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Capsaicin Energy Expenditure and Glucose Metabolism (CAPS)

Primary Purpose

Obesity, Insulin Resistance

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Capsaicin
Control
Sponsored by
George Mason University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity focused on measuring capsaicin, resting metabolic rate, glucose

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18-45 years of age females or 18-50 males

    • Generally healthy non-diabetic overweight or obese men and women
    • BMI 23-33 kg/m2
    • Willing to abstain from caffeine and alcohol for 3 days prior to testing
    • Able to provide written consent in English
    • Ability to communicate in English (oral and written)

Exclusion Criteria:

  • BMI < 23 kg/m2 or >33 kg/m2

    • Pregnant or Nursing
    • Taking prescribed or over the counter medication affecting fluid balance or metabolism
    • Suffers from hepatic, renal, pulmonary, endocrine or hematological disease
    • Performs more than 3 hours a week of strenuous exercise
    • Consumes, on average, more than 2 alcoholic beverages per day
    • More than 5 kg of weight change over the past 6 months
    • Claustrophobic
    • Consumes capsaicin foods habitually 3x/week

Sites / Locations

  • George Mason UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Capsaicin

Control

Arm Description

4 tsp of cayenne pepper in a 60g omelette

60 g omelette

Outcomes

Primary Outcome Measures

Postprandial substrate oxidation
The change in substrate oxidation after a meal as measured by the ratio of carbondioxide production and oxygen consumption measured by indirect calorimetry

Secondary Outcome Measures

postprandial energy expenditure
Change in resting energy expenditure after meal consumption as measured by indirect calorimetry

Full Information

First Posted
February 27, 2019
Last Updated
February 28, 2019
Sponsor
George Mason University
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1. Study Identification

Unique Protocol Identification Number
NCT03859583
Brief Title
Capsaicin Energy Expenditure and Glucose Metabolism
Acronym
CAPS
Official Title
Capsaicin Consumption on Resting Energy Expenditure and Glucose Metabolism
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 29, 2018 (Actual)
Primary Completion Date
August 2019 (Anticipated)
Study Completion Date
August 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
George Mason University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to investigate the effects of capsaicin rich foods on resting energy expenditure and substrate oxidation. We plan to recruit 30 healthy lean and overweight individuals age 18-45 (women) and age 18-50 (men) who will undergo two test days in random order. During one day they will receive a breakfast of toast, orange juice and an omelette with 4tsp of cayenne pepper while on the other day they will receive the same breakfast without the cayenne pepper. Metabolic rate and Respiratory quotients is measured for 30 minutes before the meal and for 2 hours after the meal. Capillary glucose levels and heart rate and blood pressure are measured before the meal and every 30 minutes thereafter for 2 hours.
Detailed Description
Participants will be recruited by posters distributed on campus bulletin boards and asked to contact the investigator by phone or e-mail. Participants will complete a screening questionnaire by phone to determine eligibility. Once they pass the screening, they will be invited to the laboratory to sign the consent form, which will be administered by Rafia Virk. They will also be given a demographic survey. The survey will inquire about height, weight, medical conditions, medications and inclusion/exclusion criteria and availability. This survey will be used for screening purposes only and will not contribute to the research data. The survey is included in this application and inclusion and exclusion criteria are outlined. If participants are determined eligible, they will be contacted to set up with two study visits, pre-test instructions will be provided. *For both appointments, participants will arrive to the test location after a 12-hour fast. Appointment 1: Participants will arrive at the Nutrition Assessment Laboratory between 7:00am and 7:30am. Details of the study will be re-iterated and informed consent will be obtained first thing on the morning of the first appointment. Eligibility will then then be confirmed by measuring height and weight and BMI calculation, and a over the counter pregnancy test will be performed on women. Demographic survey and 24-hour dietary recall will be obtained for 2 week days and 1 weekend day. Baseline measurements will then be obtained which include: Waist circumference, body compositition by Dual Energy X-ray Absorptiometry (DXA) scan (performed by Dr. de Jonge or Rafia Virk, who will be trained by Dr. de Jonge). The DXA scan involves lying on a table while wearing lose fitting, comfortable clothing. The scanner uses a low dose x-ray to determine the amount of fat, muscle and bone in your body. After lying down for 30 minutes, a metabolic cart will be used to measure resting energy expenditure by indirect calorimetry. For this procedure, a plastic dome will placed over the participants head that will measure their resting energy expenditure (REE). Baseline REE will then be measured for 30 minutes. After getting a baseline measure participants will consume a standard meal. We will continue to measure resting energy expenditure for 120 minutes. Blood glucose using a glucometer will also be determine before and 2 hours after the standardized meal. The REE measurements will be performed by Ms. Rafia Virk. Ms. Virk will be trained in the use of the metabolic cart by Dr. Lilian de Jonge who has over 20 years experience in the use of indirect calorimetry for the assessment of REE. After this test, the subjects will undergo a capsaicin threshold test. For this test, deionized water with red food coloring will serve as the blank. The testing compound will be cayenne pepper. The target samples, containing very low concentrations of cayenne pepper (0-1mg/g), will also have red food coloring so that they will only be distinguishable to participant by sense of taste rather than taste and sight. There will be nine sets of rows, each with 3 sets of samples. Each set will contain 2 blanks and one target sample. The target sample increase in concentration as the participant moves along the row. The participant will be asked to taste test the samples and pick the target sample out of the three. This appointment will take about 3 hours. The second test day will occur within one week of the first day. The participant will arrive with a 12 hour fast during the first week of the study. They will consume the same standardized meal (provided by Dr. de Jonge) from first appointment but with the addition of capsaicin (cayenne pepper powder form) (4tsp). They will then undergo a metabolic cart test (120 mins). Their blood glucose will also be determined using a glucometer for the following 3 hours post consumption. This appointment will last about 3 hours.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Insulin Resistance
Keywords
capsaicin, resting metabolic rate, glucose

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Capsaicin
Arm Type
Experimental
Arm Description
4 tsp of cayenne pepper in a 60g omelette
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
60 g omelette
Intervention Type
Dietary Supplement
Intervention Name(s)
Capsaicin
Intervention Description
4 tsp of cayenne in a breakfast omelette
Intervention Type
Dietary Supplement
Intervention Name(s)
Control
Intervention Description
breakfast omelette without cayenne pepper
Primary Outcome Measure Information:
Title
Postprandial substrate oxidation
Description
The change in substrate oxidation after a meal as measured by the ratio of carbondioxide production and oxygen consumption measured by indirect calorimetry
Time Frame
3 hours
Secondary Outcome Measure Information:
Title
postprandial energy expenditure
Description
Change in resting energy expenditure after meal consumption as measured by indirect calorimetry
Time Frame
3 hrs

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18-45 years of age females or 18-50 males Generally healthy non-diabetic overweight or obese men and women BMI 23-33 kg/m2 Willing to abstain from caffeine and alcohol for 3 days prior to testing Able to provide written consent in English Ability to communicate in English (oral and written) Exclusion Criteria: BMI < 23 kg/m2 or >33 kg/m2 Pregnant or Nursing Taking prescribed or over the counter medication affecting fluid balance or metabolism Suffers from hepatic, renal, pulmonary, endocrine or hematological disease Performs more than 3 hours a week of strenuous exercise Consumes, on average, more than 2 alcoholic beverages per day More than 5 kg of weight change over the past 6 months Claustrophobic Consumes capsaicin foods habitually 3x/week
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elisabeth de Jonge, PhD
Phone
7039935153
Email
edejonge@gmu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Rafia VIrk, BSc
Phone
7039935153
Email
rvirk@gmu.edu
Facility Information:
Facility Name
George Mason University
City
Fairfax
State/Province
Virginia
ZIP/Postal Code
22030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elisabeth de Jonge
Phone
703-993-5153
Email
edejonge@gmu.edu
First Name & Middle Initial & Last Name & Degree
Rafia Virk
Phone
7039935153
Email
rvirk@gmu.edu

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Capsaicin Energy Expenditure and Glucose Metabolism

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