Actively Recruiting

Phase Not Applicable
Age: 18Years - 21Years
All Genders
NCT06768749

The Impact of Melatonin Lotion on Sleep and Mental Health

Led by University of Redlands · Updated on 2026-05-01

60

Participants Needed

1

Research Sites

161 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to examine the effect that melatonin lotion has on sleep quality, the nervous system, and mental health. Melatonin is a hormone secreted by the brain that regulates sleep and might improve depression and anxiety symptoms. The goal is to determine whether melatonin in lotion form is an effective treatment for young adults with inadequate sleep and might improve mental health. Participants will fill out surveys, wear an actigraph (a wrist-worn device that measures sleep), wear a heart rate monitor (a strap worn around one's chest), and provide nightly saliva samples during treatment weeks. In one of the two treatment weeks, participants will receive a lotion that contains melatonin. During the other week they will receive a control treatment that will be lotion with no melatonin, and there will be a week in between with no treatment at all.

CONDITIONS

Official Title

The Impact of Melatonin Lotion on Sleep and Mental Health

Who Can Participate

Age: 18Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a T score of 48 or higher on the PROMIS sleep disturbance short form
  • Have a T score of 55 or higher on the PROMIS anxiety or depression short form (mild symptoms or more)
  • Are between 18 and 21 years old
  • Are willing to keep a consistent bedtime (within ±1 hour) during treatment weeks
  • Are able to apply lotion and complete study procedures
Not Eligible

You will not qualify if you...

  • Currently using antidepressant, anti-anxiety, or sleep medications including melatonin
  • Are pregnant
  • Have allergies or sensitivities to scented lotion
  • Are unwilling to keep a consistent bedtime (within ±1 hour) during treatment weeks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Redlands

Redlands, California, United States, 92374

Actively Recruiting

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Research Team

L

Lisa E Olson, Ph.D.

CONTACT

S

Steven Moore, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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