The impact of prolonged exposure on sleep and enhancing treatment outcomes with evidence-based sleep interventions: A pilot study

Elizabeth M Walters, Melissa M Jenkins, Carla M Nappi, Jacob Clark, July Lies, Sonya B Norman, Sean P A Drummond, Elizabeth M Walters, Melissa M Jenkins, Carla M Nappi, Jacob Clark, July Lies, Sonya B Norman, Sean P A Drummond

Abstract

Objective: Insomnia and nightmares are central features of posttraumatic stress disorder (PTSD). However, often they are inadequately assessed and ineffectively resolved following gold-standard PTSD treatment. Here we: (a) evaluate effects of prolonged exposure (PE) on subjectively measured sleep and (b) present pilot results of an examination of whether adding sleep interventions (imagery rehearsal therapy [IRT] and cognitive-behavioral therapy for insomnia [CBT-I]) to PE improves treatment response, relative to PE alone, for night- and/or daytime PTSD symptoms among returning U.S. veterans and postdeployment personnel.

Method: In a parallel-groups, randomized controlled trial, participants received 12 sessions of PE followed by IRT (5 weeks) and CBT-I (7 weeks) or PE followed by 12 weeks supportive care therapy (SCT).

Results: PE did not improve sleep to a clinically meaningful degree, despite significant improvements in both Clinical Administered PTSD Scale and PTSD Checklist. Enhancing treatment with IRT/CBT-I led to greater improvements in insomnia (diary-recorded sleep efficiency) symptoms with large effect size, relative to SCT (p = .068, d = 1.07). There were large improvements in nightmare frequency relative SCT that did not reach statistical significance (p = .11, d = 0.90). Moreover, there was small improvement in daytime symptoms (Clinical Administered PTSD Scale) that did not reach statistical significance (p = .54, d = .31).

Conclusion: The addition of targeted, validated sleep treatment improves effects of PE and improves nighttime symptoms. Thus, evidence-based sleep treatment should be considered in comprehensive PTSD treatment. (PsycINFO Database Record (c) 2020 APA, all rights reserved).

Trial registration: ClinicalTrials.gov NCT01009112.

Conflict of interest statement

Conflicts of Interest

The authors declare no conflicts of interest associated with this publication.

Figures

Figure 1.
Figure 1.
Consort chart.
Figure 2.
Figure 2.
M ± SD scores at week 0 (baseline) and 6 (post-PE). Arrows indicate direction of improvement. Dotted lines indicate clinical thresholds used: for CAPS, Moderately severe (60) and Probably PTSD (40); Sleep Efficiency 85%; Number of Nightmares 2/week. *p < .05, ***p<.001.
Figure 3.
Figure 3.
M ± SD scores at each assessment – week 0 (pre-treatment), 6 (post-PE), 11 (post-IRT or 5 weeks SCT) and 18 (post-IRT/CBTI or 12 weeks SCT) for the Evidence-Based Sleep Treatment (blue/light grey) and SCT (red/dark grey) groups. For SCT, n = 11 (weeks 0 and 6) and n = 8 (weeks 11 and 18). For Evidence-Based Sleep Treatments, n = 12 (weeks 0 and 6), n = 6 (week 11) and n = 7 (week 18). Arrows indicate direction of improvement. Dotted lines indicate clinical thresholds used: for CAPS, Moderately severe (60) and Probably PTSD (40); Sleep Efficiency, 85%; Number of Nightmares, 2/week. * p < .05.

Source: PubMed

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