No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
100 (estimated)
Sponsor
Efforia, Inc · Industry
Who this trial is looking for
This trial is looking for adults who are dealing with stress and occasional sleep problems. Participants will take two capsules of Neuralli Mood daily for 90 days and complete some surveys about their mood and sleep before and after the trial.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older.
I can give informed consent.
I experience stress or occasional sleep disruption.
I have low mood or anxiety symptoms.
I am willing to take two capsules of Neuralli Mood daily for 90 days.
I can complete online assessments before and after the trial.
I have access to the internet and an email-enabled device.
You may not be able to join if
I am pregnant or nursing.
I am allergic to Neuralli Mood or its ingredients.
I have severe gastrointestinal disease.
I am immunocompromised or on immunosuppressive therapy.
I have a severe mood disorder or acute psychiatric symptoms.
I have a significant sleep disorder that needs medical management.
I have cognitive impairment that affects my ability to consent.
I have had a severe allergic reaction to probiotics.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 …
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.
Trial Locations
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City
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Status
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 an…
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.
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