Pea protein power: can a vegetarian diet change how your body uses plant protein?
NCT ID NCT07521189
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how well people digest and use protein from peas, comparing young and older adults who are either vegetarians or omnivores. Researchers will measure protein absorption after a pea-based meal using special tracers. The goal is to understand if age or diet affects how the body handles plant protein, which could help improve nutrition for older adults.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- pea protein
- What this could lead to
- If successful, this study could help design better nutritional strategies for older adults who need more protein, especially those on plant-based diets.
- What could go wrong
- This is an early-stage observational study with only 48 participants, so results may not apply to everyone. It measures digestion markers, not health outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Normal weight or overweight (18 \< BMI \< 30 kg·m-²) * Male or female * Aged 18-23 years (young groups) or 65-75 years (older groups) * Following an omnivorous diet (regular consumption of meat products, with meat intake \> 3 times/week and \> 70% of protein intake from animal sources) or vegetarian diet (exclusion of meat and fish/seafood, with \> 70% of protein intake from plant sources) * In good general health (WHO = 0) * Affiliated with a social security system * Free and informed consent, provided in writing after receiving the information required by the Public Health Code Exclusion Criteria: * Adults under legal protection or unable to give informed consent (e.g., under guardianship, trusteeship, or legal protection) * Any known food allergy * Positive serology for HBsAg, anti-HBc, HCV, or HIV * Anemia: hemoglobin level \< 13 g/dL in men and \< 12 g/dL in women * Pregnant women or those who may be pregnant (based on a positive urine pregnancy test at inclusion) * Excessive alcohol consumption (\> 2 drinks/day). Harmful alcohol use will be assessed by the investigator at inclusion. * Hypertension, diabetes, gastrointestinal, liver or kidney diseases, or severe heart disease. These conditions will be assessed by the investigator based on standard clinical evaluation and participants' self-reports at inclusion. * Hypertension: significant arterial hypertension according to the investigator, or systolic blood pressure ≥ 140 mmHg and/or diastolic blood pressure ≥ 90 mmHg at inclusion. * Diabetes: type 1 or type 2 diabetes, or fasting blood glucose \> 1.25 g/L. * Gastrointestinal disease: clinically significant gastrointestinal disorders (bleeding, vomiting, constipation/diarrhea grade \> 1) as judged by the investigator, any inflammatory bowel disease, or acute gastroenteritis in the month prior to the intervention. * Liver disease: any significant hepatic disorder according to the investigator, or ASAT/ALAT \> 2.5 times the upper normal limit. * High-level athletes (\> 8 hours of training per week) * Blood donation within 8 weeks prior to study start * Absence of free, informed, written consent after receiving the information required by the Public Health Code * Not affiliated with a social security system
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre de Recherche sur Volontaire, Hopital Avicenne (AP-HP)
RECRUITINGBobigny, France
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