
|
Lipton Yellow Label Black Tea
|
|
Active Comparator: Honey-sweetened black tea group
Will receive 2 g of black tea plus 20 mL of honey put in 250 mL of hot water
|
Black tea plus honey
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Blood pressure
Time Frame: Will be measured before consumption of the beverages and at 15, 30, 45, and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
Will be measured before consumption of the beverages and at 15, 30, 45, and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
|
Heart rate
Time Frame: Will be measured before consumption of the beverages and at 15, 30, 45, and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
Will be measured before consumption of the beverages and at 15, 30, 45, and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
|
Blood glucose
Time Frame: Will be measured before consumption of the beverages and at 30 and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
Will be measured before consumption of the beverages and at 30 and 60 minutes after consumption of the beverages. This procedure will be repeated for 3 consecutive days.
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Age
Time Frame: Will obtained during the eligibility process
|
Will obtained during the eligibility process
|
|
Height
Time Frame: Will be measured on the first day of the experiment before the commencement of the experiment.
|
Will be measured on the first day of the experiment before the commencement of the experiment.
|
|
Body weight
Time Frame: Measurements will be taken over the course of the 3-day study prior to the commencement of the experiment each day.
|
Measurements will be taken over the course of the 3-day study prior to the commencement of the experiment each day.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Esther O Aluko, University of Uyo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Uuthuyo
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Blood Pressure
-
GE HealthcareRecruitingBlood Pressure Measurement | Blood PressureFinland
-
GE HealthcareCompleted
-
Taiwan Biophotonic CorporationCompletedBlood Pressure | Blood Pressure VariabilityTaiwan
-
Université de SherbrookeRecruitingBlood Pressure | Blood Pressure Monitoring, Ambulatory | Blood Pressure, High | Blood Pressure ManagementCanada
-
ROX Medical, Inc.CompletedHypertension | Blood Pressure, High | Blood Pressure, Resistant | Blood Pressure, UncontrolledUnited Kingdom, Netherlands, Belgium
-
DongGuk UniversityActive, not recruitingHypertension | Blood Pressure | Ambulatory Blood Pressure | Home Blood Pressure MeasurementKorea, Republic of
-
Sky LabsSamsung Medical CenterRecruitingHypertension | Blood Pressure | Hypotension | Blood Pressure, High | Blood Pressure, LowKorea, Republic of
-
SE HealthCentre for Aging and Brain Health InnovationCompletedHypertension | Blood Pressure | Hypotension | High Blood Pressure | Low Blood PressureCanada
-
Centre Hospitalier Universitaire VaudoisRecruitingBlood Pressure | Blood Pressure DisordersSwitzerland
-
University of JordanCompletedBlood Pressure | Heart Rate | Airway PressureJordan
Clinical Trials on Warm water at 35 oC
-
Hacettepe UniversityCompletedRheumatoid Arthritis - RheumatismTurkey
-
University of Kansas Medical CenterRecruitingPancreatitis | ERCP SurgeryUnited States
-
Cathay General HospitalCompletedHemorrhoids | Haemorrhoids | Piles | Hemorrhoidal DiseaseTaiwan
-
ARCIM Institute Academic Research in Complementary...Universität TübingenCompletedCardiovascular System | Autonomic Nervous System | Warm FootbathGermany
-
Camillians Saint Mary's Hospital LuodongCompleted
-
Valduce HospitalCompletedUnsedated Colonoscopy | Warm Water | CO2 ColonoscopyItaly
-
German Institute of Human NutritionRecruitingQuality of Life | Stress | Behavior | Psychological WellbeingGermany
-
Cathay General HospitalNot yet recruitingPreoperative Anxiety
-
Trakya UniversityCompletedPituitary Adenoma | SurgeryTurkey (Türkiye)