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Sleep More, Stress Less: 90-Day Trial of Neuralli Mood

RecruitingNA

Sponsor: Efforia, Inc

Conditions: Psychological Stress, Sleep Disturbance, Anxiety Symptoms, Depressive Symptoms, Occupational Burnout

Interventions: Neuralli Mood

Countries: United States

This decentralized, single-arm study evaluates the effects of 90 days of daily Neuralli Mood supplementation on perceived stress, sleep disturbance, mood, anxiety, depressive symptoms, happiness, and occupational burnout in adults experiencing stress or occasional sleep disruption. Participants serve as their own controls, completing validated self-report measures before beginning supplementation and again after the 90-day intervention, with safety and adherence check-ins during the study.

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: Yes

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* Age 18 years or older and able to provide informed consent.
* Generally healthy adult experiencing stress, occasional sleep disruption, low mood, anxiety symptoms, or work-related burnout.
* Willing and able to take two capsules of Neuralli Mood daily for 90 days.
* Willing and able to complete electronic baseline, follow-up, adherence, and safety assessments.
* Has reliable access to the internet and an email-enabled device.

Exclusion Criteria:

* Pregnant or nursing.
* Known allergy or hypersensitivity to Neuralli Mood, probiotics, or any product ingredient.
* Severe or unstable gastrointestinal disease, including a condition for which probiotic use may be inappropriate.
* Immunocompromised status or current immunosuppressive therapy.
* Severe or unstable mood disorder, acute psychiatric symptoms, or a current risk of harm to self or others.
* A clinically significant sleep disorder for which participation or changes in symptoms should be managed by a healthcare professional.
* Cognitive impairment or another condition that prevents informed consent or reliable completion of study procedures.
* History of a severe allergic reaction when the investigator determines probiotic use may present an unacceptable risk.
* Use of a medication or presence of a medical condition for which a healthcare professional advises against probiotic supplementation.
* Any other circumstance that, in the investigator's judgment, makes participation inappropriate or unsafe.

Locations (1)

New York, New York, United States