Clinical trial Recruiting at 3 sites Observational Ages 18 to 90

Activia Kefir Use in Real Life

Official title: A Post-launch Study in Spain Assessing Self-perceived Health Benefits and Gut Microbiota Following 2 Weeks Activia Kefir Consumption in Real-world Setting

Run by Danone Global Research & Innovation Center · NCT07790666 · Data updated 2026-11-12

This study checks in real life whether people who use Activia Kefir notice changes in digestive comfort and overall well‑being, and whether it links to the gut microbiome.

Quick facts

Study typeObservational
Ages18 Years to 90 Years
SexAll
Enrollment550 (estimated)
SponsorDanone Global Research & Innovation Center
Industry-sponsored
Drugs / interventionschemotherapy
Locations3 sites (Barcelona and 2 other locations)
StatusRecruiting
StartedAugust 25, 2026
Main results expectedDecember 2026
Study endsDecember 2026
Registry record updatedAugust 31, 2026
Trial IDNCT07790666 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older in Spain who are either regular kefir consumers or willing to start consuming Activia Kefir and complete online questionnaires.

Probably not a fit

Individuals not consuming kefir or not providing online questionnaire data may not benefit from the study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will collect real-world data from adults who either regularly consume or start consuming Activia Kefir. Participants will complete questionnaires about digestive wellbeing, general wellbeing, and related factors, and provide stool samples to explore potential microbiome associations. The study will analyze consumer perceptions and any microbiome signals associated with kefir consumption in Spain. Data will come from self-reported outcomes and biological samples collected across designated Spanish sites. No experimental intervention beyond regular product use is required.

Why it matters

Potential benefit: If successful, findings could help understand how Activia Kefir relates to digestive comfort and quality of life in real-world use.

How similar studies have gone: Observational work in real-world nutrition often identifies associations between dairy probiotic products and digestive well‑being, though mechanisms remain exploratory in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Males and females aged 18 years and older at the time of screening;
2. Willingness to consume Activia Kefir and complete the requested questionnaires;
3. Living in the designated locations in Spain, able to read and write in Spanish;
4. Have a personal electronic device compatible and connectable to internet (i.e., computer, laptop, smartphone) to fill the questionnaires;
5. Signed informed consent.

Exclusion Criteria:

1. People that currently participate in another study with (dairy) investigational or marketed products;
2. Severely immunocompromised individuals (e.g., post-transplant, advanced HIV/AIDS, undergoing chemotherapy);
3. Individuals with known allergies or intolerances to product ingredients. For lactose maldigestion, kefir may improve tolerance, so individuals who are aware of their condition and still wish to participate can be included.

Where it's running

  • Mmr Research Worlwide B.V
    Barcelona, Spain
    Recruiting
  • Mmr Research Worlwide B.V
    Madrid, Spain
    Recruiting
  • Mmr Research Worlwide B.V
    Valencia, Spain
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.