Skip to content

Activia Kefir Consumption in Real-world Setting

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07790666
Acronym
KefirSelf
Enrollment
550
Registered
2026-08-27
Start date
2026-08-25
Completion date
2026-12-01
Last updated
2026-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kefir Usual Consumers and New Kefir Consumers

Keywords

Digestive wellbeing, Quality of life, Gut Microbiome

Brief summary

The study aims at generating first real-world insights into how consumers perceive the benefits of consuming Activia Kefir on their digestive wellbeing, overall wellbeing, and to explore its potential effects on the gut microbiome.

Interventions

OTHERCommercialized dairy product consumption and stool samples collection

Consumption of 280 mL (1 bottle) Activia Kefir drinkable per day during the two-weeks study period and collection of 2 stools samples using a collection kit at participant's home (before and after product consumption)

Sponsors

Danone Global Research & Innovation Center
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Stool frequency (number of stools/week, single-item)After 2 weeks of study product consumptionDifference between after consumption and baseline
Digestive symptoms frequency questionnaire (DSFQ, frequency of 4 symptoms: abdominal pain/discomfort, bloating, flatulence, borborygmi)After 2 weeks of study product consumptionDifference between after consumption and baseline
Gastrointestinal (GI)-wellbeing (single-item question)After 2 weeks of study product consumptionDifference between after consumption and baseline
Stool consistency (Bristol stool scale, single-item)After 2 weeks of study product consumptionDifference between after consumption and baseline

Secondary

MeasureTime frameDescription
PROMIS global health questionnaire (10-item, includes questions about emotional state fatigue, pain, general health, quality of life, physical health, mental health, satisfaction social activities, usual activities, and everyday physical activities)After 2 weeks of study product consumptionDifference between after consumption and baseline
WHO wellbeing questionnaire (5-items, includes questions about cheerful/good spirits, calm/relaxed, active/vigorous, feeling fresh/rested, daily life with things that interest me)After 2 weeks of study product consumptionDifference between after consumption and baseline
Perceived resilience (using the 2-item Connor-Davidson Resilience Scale (CD-RISC)-2)After 2 weeks of study product consumptionDifference between after consumption and baseline

Countries

Spain

Contacts

CONTACTDanone Global Research & Innovation Center
register.clinicalresearchnutricia@danone.com+33 (0)1 69 35 70 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026