Antioxidant Capacity and Vitamin A Profile in Young Adults Who Consume a Snack Bar Made From Tropical Fruits Treated With UV-C
Primary Purpose
Nutritional and Metabolic Disease
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
No Intervention
Pineapple snack bar
Mango snack bar
Sponsored by
About this trial
This is an interventional treatment trial for Nutritional and Metabolic Disease focused on measuring antioxidant capacity
Eligibility Criteria
Inclusion Criteria:
- Young adults of 18 years of age or older,
- Healthy in appearance
Exclusion Criteria:
- People in current medical treatment
- Used antibiotics in past 15 days
- Have presented infectious symptoms on previous days
- Smokers
- Narcotic consumers
- Women in use of hormonal treatment
- Contraceptives or pregnancy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
No Intervention
Intervention pineapple
Intervention mango
Arm Description
This group did not have an intervention
Daily consumption of 30 g of pineapple snack bar for 4 weeks.
Daily consumption of 30 g of mango snack bar for 4 weeks.
Outcomes
Primary Outcome Measures
Change Oxygen Radical Absorbance Capacity Assay (Antioxidant Capacity)
From baseline and thirty days post treatment
Change Trolox Equivalent Antioxidant Capacity (Antioxidant Capacity)
From baseline and thirty days post treatment
Change Serum Retinol Determination
From baseline and thirty days post treatment
Change Serum pro-VA carotenoids
From baseline and thirty days post treatment
Secondary Outcome Measures
Change Serum total polyphenols determination
From baseline and thirty days post treatment
Change Serum cholesterol determination
From baseline and thirty days post treatment
Change Serum Triacylglycerides determination
From baseline and thirty days post treatment
Change Serum high density lipoprotein cholesterol
From baseline and thirty days post treatment
Change Body Mass Index
From baseline and thirty days post treatment
Change Body composition by fat-free mass index
From baseline and thirty days post treatment
Change Body composition by fat mass index
From baseline and thirty days post treatment
24-hour dietary recall
From baseline and thirty days post treatment
Full Information
NCT ID
NCT03520725
First Posted
February 23, 2018
Last Updated
April 27, 2018
Sponsor
Centro de Investigación en Alimentación y Desarrollo A.C.
Collaborators
Universidad de Sonora
1. Study Identification
Unique Protocol Identification Number
NCT03520725
Brief Title
Antioxidant Capacity and Vitamin A Profile in Young Adults Who Consume a Snack Bar Made From Tropical Fruits Treated With UV-C
Official Title
Antioxidant Capacity and Vitamin A Profile in Young Adults Who Consume a Snack Bar Made From Tropical Fruits Treated With UV-C.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
December 2016 (undefined)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
April 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro de Investigación en Alimentación y Desarrollo A.C.
Collaborators
Universidad de Sonora
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objective of the present study was to evaluate the impact of a snack bar on some health indicators associated with diet (plasma antioxidant capacity, lipid profile, vitamin A profile (retinol and carotenoids)) and on the nutritional status (impact on energy and nutrients consumed) in a group of upper level students.
Detailed Description
A blind randomized controlled clinical study of healthy adults, which was carried out with the approval of the ethics committee of the Centro de Investigación en Alimentación y Desarrollo, A.C. (CIAD, A.C.) with registration CE/001/2017. The intervention was carried out in a public university in Mexico from January to April 2017. Each subject signed an informed consent form. This study lasted 30 days (4 weeks), where each participant consumed daily a snack bar irradiated with UV-C. The participants were personally interviewed by the research team with a structured selection questionnaire. Thirty subjects who met the inclusion criteria were recruited, 15 of them men and 15 women. Through a simple randomization process, the participants were assigned in 3 groups of 10 people each with 5 women and 5 men, subsequently treatments (without treatment, pineapple snack bar, or mango snack bar) were randomly assigned. The outcomes between groups were analyzed with one way ANOVA, with a P-value of 0.05 or less when there was statistical significance, using statistical software. The participants, and the laboratory technicians were blinded to the treatment assignments until the conclusion of the trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nutritional and Metabolic Disease
Keywords
antioxidant capacity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
No Intervention
Arm Type
Experimental
Arm Description
This group did not have an intervention
Arm Title
Intervention pineapple
Arm Type
Experimental
Arm Description
Daily consumption of 30 g of pineapple snack bar for 4 weeks.
Arm Title
Intervention mango
Arm Type
Experimental
Arm Description
Daily consumption of 30 g of mango snack bar for 4 weeks.
Intervention Type
Other
Intervention Name(s)
No Intervention
Intervention Description
This gruop did not have an intervention
Intervention Type
Dietary Supplement
Intervention Name(s)
Pineapple snack bar
Intervention Description
30 g daily of pineapple snack bar
Intervention Type
Dietary Supplement
Intervention Name(s)
Mango snack bar
Intervention Description
30 g daily of mango snack bar
Primary Outcome Measure Information:
Title
Change Oxygen Radical Absorbance Capacity Assay (Antioxidant Capacity)
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Trolox Equivalent Antioxidant Capacity (Antioxidant Capacity)
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Serum Retinol Determination
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Serum pro-VA carotenoids
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Secondary Outcome Measure Information:
Title
Change Serum total polyphenols determination
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Serum cholesterol determination
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Serum Triacylglycerides determination
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Serum high density lipoprotein cholesterol
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Body Mass Index
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Body composition by fat-free mass index
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
Change Body composition by fat mass index
Description
From baseline and thirty days post treatment
Time Frame
Change from baseline at thirty days
Title
24-hour dietary recall
Description
From baseline and thirty days post treatment
Time Frame
Baseline and thirty days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Young adults of 18 years of age or older,
Healthy in appearance
Exclusion Criteria:
People in current medical treatment
Used antibiotics in past 15 days
Have presented infectious symptoms on previous days
Smokers
Narcotic consumers
Women in use of hormonal treatment
Contraceptives or pregnancy
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The data base will not be shared, each collaborator will participate verifying the handling of the samples and the process of analysing the results in a blinded manner.
Learn more about this trial
Antioxidant Capacity and Vitamin A Profile in Young Adults Who Consume a Snack Bar Made From Tropical Fruits Treated With UV-C
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