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Accelerated Treatment for Co-occurring Insomnia, Nightmares, and PTSD
NCT07069517 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- BEHAVIORAL Cognitive-Behavioral Therapy for Insomnia (CBTi)
- BEHAVIORAL Cognitive Behavioral Therapy for Nightmares (CBTn)
- BEHAVIORAL Written Exposure Therapy (WET)
- BEHAVIORAL Sleep Hygiene
Study Locations (1)
Texas
- Fort Hood — Kileen
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2025-12-02 |
| Est. Completion | 2028-12-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07069517
The ClinicalTrials.gov registry entry for NCT07069517 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Palo Alto Veterans Institute for Research, which has 50 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Insomnia appearing as the primary indexed condition, and to 4 interventions — of which Cognitive-Behavioral Therapy for Insomnia (CBTi) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07069517 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07069517 about?
NCT07069517 is a clinical study titled "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...
What is the current status of trial NCT07069517?
This trial is currently recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2025-12-02. Estimated completion is 2028-12-01.
What conditions does trial NCT07069517 study?
This clinical trial studies the following conditions: Insomnia, PTSD - Post Traumatic Stress Disorder, Nightmares. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07069517?
The interventions under investigation include: Cognitive-Behavioral Therapy for Insomnia (CBTi) (BEHAVIORAL), Cognitive Behavioral Therapy for Nightmares (CBTn) (BEHAVIORAL), Written Exposure Therapy (WET) (BEHAVIORAL), Sleep Hygiene (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07069517?
This trial is sponsored by Palo Alto Veterans Institute for Research, which has 50 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07069517 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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