Skip to content
Study details
Enrolling now

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

Palo Alto Veterans Institute for Research
NCT IDNCT07069517ClinicalTrials.gov data as of Apr 2026
Target enrollment

160

Study length

about 3 years

Ages

18–65

Locations

1 site in TX

What this study is about

This trial is testing a treatment approach that combines cognitive behavioral therapy for insomnia and nightmares with sleep hygiene and written exposure therapy for PTSD. The treatment will be delivered in an accelerated group format over 1095 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Participate in Cognitive Behavioral Therapy for Nightmares (CBTn)
  • 2.Participate in Cognitive-Behavioral Therapy for Insomnia (CBTi)
  • 3.Participate in Sleep Hygiene
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Insomnia Severity Index (ISI)

Secondary: Depressive Symptoms Index-Suicidality Subscale (DSI-SS), Generalized Anxiety Disorder Screener (GAD-7), Patient Health Questionnaire-9 (PHQ-9)

Procedures

therapy