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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05808179
Other study ID # 1R01HD102344
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2022
Est. completion date June 20, 2026

Study information

Verified date April 2023
Source VA Palo Alto Health Care System
Contact Jamie Zeitzer, PhD
Phone 6504935000
Email jzeitzer@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to determine whether a combination of a novel lighting intervention and a behavioral intervention are able to increase total sleep time in adolescents. The main questions this trial aims to answer are whether this combination therapy is able to meaningfully increase total sleep time in adolescents, and do so over a sustained period of time, and whether such a changes is associated with concomitant changes in mood and cognitive performance.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date June 20, 2026
Est. primary completion date June 20, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 14 Years to 18 Years
Eligibility Inclusion Criteria: 1. Aged 14-18 and a full-time student in grades 9-12 2. Male or female 3. Willing and with a schedule permitting them to go to bed at an earlier time 4. Planning on sleeping at home in their bedroom for at least 75% of the study Exclusion Criteria: 1. Currently taking any medications (including over-the-counter medications, e.g., melatonin) specifically for the treatment of sleep disorders 2. Sleep only in the prone (face-down) position

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Light
Broad-spectrum white light flashes are ~4000 lux, 2 msec long, occur every 20 s
Behavioral:
CBT
Cognitive behavioral therapy including psychoeducation, sleep hygiene, stimulus control, activity scheduling, motivational interviewing
Device:
Sham Light
Broad-spectrum white light flashes are ~4000 lux, 2 msec long, occur once

Locations

Country Name City State
United States Stanford University Stanford California

Sponsors (2)

Lead Sponsor Collaborator
Stanford University Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total sleep time Average nightly total sleep time 20 weeks
Secondary Melatonin timing Timing of the onset of salivary melatonin 8 weeks
Secondary Mood Score on the Center for Epidemiologic Studies Depression Scale for Children. Scored 0-60 with higher scores indicating greater depressive symptomatology. 20 weeks
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