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Effects of CPAP Therapy on PTSD Symptoms

Completed
Conditions
Obstructive Sleep Apnea
Quality of Life
Sleep
PTSD
Registration Number
NCT02019914
Lead Sponsor
Veterans Medical Research Foundation
Brief Summary

The purpose of this study is to evaluate the effects of treating Obstructive Sleep Apnea (OSA) with continuous positive airway pressure (CPAP) therapy on symptoms of post traumatic stress disorder (PTSD). The study hypotheses are that CPAP use will improve PTSD symptoms overall and that CPAP use will improve sleep quality and duration, nocturnal symptoms related to PTSD, mood, daytime sleepiness, sleep-related quality of life, and general health perception.

Detailed Description

Post traumatic stress disorder (PTSD) is associated with increased healthcare utilization, decreased functional status, and overall poor health. Sleep disturbances in PTSD are common, including nightmares, dream enactment, and poor sleep quality. Obstructive sleep apnea (OSA) is also highly prevalent in the veteran population and may exacerbate PTSD symptoms by triggering arousals from sleep that promote recollection of dreams, enactment of dreams, and disrupt sleep continuity. Improvements in sleep quality and PTSD symptoms have been reported when OSA is treated with continuous positive airway pressure (CPAP) therapy. However, formal assessment using validated questionnaires and documentation of CPAP compliance to correlate with these tools has not yet been performed. This study will recruit veterans with PTSD who have been newly diagnosed with OSA and who are willing to try CPAP therapy. Baseline assessments of PTSD symptoms, daytime sleepiness, sleep-related quality of life, sleep quality, general health perception, and mood will be performed before initiation of treatment and after 3 and 6 months of therapy.

This study will have the following specific aims:

Aim 1: To evaluate the effect of CPAP use on PTSD symptoms.

Hypothesis: After 6 months of treatment, CPAP use will improve PTSD symptoms as assessed by the PTSD checklist (PCL-S).

Aim 2: To evaluate the effect of CPAP use on 1)sleep quality and duration, 2)nocturnal symptoms of nightmares, movement disorders, dream enactment, and insomnia, 3)mood, 4)daytime sleepiness, 5)sleep-related quality of life, and 6) general health perception.

Hypothesis: After 6 months of treatment, CPAP use will improve sleep quality, sleep duration, mood, daytime sleepiness, sleep-related quality of life, general health perception, and nocturnal symptoms of nightmares, movement disorders, dream enactment, and insomnia.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
59
Inclusion Criteria

The intent is to recruit a study population that is as representative as possible of the veteran PTSD population. Thus, entry criteria are as inclusive as possible:

  • age >18 year
  • confirmed diagnosis of PTSD (PCL checklist minimum score of 45)
  • confirmed diagnosis of sleep apnea (apnea hypopnea index >5/h)
  • newly starting CPAP (not previously treated)
Exclusion Criteria
  • fatal co-morbidity with life expectancy of less than 6 months,
  • residing in a geographically remote area that would make follow up at 3 and 6 months difficult.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in PTSD symptoms measured by the PTSD checklist (PCL-S).Baseline, 3 months, 6 months

A change of -10 points on the PCL-S has been previously determined to be clinically significant.

Secondary Outcome Measures
NameTimeMethod
Daytime Sleepiness measured by the Epworth Sleepiness Scale (ESS)Baseline, 3 months, 6 months
Sleep Related Quality of life with be assessed using the Functional Outcomes of Sleep Questionnaire (FOSQ-10).Baseline, 3 months, 6 months

The FOSQ-10 consists of 10 questions, with a lower score indicating more difficulty with activity due to poor sleep.

Depression will be assessed using the Patient Health Questionnaire-9 (PHQ-9).Baseline, 3 months, 6 months

The PHQ-9 is a self report depression measure and is a quick, valid assessment of depression. Depression is a common comorbid condition with PTSD.

General health related quality of life.Baseline, 3 months, 6 months

This will be assessed using a likert scale question asking subjects to rate their quality of life for 2 preceding days based on spiritual, emotional, physical, social and financial aspects of their lives.

Change in sleep quality assessed by the Pittsburgh Sleep Quality Index (PSQI).Baseline, 3 months, 6 months

This is a 19 item self-report assessment of sleep quality and degree of sleep difficulties over the past month. A global score\>/=5 is considered poor sleep quality.

Trial Locations

Locations (1)

VA San Diego Healthcare System

🇺🇸

San Diego, California, United States

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