Development and preliminary evaluation of a telephone-based mindfulness training intervention for survivors of critical illness

Christopher E Cox, Laura S Porter, Pamela J Buck, Mary Hoffa, Derek Jones, Brenda Walton, Catherine L Hough, Jeffrey M Greeson, Christopher E Cox, Laura S Porter, Pamela J Buck, Mary Hoffa, Derek Jones, Brenda Walton, Catherine L Hough, Jeffrey M Greeson

Abstract

Rationale: Persistent symptoms of psychological distress represent an unmet need among intensive care unit (ICU) survivors.

Objectives: We aimed to develop and pilot test a simple telephone-based mindfulness training intervention to address this population's unique needs.

Methods: Open trial involving survivors of medical and surgical critical illness and their informal caregivers, using a pretest-posttest design.

Measurements and main results: We developed a six-session, telephone-delivered, ICU survivor-specific mindfulness intervention based on past focus groups, the medical literature, and the precedent of the most effective components of existing mindfulness programs. A total of 11 survivors of mechanical ventilation were enrolled, together with 2 informal caregivers for exploratory purposes. Three patients dropped out before intervention initiation because of progressive illness or severe social stressors. Of the 10 remaining participants, 8 (80%) completed the program within 7 weeks. Among these eight patients and caregivers who completed all study procedures, six (75%) experienced improvement in symptoms of psychological distress (anxiety, depression, or post-traumatic stress disorder). Changes in distress symptoms were correlated with improvement in mindfulness qualities, adaptive coping, and emotion regulation. Participants reported high satisfaction with the program in postintervention interviews.

Conclusions: A new ICU survivor-specific mindfulness training intervention delivered by telephone was acceptable and feasible. Changes in symptoms of distress were correlated with changes in skills that were targeted by the mindfulness program. Controlled trials are needed to further evaluate this promising intervention.

Figures

Figure 1.
Figure 1.
Study patient overview. The prospective evaluation of the mindfulness intervention used an uncontrolled, preintervention–postintervention design to assess the intervention’s feasibility, acceptability, and clinical impact, using validated measures of psychological distress. The two caregivers included are not shown. ICU = intensive care unit.
Figure 2.
Figure 2.
Depression, anxiety, and post-traumatic stress disorder symptoms over the course of the mindfulness intervention. Hospital Anxiety and Depression Scale (HADS) total, HADS anxiety domain, HADS depression domain, and Post-traumatic Symptom Scale (PTSS) questionnaire mean scores are shown pre- and postintervention for the eight participants who completed all study procedures. Caregiver scores are highlighted in red.

Source: PubMed

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