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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05885750
Other study ID # Newplant
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 5, 2023
Est. completion date December 31, 2024

Study information

Verified date June 2023
Source University of Turku
Contact Veera Houttu, PhD
Phone +358504627287
Email veera.houttu@utu.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is observed that replacing meat with protein-rich plant-based food products are associated with lower mortality and obesity prevention. Sources of plant proteins typically undergo several processing and refinement procedures to improve the taste and digestibility of plant-based food products. These procedures alter the chemical composition, which can impact the nutritional quality of the processed food. It is not known what is the impact of processed products on human metabolism and intestinal microbiota. Therefore, the impact of a set of plant-based protein-rich food products with varying degree of processing on the composition and function of human gut microbiome and metabolism will be assessed in a clinical intervention


Description:

Plant-based diets are known to have beneficial effects on both the environment and human health. Replacing animal protein with plant protein reduces overall mortality risk, and replacing meat with legumes and other sources of plant protein can lower the risk of chronic diseases such as type 2 diabetes and cardiovascular disease. However, the benefits of plant protein products is not evident. In order to make plant protein products more palatable and digestible, plant raw materials may go through several processing and refinement procedures. Typically, during these phases, carbohydrate fractions (e.g. dietary fiber) are removed from the plant material, which results in the loss of micronutrients as well as secondary plant metabolites with potentially health effects (e.g. polyphenolic compounds). Salt and various fats are added to some products, which can reduce the nutritional quality of the product. Subsequently, not all plant-based protein-rich foods are automatically healthy as there may be significant differences in the nutritional quality of the processed products, depending on the food processing utilized. Only little research information is available on the effects of processed plant protein products on human metabolism and intestinal microbiota. Therefore, this cross-over clinical intervention will be conducted with 38 healthy participants to investigate the impact of a set of plant-based protein-rich food products with varying degree of processing on the composition and function of human gut microbiome and metabolism will be assessed in a clinical intervention.


Recruitment information / eligibility

Status Recruiting
Enrollment 38
Est. completion date December 31, 2024
Est. primary completion date September 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Willingness to participate - 18-65-years olf - BMI 18.5-27 kg/m2 Exclusion Criteria: - Chronic disease with continuous medication - Antibiotic use in the past 6 months - Active smoker - Gluten-free or vegan diet - Pregnancy, lactation - Abnormal thyroid, liver, or kidney function - Low hemoglobin

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Unprocessed
Participants will consume unprocessed or minimally processed commercially available plant-based protein-rich foods as meat replacement in their normal diet for one week.
Mildly processed
Participants will consume mildly processed commercially available plant-based protein-rich foods as meat replacement in their normal diet for one week.
Heavily refined
Participants will consume heavily refined processed commercially available plant-based protein-rich foods as meat replacement in their normal diet for one week.

Locations

Country Name City State
Finland Food Sciences Unit, Department of Life Technologies, Faculty of Technology, University of Turku Turku

Sponsors (1)

Lead Sponsor Collaborator
University of Turku

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Metabolomics The changes in metabolism evoked by the interventions one week between the start and end of each intervention
Primary Transcriptomics The changes in endogenous gene expression on RNA level one week between the start and end of each intervention
Primary Metagenomics The alterations in the composition of gut microbiota one week between the start and end of each intervention
Primary Inflammation status by inflammatory cytokines The changes in inflammatory cytokines one week between the start and end of each intervention
Primary Inflammation status by high-sensitive CRP The changes in high-sensitive CRP by clinical biochemistry analysis one week between the start and end of each intervention
Secondary Glucose homeostasis Fasting plasma glucose and insulin concentrations by clinical biochemistry analyses one week between the start and end of each intervention
Secondary Lipid homeostasis Cholesterol and triglyceride concentrations by clinical biochemistry analyses one week between the start and end of each intervention
Secondary Body weight Body weight in kilograms measured by standard weight scale five weeks (baseline and at the end of the complete study / after three interventions and 2 wash-outs)
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