Effects of Coffee Versus Hibiscus Tea Consumption During Prolonged Sitting on Blood Pressure and Heart Rate

ConditionHypertension
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorKing Saud University

About this trial

Modern lifestyles often involve long periods of sitting, which can increase the risk of heart problems, obesity, and other health issues. Diet also plays a key role in heart health. Coffee and hibiscus tea are two common beverages, but their effects during prolonged sitting are not well understood.

This study will examine how drinking coffee versus hibiscus tea affects blood pressure, heart rate, and heart rate variability in men and women during extended periods of sitting.

Participants (30 in total: 15 women and 15 men) will take part in a randomized crossover study, meaning each person will try both beverages at different times. Data will be collected using questionnaires, body measurements, and devices to measure heart rate, blood pressure, and heart rate variability.

The goal is to better understand how these drinks influence heart health during sedentary behavior.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age between 18 and 35 years.

Normal to elevated blood pressure (systolic <130 mmHg and diastolic <80 mmHg) and normal resting heart rate (60-100 bpm), ensuring selection of healthy adults and minimizing confounding factors.

Generally healthy, without chronic or acute medical conditions, to reduce external influences on study outcomes.

Physically inactive, not meeting current physical activity guidelines, as the study targets sedentary individuals.

Disqualifiers

Known allergy or hypersensitivity to hibiscus or coffee, as participants will consume these beverages during the study.

Current use of medications that could influence blood pressure, heart rate, or heart rate variability, including antihypertensive, chronotropic, or vasoactive drugs.

Any medical condition or health issue that may interfere with safe participation or affect study measurements.

Trial design

Design model

Crossover

Treatments tested in this trial

  • Coffee

    Dietary supplement

    Participants will consume 3 cups of Arabica coffee (Guatemalan origin), providing a total of 400 mg of caffeine. Each cup is prepared with 6% coffee grounds per 100 mL of water, brewed at 90°C for 6 minutes using an electric drip coffee maker, yielding 100.8 mg caffeine per 100 mL. Immediately following coffee consumption, participants will engage in uninterrupted sitting for 3 hours. Blood pressure, heart rate, and other study questionnaires will be measured at baseline (before coffee), 1 hour after coffee intake, and hourly during the 3-hour sitting period.

  • Hibiscus drink

    Dietary supplement

    Participants will consume 3 servings of hibiscus leaves tea per day, each serving containing 1.25 g of dried hibiscus leaves, totaling 3.75 g per session. The tea will be prepared by steeping the leaves in 240 mL of boiling water (100°C) for 10 minutes. Immediately after consuming the hibiscus tea, participants will engage in uninterrupted sitting for 3 hours. Blood pressure, heart rate, and other study questionnaires will be measured at baseline (before tea), 1 hour after tea intake, and hourly during the 3-hour sitting.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Coffee plus prolonged sitting protocolExperimental treatment 1 intervention
Group B: Hibiscus drink plus prolonged sitting protocolExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Systolic and diastolic blood pressure

Systolic and diastolic blood pressure will be assessed using an oscillometric blood pressure monitor (Omron HEM 7124 CP, Omron Healthcare, Illinois, USA). Measurements will be conducted in accordance with the guidelines of the American Heart Association (AHA) and the American College of Cardiology (ACC).

Time frame
Blood pressure will be recorded at five standardized time points: prior to consumption of coffee or hibiscus tea, one hour post-consumption, and following one, two, and three hours of prolonged sitting.
2

Heart Rate

Heart rate will be measured using the Polar V800 system, which consists of a wristwatch and a Bluetooth heart rate sensor. The sensor will be positioned on the participant's chest, just below the pectoral muscles. Participants will remain seated quietly for 10 minutes while continuous heart rate data are recorded according to the manufacturer's instructions. The clearest five-minute segment of the 10-minute recording will be analyzed using Kubios HRV Premium software to assess heart rate (beat/minute)

Time frame
Heart rate measurements will be performed at multiple time points during each visit: prior to beverage consumption, one hour post-consumption, and after one, two, and three hours of prolonged sitting.
3

NN Intervals

NN Intervals will be measured using the Polar V800 system, which consists of a wristwatch and a Bluetooth heart rate sensor. The sensor will be positioned on the participant's chest, just below the pectoral muscles. Participants will remain seated quietly for 10 minutes while continuous heart rate data are recorded according to the manufacturer's instructions. The clearest five-minute segment of the 10-minute recording will be analyzed using Kubios HRV Premium software to assess NN Intervals (milliseconds)

Time frame
NN Intervals measurements will be performed at multiple time points during each visit: prior to beverage consumption, one hour post-consumption, and after one, two, and three hours of prolonged sitting.
4

RMSSD

RMSSD will be measured using the Polar V800 system, which consists of a wristwatch and a Bluetooth heart rate sensor. The sensor will be positioned on the participant's chest, just below the pectoral muscles. Participants will remain seated quietly for 10 minutes while continuous heart rate data are recorded according to the manufacturer's instructions. The clearest five-minute segment of the 10-minute recording will be analyzed using Kubios HRV Premium software to assess RMSSD (milliseconds squared)

Time frame
RMSSD measurements will be performed at multiple time points during each visit: prior to beverage consumption, one hour post-consumption, and after one, two, and three hours of prolonged sitting.

Secondary outcomes

Other outcomes

1

Height

Height (cm) will be measured using an electronic stadiometer (Stadium Scale) with participants standing barefoot in an upright position. Measurements will be performed under standardized conditions, with participants wearing light clothing and no shoes, to ensure accuracy and consistency.

Time frame
One time at baseline
2

Weight

Body weight (kg) will be recorded using a calibrated digital scale (Seca). Measurements will be performed under standardized conditions, with participants wearing light clothing and no shoes, to ensure accuracy and consistency.

Time frame
One time at baseline
3

Body Mass Index

Body mass index (BMI) (kg/m2) will be calculated based on height and weight. Measurements will be performed under standardized conditions, with participants wearing light clothing and no shoes, to ensure accuracy and consistency.

Time frame
One time at baseline
4

Body Fat Percentage

Body fat percentage (%) will be assessed using a bioelectrical impedance analysis device (Tanita MC-980, Japan). Measurements will be performed under standardized conditions, with participants wearing light clothing and no shoes, to ensure accuracy and consistency.

Time frame
One time at baseline

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

King Saud University

Lead sponsor

Princess Nourah Bint Abdulrahman University

Collaborator

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