Summary

Eligibility
for people ages 20-65 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at Davis, California
Dates
study started
completion

Description

Summary

This study aims to determine the effects of consuming sweet cherry juice on cardiovascular function, glucose regulation, and lipid status in overweight human subjects. The investigators hypothesize that sweet cherry juice consumption will improve metabolic and physiological status in overweight persons compared to a placebo.

Official Title

Cardiometabolic Effects of Sweet Cherry Juice

Details

The investigators will conduct a randomized, cross-over study lasting 14 weeks and including 1 week for screening/enrollment, 1 week baseline assessment, and two intervention periods of 6 weeks each for the cherry juice and placebo interventions. Two test visits, 3 to 7 days apart, will occur before the start of intervention (baseline, or week 0) and then at weeks 6 and 12. Participants will be randomized to consume either the cherry juice or placebo beverage first, and will cross over to the alternate intervention immediately following the end of the first 6 weeks. Test Visit 1 will include measures of blood pressure, vascular tone, liver fat and stiffness, post-prandial metabolic response to the study beverage, cardiovascular activity and function, and nervous system control of cardiovascular activity and tone. Acute effects of study beverages will be measured, as will the chronic effects of study beverage consumption after 6 weeks. At Test Visit 2, participants will take a standard 75 gram oral glucose tolerance test (OGTT). Participants will be equipped with physiological monitoring devices, which will monitor cardiovascular activity and function and nervous system control of cardiovascular activity and tone, and continuously measure blood pressure. A series of cognitive function tasks will be administered, and a mental stress test will be conducted. The Test Visit 1 and 2 will be repeated at week 6 and week 12 following each intervention with cherry juice or the placebo beverage.

Keywords

Obesity, Metabolic Syndrome, cherries, inflammatory disease, chronic stress, Cherry juice

Eligibility

You can join if…

Open to people ages 20-65

  • Men aged 20 - 65 years
  • Post-menopausal women aged 45 - 65 years
  • Body Mass Index ≥25 and <40 kg/m2
  • Systolic blood pressure >120 and <140 mmHg or diastolic blood pressure >80 and <90 mmHg

You CAN'T join if...

  • Diagnosed metabolic disorder
  • Diabetes mellitus
  • Thyroid disease
  • Cardiovascular disease
  • Poly-cystic ovary syndrome
  • Vasoconstrictive diseases (e.g. Raynaud's phenomenon or Raynaud's disease)
  • Digestive disorder (e.g. Crohn's, irritable bowel syndrome, colitis)
  • History of gastrointestinal surgery affecting digestion and/or absorption
  • Use of medications for hypertension, hyperlipidemia, glycemic control, or weight loss
  • Use of medications such as steroids, statins, or non-steroidal anti-inflammatory agents
  • Routine use of over-the-counter medications
  • Weight change >5% in the past 6 months
  • Performing exercise greater than 60 minutes/day
  • Presence of a pacemaker or other internal electronic device controlling rhythm or pacing of heart excludes participant from MindWare procedure
  • Presence of atrial fibrillation or other arrhythmia excludes participant from MindWare procedure

Location

  • USDA, ARS, Western Human Nutrition Research Center
    Davis California 95616 United States

Details

Status
accepting new patients
Start Date
Completion Date
Sponsor
USDA, Western Human Nutrition Research Center
Links
Sign up for this study
ID
NCT03948061
Study Type
Interventional
Participants
About 4 people participating
Last Updated