Reishi Mushroom Extract for Sleep and Stress

This study is looking at how a daily dose of Bristol Fungarium's 1:4 Reishi Mushroom Tincture affects your sleep and stress levels. Researchers want to see if this organic Reishi extract, taken 30 minutes before bed, can improve how long you sleep, how quickly you fall asleep, reduce nighttime awakenings, and make you feel more rested. They also want to see if it can boost your daytime energy and lower your stress. You might be able to join if you are an adult US resident, can read English, and don't have certain health conditions like allergies, liver disease, or chronic illnesses, and are not pregnant or nursing. The study will measure changes in your perceived stress and fatigue after 4-5 weeks, and sleep disturbance after 6-7 weeks.

Study design
This is an interventional study planning to enroll 100 participants. It is a remotely administered, decentralized trial.
What's involved
You would take 1ml of Reishi mushroom extract daily, 30 minutes before bed. The study will assess changes in your stress and fatigue levels after 4-5 weeks, and sleep disturbance after 6-7 weeks.
Compensation
Not stated in the trial record.
Follow-up
Your perceived stress levels will be measured 4-5 weeks after starting the intervention. Your fatigue and sleep disturbance levels will be measured 6-7 weeks after starting the intervention.

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NCT07294482

The Effects on Sleep Quality of 1:4 Reishi Liquid Extract

Recruiting
NAAges 18+InterventionalHealth services
Efforia, Inc
~100 participants
Updated 2025-12-26 on ClinicalTrials.gov
What's tested:Bristol Fungarium's 1:4 Reishi Mushroom Tincture

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Perceived Stress Scale (Past Week Version)
Measured over Change from baseline (Day 1-5) in perceived stress levels at 4-5 weeks after the start of the intervention
+2 more outcomes measured
Sleep
1 sites across 1 states
New York1

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Eligibility criteria

Inclusion

Can read and understand English.
US resident.
Willing and able to follow the requirements of the protocol.

Exclusion

Individuals with Allergies
Pregnant or Nursing Women
Individuals on Anticoagulants
Immunocompromised Individuals
Individuals with Liver Disease
Children and Adolescents
Individuals with Chronic Illnesses
Those with Mental Health Disorders
  • Perceived Stress Scale (Past Week Version)Change from baseline (Day 1-5) in perceived stress levels at 4-5 weeks after the start of the intervention

    The Perceived Stress Scale (Past Week Version) is a modified version of the classic stress assessment tool that evaluates stress levels based on recent experiences within the last week. This scale helps in understanding how various situations have recently affected an individual's feelings and perceived stress levels. By focusing on a shorter time frame, it provides a more immediate assessment of stress, which can be particularly useful for quickly evaluating the effectiveness of stress management strategies or interventions. The tool retains its original structure, ensuring its reliability while making it more relevant for current stress evaluation. Score Range Minimum score: 0 Maximum score: 40 Score Interpretation Higher scores = worse outcome Higher scores indicate greater perceived stress

  • Neuro-QOL Item Bank v1.0 -Fatigue - Short FormChange from baseline (Day 1-5) in fatigue levels at 6-7 weeks after the start of the intervention

    This survey aims to assess the level of fatigue experienced by the participant in the past 7 days. Each question should be answered by selecting one of the five options ranging from 'Never' to 'Always'. Unabbreviated Scale Title Quality of Life in Neurological Disorders (Neuro-QoL™) Item Bank v1.0 - Fatigue - Short Form Score Range Raw score range: Most commonly used short forms: 8-40 T-score range (standardized): Typically \~30 to \~80, mean = 50, SD = 10 Score Interpretation Higher scores = worse outcome Higher scores reflect greater fatigue severity and impact

  • PROMIS Sleep Disturbance ScaleChange from baseline (Day 1-5) in sleep disturbance levels at 6-7 weeks after the start of the intervention

    The PROMIS Sleep Disturbance Scale is a validated and widely used assessment tool developed as part of the Patient-Reported Outcomes Measurement Information System (PROMIS) initiative. It is designed to measure the severity of sleep disturbances and disruptions experienced by individuals. This scale includes a range of questions that assess the frequency and impact of various sleep-related issues, such as difficulty falling asleep, nighttime awakenings, and restless sleep. Healthcare professionals and researchers rely on this scale to better understand and quantify sleep problems in patients, enabling them to tailor interventions and treatment strategies to address sleep-related concerns effectively. Unabbreviated Scale Title Patient-Reported Outcomes Measurement Information System (PROMIS®) Sleep Disturbance Scale Score Range Raw score range: 6-item short form: 6-30 Score Interpretation Higher scores = worse outcome Higher scores indicate greater sleep disturbance (poorer sleep