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Treatment of Nightmares in Psychiatric Inpatients With Imagery Rehearsal Therapy: An Open Trial and Case Series.

Thomas E Ellis, Katrina A Rufino, Michael R Nadorff

Behavioral Sleep Medicine January 1, 2019 DOI: 10.1080/15402002.2017.1299738 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

Imagery Rehearsal Therapy (IRT) reduced nightmare frequency and intensity and improved sleep and other symptoms, including suicidal ideation, in 20 adult psychiatric inpatients with multiple treatment-resistant conditions. No adverse reactions occurred. Because the study was an open trial without a control group, it cannot conclude that IRT specifically caused these improvements; larger controlled trials are needed.

Study at a glance

Characteristics Case series Case report Peer reviewed
Sample size 20
Population Adult psychiatric inpatients with multiple treatment-resistant comorbid conditions (mood, anxiety, personality, and substance-related disorders), excluding active psychosis or significant cognitive impairment
Intervention Imagery Rehearsal Therapy
Duration 3 weeks with 4 small group sessions
Key finding Imagery Rehearsal Therapy was associated with significant reductions in nightmare frequency and intensity and improvements in sleep and other symptoms in psychiatric inpatients.

Abstract

Objectives: This study sought to assess the utility of Imagery Rehearsal Therapy (IRT) for nightmares in an inpatient psychiatric setting. Although IRT enjoys a substantial evidence base for efficacy in various populations, data with psychiatric inpatients are lacking. Participants: Participants were 20 adult psychiatric inpatients (11 male, 9 female; mean age=43.4), in an extended stay psychiatric inpatient facility. All participants were diagnosed with multiple, treatment resistant, comorbid conditions, including mood disorders, anxiety disorders, personality disorders, and substance-related disorders. Patients with active psychosis or significant cognitive impairment were excluded. Methods: This was an open trial utilizing a case series design. In addition to routine hospital treatment that included psychotherapeutic and pharmacological interventions, participants received IRT over a span of 3 weeks in 4 small group sessions. Included were education about sleep and nightmares, instruction in writing new dream narratives and practicing guided imagery, and support via further consultation and trouble-shooting. Patients were referred by their psychiatrist or were self-referred, with approval from their treatment teams. Results: Results showed significant aggregate reductions in nightmare frequency and intensity, as well as improvement in sleep overall. Patients also improved on a variety of other symptom measures, including suicidal ideation. No adverse reactions were observed. The present report includes a sampling of individual case vignettes to illustrate variability in treatment response. Conclusions: This study provides preliminary evidence that IRT can be used safely and effectively in a hospital environment to benefit patients suffering from serious mental illnesses, often in the midst of significant life crises. It is not possible in this preliminary study to conclude that IRT specifically (as opposed to other aspects of hospital treatment) produced these outcomes. Larger, controlled trials are needed to establish a causal connection between IRT and nightmare reduction.

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