Evaluating SleepWhale Drops for Rest & Resilience

This study is testing SleepWhale Natural Sleep Drops, a non-melatonin supplement with broad spectrum hemp extract, L-Theanine, Magnesium, Camomile, and Lion's Mane. Researchers want to see if these drops can improve your sleep quality and how you feel during the day. You might be able to join if you live in the US, can read English, and are willing to follow the study rules. However, you cannot participate if you have allergies to the ingredients, take sleep medication, have stomach problems, skin conditions, or are prone to headaches. The study will consider SleepWhale successful if participants report better sleep, less daytime sleepiness, and reduced fatigue after 4 weeks. The current status of this study is unclear.

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 SleepWhale Drops nightly for 30 days and complete weekly check-ins using self-report tools.
Compensation
Not stated in the trial record.
Follow-up
The study measures changes from baseline at 4 weeks (Day 28-32).

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07298161

Evaluating SleepWhale Drops for Rest & Resilience

Recruiting
NAAll AgesInterventionalHealth services
Efforia, Inc
~100 participants
Updated 2025-12-23 on ClinicalTrials.gov
What's tested:SleepWhale Natural Sleep Drops

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
PROMIS Sleep Disturbance Scale
Measured over Change from baseline (Day 1-3) in PROMIS Sleep Disturbance Scale at 4 weeks (Day 28-32)
+3 more outcomes measured
Sleep
1 sites across 1 states
New York1

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Do you actually qualify for this trial?

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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 to supplement ingredients
Individuals on sleep Medication
Individuals with Gastrointestinal Issues
Individuals with Skin Conditions
Individuals Prone to Headaches
Individuals with Mental Health Conditions
Pregnant or Breastfeeding Individuals
Athletes and Competitive Participants
Individuals with Dependency Issues
Individuals with Dizziness or Fatigue Issues
  • PROMIS Sleep Disturbance ScaleChange from baseline (Day 1-3) in PROMIS Sleep Disturbance Scale at 4 weeks (Day 28-32)

    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 Short Form (e.g., 8a): 8-40 Score Interpretation Higher scores = worse sleep disturbance Lower scores indicate better sleep quality

  • Daytime Sleepiness Perception Scale (DSPS-4)Change from baseline (Day 1-3) in DSPS-4 at 4 weeks (Day 28-32)

    This survey is designed to measure your perception of daytime sleepiness. Please read each statement carefully and circle the response that best applies to your experience. Score Range Each item typically scored 0-4 or 1-5 Total score range (most common): 0-16 Score Interpretation Higher scores = greater perceived daytime sleepiness Lower scores indicate better daytime alertness

  • Fatigue Perception and Impact SurveyChange from baseline (Day 1-3) in FPIS at 4 weeks (Day 28-32)

    The Fatigue Perception and Impact Survey (FPIS) is a specialized questionnaire developed to evaluate the presence, severity, and impact of fatigue on an individual's life. Comprising a series of questions, the survey aims to capture both the subjective experience of fatigue and its consequences across various domains, such as physical, emotional, and social aspects. This tool is commonly used in clinical settings to assess fatigue in patients with various medical conditions, including chronic illnesses and cancer, helping healthcare professionals better understand and address the debilitating effects of fatigue on patients' quality of life. Researchers also employ the FPIS to gather valuable data on fatigue patterns. Score Range 0-4 or 1-5 Likert items Total score range 0-50 Score Interpretation Higher score= worse fatigue and greater functional impact Lower score= less perceived fatigue

  • Resilience Assessment ScaleChange from baseline (Day 1-3) in Resilience Assessment Scale at 4 weeks (Day 28-32)

    This survey aims to evaluate your level of resilience in different situations. Score Range 0-100 (scaled score) Score Interpretation Higher scores = greater resilience (better outcome) Lower scores indicate reduced psychological resilience