SleepWhale Extra Strength Drops for deeper sleep and daytime resilience
Official title: Evaluating SleepWhale Drops for Rest & Resilience
Run by Efforia, Inc · NCT07298161 · Data updated 2026-11-12
This 30-day test will try whether nightly use of SleepWhale Natural Sleep Drops (a non-melatonin adaptogen and botanical formula) helps adults with sleep trouble sleep more deeply and feel better during the day.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Efforia, Inc Industry-sponsored |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | August 25, 2025 |
| Main results expected | August 25, 2026 |
| Study ends | August 25, 2026 |
| Registry record updated | December 23, 2025 |
| Trial ID | NCT07298161 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults in the United States who experience sleep disturbances, can read and understand English, are not using sleep medications, and are willing to follow the 30-day protocol and weekly check-ins are ideal candidates.
✕Probably not a fit
People who are on sleep medications, pregnant or breastfeeding, have certain medical conditions listed in the exclusions (including mental health, gastrointestinal, skin, headache, dizziness/fatigue issues), or who have severe clinical sleep disorders may not receive benefit from participating.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This decentralized, 30-day interventional study asks participants to take SleepWhale Natural Sleep Drops nightly and complete weekly check-ins using validated self-report sleep and daytime-function questionnaires. The product is an extra-strength, non‑melatonin blend of adaptogens and botanicals intended to support sleep depth and daytime resilience without causing grogginess or dependence. The trial emphasizes subjective experience over wearable-derived metrics, collecting self-reported outcomes on sleep quality, sleep disruptions, daytime performance, and overall resilience. Data will be used to determine whether regular nightly use of the drops corresponds with meaningful improvements in these patient-reported measures.
Why it matters
Potential benefit: If successful, the drops could offer a non‑melatonin, non‑habit forming option that helps people sleep better and feel more alert and resilient during the day.
How similar studies have gone: Some small trials of individual botanicals and adaptogens have shown mixed or modest effects on sleep, but high-quality, large-scale evidence for combined non‑melatonin formulations remains limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Can read and understand English. * US resident. * Willing and able to follow the requirements of the protocol. Exclusion Criteria: * 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
Where it's running
-
Efforia
New York, New York, United States Recruiting
Study contacts
- Study coordinator: Matthew Amsden
- Email: help@efforia.com
- Phone: 646-679-2479
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.