Stress-buffering and Sleep Disturbance-resilient Effects of a Dual Bifidobacterium Longum Combination Under Short-term Travel

ConditionHealthy
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age25-50
SponsorMin-Tze LIONG

About this trial

This study aims to evaluate the effects of a dual Bifidobacterium longum probiotic formulation (dipro-O and dipro-X) on sleep quality, stress responses, and gut microbiota stability in healthy adults during short-term travel. Using a randomized, double-blind, placebo-controlled design, the study investigates whether probiotic supplementation can enhance sleep resilience, buffer stress, and modulate microbiome and physiological responses under travel-related environmental changes.

Eligibility criteria

Qualifiers

Willing to participate in this study and able to provide written informed consent before any study procedures are initiated.

Able and willing to comply with all study procedures as required by the protocol, including continuous wearable device use, saliva and stool sample collection, and completion of questionnaire assessments.

Willing to accept randomization and group allocation as determined by the study protocol.

Disqualifiers

Known use of antibiotics or systemic corticosteroids within 4 weeks prior to enrollment.

Use of probiotic supplements within 4 weeks prior to enrollment.

Planned use of any probiotic supplements during the study period.

Known history or current presence of major endocrine disorders, active inflammatory bowel disease or other severe gastrointestinal diseases, or severe sleep disorders requiring treatment adjustment.

Trial design

Treatments tested in this trial

  • Placebo
  • Probiotic

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Min-Tze LIONG

Lead sponsor

Universiti Sains Malaysia

Sponsor institution

The Hong Kong Polytechnic University

Collaborator