NCT07002307

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2023

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 19, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 19, 2023

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

May 23, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 3, 2025

Completed
Last Updated

June 15, 2025

Status Verified

June 1, 2025

Enrollment Period

2 days

First QC Date

May 23, 2025

Last Update Submit

June 11, 2025

Conditions

Keywords

CoffeeHoney-sweetened coffeeBlack teaHoney-sweetened black teaGreen TeaHoney-sweetened green teaBlood pressureHeart rateBlood glucose

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 COMPARATOR

Will receive 250 mL of warm water

Other: Warm water at 35 oC

Coffee group

ACTIVE COMPARATOR

Will receive 2.25 g of coffee dissolved in 250 mL of hot water

Other: Coffee

Honey-sweetened coffee group

ACTIVE COMPARATOR

Will receive 2.25 g of coffee plus 20 mL of honey put in 250 mL of hot water

Other: Honey-sweetened coffee

Green tea group

ACTIVE COMPARATOR

Will receive 2 g of green tea infuse in 250 mL of hot water

Other: Green tea

Honey-sweetened green tea group

ACTIVE COMPARATOR

Will receive 2 g of green tea plus 250 mL of honey put in 250 mL of hot water

Other: Honey-sweetened green tea

Black tea group

ACTIVE COMPARATOR

Will receive 2 g of black tea infuse in 250 mL of hot water

Other: Black tea

Honey-sweetened black tea group

ACTIVE COMPARATOR

Will receive 2 g of black tea plus 20 mL of honey put in 250 mL of hot water

Other: Honey-sweetened black tea

Interventions

The placebo for the control group

Control group
CoffeeOTHER

Instant coffee, Nescafé Gold Blend, manufactured by Nestlé Coffee Brand, Nestlé Global

Coffee group

Instant coffee plus raw dark amber honey produced by Apis mellifera adansonii

Honey-sweetened coffee group

Qualitea Natural Green Tea, packed by Qualitea Ceylon (PVT) LTD

Green tea group

Green tea plus honey

Honey-sweetened green tea group

Lipton Yellow Label Black Tea

Black tea group

Black tea plus honey

Honey-sweetened black tea group

Eligibility Criteria

Age18 Years - 26 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Interventions

CoffeeTea

Intervention Hierarchy (Ancestors)

Plant PreparationsBiological ProductsComplex MixturesBeveragesDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Officials

  • Esther O Aluko

    University of Uyo

    PRINCIPAL INVESTIGATOR

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

Locations