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NCT02641496 · ClinicalTrials.gov registry record · NA

Cognitive Behavioral Therapy to Increase CPAP Adherence in Veterans With PTSD

A NA study of Post Traumatic Stress Disorder and Obstructive Sleep Apnea, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
76
Enrollment target
1
Study location

NCT02641496: Completed NA study of Post Traumatic Stress Disorder and Obstructive Sleep Apnea, sponsored by VA Office of Research and Development.

NCT02641496 is a NA study of Post Traumatic Stress Disorder and Obstructive Sleep Apnea that has completed, run by VA Office of Research and Development. The registered enrollment target is 76 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02641496, a NA study of Post Traumatic Stress Disorder and Obstructive Sleep Apnea, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
76 participants
Enrollment target
1
Study location

Study Summary

Approximately 20 million Americans suffer from Obstructive Sleep Apnea (OSA) creating risks for major health problems, including dementia, heart attack, and stroke. Obesity, a growing problem for Americans and Veterans alike, is the greatest risk factor for the development of OSA. Male gender and smoking, other OSA risk factors, are common in Veterans. Given the high comorbidity of these risk factors in Veterans, OSA presents a significant health burden to Veterans. The investigators' prior work provides evidence that OSA occurs in up to 69% of Vietnam-era Veterans with Posttraumatic Stress Disorder (PTSD). OSA is easily treated; however, 15-30% of OSA patients are non-compliant with continuous positive airway pressure (CPAP), the standard OSA treatment. The proposed research aims to facilitate adherence to CPAP treatment by testing a novel cognitive-behavioral therapy intervention in Veterans with PTSD. If successful, it may represent an approach that could be applied to the rehabilitation of other chronic conditions with similar barriers to care.

Primary Outcome

The PAP machine will measure average PAP use in minutes at two timepoints: first 30 days (encompassing the first four weekly treatment sessions) and the last 30 days (final 30 days of the year long study).

Interventions

  • BEHAVIORAL Sleep Education
  • BEHAVIORAL CBT-OSA

Study Locations (1)

California

  • VA Palo Alto Health Care System, Palo Alto, CA - Palo Alto

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2017-01-01
Est. Completion 2023-12-31
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT02641496 record still lists

NCT02641496 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower).

The record links to 3 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Sleep Education is the first listed.

NCT02641496 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT02641496 about?

NCT02641496 is a clinical study titled "Cognitive Behavioral Therapy to Increase CPAP Adherence in Veterans With PTSD". Approximately 20 million Americans suffer from Obstructive Sleep Apnea (OSA) creating risks for major health problems, including dementia, heart attack, and stroke. Obesity, a growing problem for Americans and Veterans alike, is the greatest risk factor for the development of OSA. Male gender and sm...

What is the current status of trial NCT02641496?

This trial is currently completed. It is a NA study. The enrollment target is 76 participants. The study started on 2017-01-01. Estimated completion is 2023-12-31.

What conditions does trial NCT02641496 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Obstructive Sleep Apnea, PTSD.

What interventions are being tested in trial NCT02641496?

The interventions under investigation include: Sleep Education (BEHAVIORAL), CBT-OSA (BEHAVIORAL).

Who is sponsoring clinical trial NCT02641496?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02641496 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Post Traumatic Stress Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02641496's enrollment target sits among peer trials

76 143rd of 262 higher than 118 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02641496, the US trial registry maintained by the National Library of Medicine. NCT02641496 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.