Sleep and Emotion Processing in Adolescent Post-traumatic Stress Disorder

Recruiting N/A Interventional Study
Post Traumatic Stress Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
14 – 18
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
180 (estimated)
Sponsor
University of Wisconsin, Madison · Other
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About This Trial
The goal of this clinical trial is to characterize the role of sleep, emotion processing, and daily affect in post-traumatic stress disorder (PTSD) and whether improving sleep quality using slow wave activity enhancement will impact next-day affect in youth. Participants will attend 4 study visits: * A clinical and trauma assessment visit * A testing day that may include cognitive testing, surve…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All participants must meet all of the following criteria: * Aged 14-18 years old, inclusive * Must agree to inform the investigators within 48 hours of any emergent medical conditions and procedures * Able to lie still on their back for up to 1 hour * Must not be pregnant * Mus…
Contacts

Sara Heyn, JD, PhD

303-296-2116

sheyn@wisc.edu

CONTACT