Effects of SleepWhale Drops on Sleep Quality and Daytime Well-being
This study aims to investigate how SleepWhale Drops affect your sleep quality and daytime well-being.
SleepWhale Natural Sleep Drops
Services Research Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.100 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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