Improving Psychological Distress Among Critical Illness Survivors and Their Informal Caregivers

Improving Psychological Distress Among Critical Illness Survivors and Their Informal Caregivers

Project Period: 2012 - 2017 PI: Douglas White, MD, MAS
Funding Source: PCORI
Researchers: Christopher Cox, MD, Duke University (Co-PI)

Following release from the ICU, many patients and their caregivers report psychological distress including depression, anxiety, and PTSD, for over one year post-discharge. This distress poses a negative impact on their quality of life. Patients expressed that assistance with developing coping skills to deal with the physical and emotional changes of critical illness would be beneficial to them. In addition to these coping skills, patients reported that receiving more information about critical illness, recovery, and what to expect, would help alleviate some of their stress. 

Over 200 survivor-caregiver dyads were enrolled and randomized to receive one of two 6-week, telephone-based interventions - A) an ICU survivor-specific coping skills training (CST) program or B) a critical illness educational program. Researchers used surveys to compare the level of participant psychological distress and quality of life over the 6-month intervention period.

The study took place over three years at five different medical centers across the US. Researchers found that the CST program did not improve psychological distress symptoms when compared tot he education program. They did observe, however, that the CST program did improve symptoms of distress at 6 months among patients with high baseline distress, where the education program improved distress at 3 months among those ventilated for more than seven days. Researchers agreed that future efforts to address psychological distress among survivors should target high-risk populations. 

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