Recruiting

Effects of SleepWhale Drops on Sleep Quality and Daytime Well-being

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Study Aim

This study aims to investigate how SleepWhale Drops affect your sleep quality and daytime well-being.

What is being tested

SleepWhale Natural Sleep Drops

Dietary Supplement
Who is being recruted

See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: August 2025
See protocol details

Summary

Principal SponsorEfforia, Inc
Study ContactMatthew Amsden
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 25, 2025

Actual date on which the first participant was enrolled.

This study focuses on evaluating the effectiveness of SleepWhale Natural Sleep Drops (Extra Strength), a non-melatonin sleep aid made from adaptogens and botanicals. The goal is to improve sleep quality and daytime well-being, addressing common sleep issues like racing thoughts, restless nights, and sluggish mornings. The study aims to provide evidence on the benefits of SleepWhale, catering to the growing interest in natural remedies that offer support without the risk of grogginess or dependency. Participants will use SleepWhale Drops every night for 30 days, completing weekly check-ins using scientifically validated self-report tools. The study emphasizes the subjective experience of sleep quality and daytime functioning over metrics collected by sleep trackers or wearable devices. The primary objective is to assess the impact of regular SleepWhale use on self-reported sleep quality, sleep disruption incidents, daytime performance, and overall resilience. By participating, individuals contribute to their personal health and the broader research on SleepWhale's effectiveness.

Official TitleEvaluating SleepWhale Drops for Rest & Resilience
Principal SponsorEfforia, Inc
Study ContactMatthew Amsden
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

100 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

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

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Single arm where participants act as their own control

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Efforia

New York, United StatesOpen Efforia in Google Maps
Recruiting
One Study Center