Intra-individual Real Life Effects of Cocoa Flavanols on Blood Pressure and Arterial Stiffness
NCT ID: NCT05446818
Last Updated: 2022-07-07
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
12 participants
INTERVENTIONAL
2019-04-22
2021-02-01
Brief Summary
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Detailed Description
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Aim, hypothesis, objectives: The overall aim of the present pilot study is to evaluate intra-and inter-individual variability of responses to cocoa flavanols in everyday life using the N-of-1 paradigm. It is the hypothesis that cocoa flavanols decrease blood pressure and arterial stiffness in everyday life of healthy individuals. The objectives to investigate the aim are (1) to test the effect of CF using wearable devices repeatedly measuring blood pressure, arterial stiffness, and heart rate in healthy individuals participating in in every days life, (2) to explore intra-and inter-individual variability in responses by repeatedly testing responses in the same individuals, and (3) to test different statistical models taking repeated measurements in the same subject into account.
Methods: In this pilot study, young healthy humans will monitor blood pressure, pulse wave velocity, heart rate, diet, and physical activity on 8 days using a personal and wearable devices. Each subject will undergo the 8 study days; 4 days with cocoa flavanol capsules (CF; containing 750 mg (1500 mg per day)) and 4 days with calorically matched placebo capsules (P; 0 mg cocoa flavanols) taken at the same time in the morning with breakfast and at night before going to bed. The subjects will be randomized to different treatment allocation sequences to allow blinding of volunteers and investigator; either CF-P-CF-P-CF-P-CF-P or P-CF-P-CF-P-CF-P-CF. Blood pressure and heart rate will be measured by a standard upper arm blood pressure cuff and estimated by a fitness wristband and pulse wave velocity via a finger device in 30 min intervals for 3 h starting after morning treatment ingestion followed by hourly intervals until going to bed.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
TRIPLE
Study Groups
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Flavanol first
Subjects will receive over 8 days both cocoa flavanols (CF) and placebo (P) capsules on alternating days. Sequence of this arm is: CF-P-CF-P-CF-P-CF-P
Cocoa flavanol (CF)
2 times per day 750 mg cocoa flavanols (each delivered in 6 CocoaVia capsules)
Placebo (P)
2 times per day 0 mg cocoa flavanols calorically matched control (delivered in 6 identical capsules)
Placebo first
Subjects will receive over 8 days both cocoa flavanols (CF) and placebo (P) capsules on alternating days. Sequence of this arm is: P-CF-P-CF-P-CF-P-CF
Cocoa flavanol (CF)
2 times per day 750 mg cocoa flavanols (each delivered in 6 CocoaVia capsules)
Placebo (P)
2 times per day 0 mg cocoa flavanols calorically matched control (delivered in 6 identical capsules)
Interventions
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Cocoa flavanol (CF)
2 times per day 750 mg cocoa flavanols (each delivered in 6 CocoaVia capsules)
Placebo (P)
2 times per day 0 mg cocoa flavanols calorically matched control (delivered in 6 identical capsules)
Eligibility Criteria
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Inclusion Criteria
* Body mass index \<30 kg/m2
* Age \<45 years
Exclusion Criteria
* Symptoms of acute infection
* Cardiac arrhythmia
* Active malignancy
* Clinical signs or symptoms of cardiovascular disease including:
1. Angina pectoris
2. Shortness of breath
3. Palpitations
4. Syncopes
5. Claudication
* Active vasoactive medication
* Vitamin supplements.
18 Years
45 Years
ALL
Yes
Sponsors
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University of Surrey
OTHER
Responsible Party
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Principal Investigators
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Christian Heiss, MD
Role: PRINCIPAL_INVESTIGATOR
University of Surrey
Locations
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University of Surrey
Guildford, , United Kingdom
Countries
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Other Identifiers
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FER-1819-040
Identifier Type: -
Identifier Source: org_study_id
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