Trials / Recruiting
RecruitingNCT07110896
Study Evaluating the Effect of Humiome® Post LB on Stress, Anxiety, and Cognition in Aging Adults
A Randomized, Placebo-controlled, Double-blind Clinical Study to Evaluate the Effect of Humiome® Post LB on Stress, Anxiety, and Cognition in Aging Adults
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 236 (estimated)
- Sponsor
- dsm-firmenich Switzerland AG · Industry
- Sex
- All
- Age
- 50 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
To assess the effect of 3 months of daily consumption of a postbiotic (inactivated lactic acid bacteria) Humiome® Post LB on stress measured by the Depression Anxiety Stress Scale-21 (DASS-21) adjusted on baseline in study participants when compared to placebo
Detailed description
A double-blinded, randomised and placebo-controlled study will be conducted to assess the effect of 3 months of daily consumption of a postbiotic (inactivated lactic acid bacteria), Humiome® Post LB, on stress measured by the Depression Anxiety Stress Scale-21 (DASS-21) adjusted for baseline in study participants when compared to placebo. The study will be in healthy subjects who are getting older (ageing population) and will measure factors such as stress, sleep, anxiety as well as gut microbiome. The intervention period will be 90 days, and study will include 236 subjects in two arms (active and placebo),
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Humiome Post LB (Postbiotic) | Heat-inactivated lactobacilli with fermented medium (a postbiotic) in 340mg powder format |
| DIETARY_SUPPLEMENT | Placebo | Microcrystalline cellulose, 340mg powder format |
Timeline
- Start date
- 2025-08-01
- Primary completion
- 2026-10-01
- Completion
- 2026-11-01
- First posted
- 2025-08-08
- Last updated
- 2026-03-11
Locations
3 sites across 2 countries: France, Germany
Source: ClinicalTrials.gov record NCT07110896. Inclusion in this directory is not an endorsement.