Nightmares

2

Review clinical trials related to Nightmares. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Accelerated Treatment for Co-occurring Insomnia, Nightmares, and PTSD

This study is a two-arm individually randomized group treatment clinical trial evaluating behavioral therapies for insomnia, nightmares, and PTSD. The study will compare cognitive-behavioral therapy for insomnia and nightmares to sleep hygiene (Control), both integrated with Written Exposure Therapy for PTSD and delivered in an accelerated (i.e., 5-day) group treatment format, preceded and followed by individual treatment sessions. 160 participants will be randomized into one of two study conditions.

Participants needed: 160
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Palo Alto Veterans Institute for ResearchUpdated: Dec 3, 2025Locations: 1
Eligibility criteria

Defense Enrollment Eligibility Reporting System (DEERS) eligible active-duty mil... [+5]

Current suicide or homicide risk meriting crisis intervention. [+6]

Status: Recruiting

Restorative Early Sleep Treatment After the Emergency Department

The goal of this randomized controlled trial is to pilot the virtual delivery of cognitive behavioral therapy for insomnia (CBT-I) and nightmares (CBT-I\&N) via telehealth as an early intervention for treating posttraumatic sleep disturbance in acute trauma patients exposed to interpersonal violence. The main aims are to: 1. Test the acceptability, feasibility, and satisfaction of sleep-focused CBT delivered early after trauma 2. Evaluate the impact of sleep-focused CBT delivered early after trauma on sleep disturbance 3. Evaluate the impact of sleep-focused CBT delivered early after trauma on PTSD symptoms The investigators will compare CBT-I and CBT-I\&N to sleep education control. Participants will meet with a provider for 6 weekly sessions via telehealth and complete surveys on the participants' symptoms.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Henry Ford Health SystemUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Michigan residents treated at Henry Ford Hospital [+8]

Presenting to ED for non-interpersonal trauma [+21]