Dose-dependent Identification of Unique Biomarkers

NCT ID: NCT05600348

Last Updated: 2025-01-08

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-01

Study Completion Date

2024-12-01

Brief Summary

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The purpose of the research is to assess the dose-dependent impacts of the consumption of fresh pork on blood-borne metabolites (markers) following the controlled feeding of pork

Detailed Description

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Eligible participants will follow 3 randomly ordered 4-week feeding periods varying only with the consumption of 0, 3 or 6 oz of pork or a 50:50 blend of chicken and beef (6, 3 and 0 oz for respective trials to ensure similar total poultry/meat intake among trials).

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

3 conditions, order randomly allocated
Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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0 oz Pork

Participants receive 0 oz pork and 6 oz 50:50 blend of chicken and beef per day

Group Type EXPERIMENTAL

Pork Consumption

Intervention Type DIETARY_SUPPLEMENT

Feeding of pork is controlled at 0, 3 or 6 oz per day for 4 weeks each in random order.

3 oz Pork

Participants receive 3 oz pork and 3 oz 50:50 blend of chicken and beef per day

Group Type EXPERIMENTAL

Pork Consumption

Intervention Type DIETARY_SUPPLEMENT

Feeding of pork is controlled at 0, 3 or 6 oz per day for 4 weeks each in random order.

6 oz Pork

Participants receive 6 oz pork and 0 oz 50:50 blend of chicken and beef per day

Group Type EXPERIMENTAL

Pork Consumption

Intervention Type DIETARY_SUPPLEMENT

Feeding of pork is controlled at 0, 3 or 6 oz per day for 4 weeks each in random order.

Interventions

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Pork Consumption

Feeding of pork is controlled at 0, 3 or 6 oz per day for 4 weeks each in random order.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* generally healthy (i.e., an absence of diagnosed chronic illnesses and inborn metabolic disorders)
* Age 18-65
* all races
* both sexes
* willingness to comply with the research diet requirements

Exclusion Criteria

* special dietary needs (e.g., vegetarianism, gluten-free, etc.)
* use of medication known to influence metabolism
* smoking
* substance use
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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San Diego State University

OTHER

Sponsor Role lead

Responsible Party

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Shirin Hooshmand

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Shirin Hooshmand, PhD

Role: PRINCIPAL_INVESTIGATOR

San Diego State University

Locations

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School of Exercise and Nutritional Sciences

San Diego, California, United States

Site Status

Countries

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United States

Other Identifiers

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5A949A

Identifier Type: -

Identifier Source: org_study_id

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