Evaluating SleepWhale Drops for Rest & Resilience

Efforia, Inc

Status: Enrolling

Conditions: Sleep

Treatments: Dietary Supplement: SleepWhale Natural Sleep Drops

Study type: Interventional

Funder types: Industry

Identifiers

NCT07298161

37640

Details and patient eligibility

About

30-day study evaluating SleepWhale Natural Sleep Drops (Extra Strength)-formulated to support deeper sleep and better days.

Full description

This remotely administered decentralized trial is designed to rigorously evaluate the efficacy of SleepWhale Natural Sleep Drops (Extra Strength), a non-melatonin sleep aid composed of adaptogens and botanicals, in improving sleep quality and daytime well-being. Recognizing the pervasive issues of sleep disturbances including racing thoughts, restless nights, and sluggish mornings, and the growing interest in natural remedies that provide support without the risk of grogginess or dependency, this study aims to provide empirical evidence on the benefits of SleepWhale.

Participants in this trial will incorporate SleepWhale Drops into their nightly routine for a duration of 30 days. Throughout this period, participants are required to complete weekly check-ins utilizing scientifically validated self-report tools. This approach is chosen to emphasize the subjective experience of sleep quality and daytime functioning over metrics that might be collected by sleep trackers or wearable devices, which, while useful, can sometimes lack accuracy and fail to capture the entirety of an individual's sleep experience.

The primary objective of this study is to assess the impact of regular nightly use of SleepWhale Natural Sleep Drops on several key outcomes, including self-reported sleep quality, incidences of sleep disruption, daytime performance, and overall resilience. By focusing on these areas, the study aims to gather meaningful data that reflects the real-world effectiveness of SleepWhale Drops in supporting restful sleep and enhancing daytime productivity and well-being.

Ultimately, by participating in this trial, individuals will not only contribute to their personal health and well-being but also to the larger body of research aimed at validating the effectiveness of SleepWhale Natural Sleep Drops. This study stands as a critical step towards separating trend from truth, offering participants and the wider community real outcomes and insights into the potential of SleepWhale as a natural solution for better sleep and brighter days.

Enrollment: 100 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

Single arm where participants act as their own control

Experimental group

Description:

Single arm where participants act as their own control

Treatment:

Dietary Supplement: SleepWhale Natural Sleep Drops