Can a protein powder with creatine and fiber boost everyday Well-Being?
NCT ID NCT07827014
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers are testing a daily multi-ingredient protein powder in healthy adults aged 21 to 65. About 50 participants receive either a vanilla or chocolate version for 15 days and answer questionnaires at home. The study tracks tolerability, overall liking, and changes in self-reported global health and cognitive function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A multi-ingredient protein powder combining fermented yeast protein, collagen peptides, creatine, and prebiotic fiber, in vanilla or chocolate flavor
- What this could lead to
- If the formula proves tolerable and well liked, it could support further study of protein powders that combine creatine and fiber for everyday wellness.
- What could go wrong
- This is a small, short pilot with no placebo group, so any well-being changes could reflect expectation or daily routine rather than the formula. Supplements can also cause bloating or stomach upset.
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 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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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21 to 65 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: * Adults aged 21-65 years, inclusive * Generally healthy, as determined by self-reported medical history and investigator judgment * Body mass index 18.5-34.9 kg/m² (as operationally verified) * Willing and able to consume the test product once daily for 15 days and to complete scheduled questionnaires * Can read and write English. * Provide voluntary, written, informed consent to participate in the study. * Agree to provide a valid cell phone number and are willing to receive communications through text. * Willing to complete questionnaires, records, and diaries associated with the study. * Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly Exclusion Criteria: * Known allergy or intolerance to any study-product component, including yeast-derived protein, bovine collagen, creatine, the prebiotic fiber blend, allulose, or Reb M. * Women who are pregnant, breastfeeding, or planning to become pregnant or start breastfeeding during the trial * Clinically significant gastrointestinal disorder that could confound tolerability assessment (e.g., inflammatory bowel disease, symptomatic irritable bowel syndrome, prior major GI surgery), per investigator judgment * Known renal impairment or condition for which supplemental creatine is not advised * Serious or unstable medical condition, or any condition that in the investigator's judgment would compromise participant safety or data integrity * Participation in another interventional study within 30 days prior to enrollment * Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, cancer * Having had a significant cardiovascular event in the past 6 months * Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines * On immunosuppressive therapy * Having had surgery within the past 6 weeks or upcoming planned surgery in the next few months * Adults lacking capacity to consent
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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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Qualia Life Sciences
RECRUITINGCarlsbad, California, 92008, United States
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