The Effect of Honey-sweetened Coffee, Black Tea and Green Tea on Some Physiological Parameters
1 other identifier
interventional
70
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2023
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
October 17, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 19, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
October 19, 2023
CompletedFirst Submitted
Initial submission to the registry
May 23, 2025
CompletedFirst Posted
Study publicly available on registry
June 3, 2025
CompletedJune 15, 2025
June 1, 2025
2 days
May 23, 2025
June 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Blood pressure
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
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
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 Outcomes (3)
Age
Will obtained during the eligibility process
Height
Will be measured on the first day of the experiment before the commencement of the experiment.
Body weight
Measurements will be taken over the course of the 3-day study prior to the commencement of the experiment each day.
Study Arms (7)
Control group
PLACEBO COMPARATORWill receive 250 mL of warm water
Coffee group
ACTIVE COMPARATORWill receive 2.25 g of coffee dissolved in 250 mL of hot water
Honey-sweetened coffee group
ACTIVE COMPARATORWill receive 2.25 g of coffee plus 20 mL of honey put in 250 mL of hot water
Green tea group
ACTIVE COMPARATORWill receive 2 g of green tea infuse in 250 mL of hot water
Honey-sweetened green tea group
ACTIVE COMPARATORWill receive 2 g of green tea plus 250 mL of honey put in 250 mL of hot water
Black tea group
ACTIVE COMPARATORWill receive 2 g of black tea infuse in 250 mL of hot water
Honey-sweetened black tea group
ACTIVE COMPARATORWill receive 2 g of black tea plus 20 mL of honey put in 250 mL of hot water
Interventions
Instant coffee, Nescafé Gold Blend, manufactured by Nestlé Coffee Brand, Nestlé Global
Instant coffee plus raw dark amber honey produced by Apis mellifera adansonii
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Physiology laboratory, Physiology Department, Faculty of Basic Medical Sciences, University of Uyo
Uyo, Akwa Ibom State, 520003, Nigeria
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Esther O Aluko
University of Uyo
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator (PI)
Study Record Dates
First Submitted
May 23, 2025
First Posted
June 3, 2025
Study Start
October 17, 2023
Primary Completion
October 19, 2023
Study Completion
October 19, 2023
Last Updated
June 15, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share