Grape Seed Extract for Heart Rate Recovery in Young Individuals
600 mg grape seed extract
+ 600 mg Starch
Prevention Study
Summary
Study start date: October 3, 2024
Actual date on which the first participant was enrolled.The study investigates whether grape seed extract (GSE) can help improve how quickly the heart rate returns to normal after exercise in young people. The main idea is that certain body responses might slow down this process and that taking GSE could make it faster. By focusing on young individuals, the research aims to find new ways to support heart health and recovery after physical activities, potentially offering a simple supplement-based approach to enhance cardiovascular recovery. Participants in the study take part in a controlled exercise test using a stationary bike and a handgrip exercise device. They are given either grape seed extract or a placebo, with both treatments appearing identical to ensure unbiased results. Heart rate recovery is carefully tracked every few seconds after the exercise to see how quickly it returns to resting levels. The results between the grape seed extract and placebo are compared to determine the extract's effectiveness. Participants are monitored closely to ensure safety and accuracy throughout the trials.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.12 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Male
Biological sex of participants that are eligible to enroll.From 18 to 30 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
California Baptist University
Riverside, United StatesOpen California Baptist University in Google Maps