PTSD Clinical Trial
Official title:
Implementing an Intensive Care Unit (ICU) Diary Program at a Large Academic Medical Center: Results From a Randomized Control Trial Evaluating Psychological Morbidity Associated With Critical Illness
Verified date | April 2021 |
Source | Tulane University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Psychological morbidity in both patients and family members related to the intensive care unit (ICU) experience is an often overlooked, and potentially persistent, healthcare problem recognized by the Society of Critical Care Medicine as Post-intensive Care Syndrome (PICS). ICU diaries are an intervention increasingly under study with potential to mitigate ICU-related psychological morbidity, include ICU-related PTSD (post-traumatic stress disorder), depression and anxiety.
Status | Completed |
Enrollment | 60 |
Est. completion date | September 1, 2020 |
Est. primary completion date | September 25, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - admitted to the intensive care unit for at least 72 hours - sedated and mechanically ventilated for at least 24 hours. - available over-the-phone, up to 6 months post-ICU discharge Exclusion Criteria: - any patients who do not voluntarily agree to participate - not fluent in the English language - patients who have stayed in the ICU for less than 72 hours - patients who have been sedated and mechanically ventilated for less than 24 hours - patients with pre-existing severe psychotic illness, bipolar disorder, substance use disorder, PTSD, stroke, traumatic brain injury, neurocognitive impairment, or intellectual disability - patients with no phone number or reliable contact information for the sake of follow-up - prisoners - pregnant patients |
Country | Name | City | State |
---|---|---|---|
United States | Tulane University School of Medicine | New Orleans | Louisiana |
Lead Sponsor | Collaborator |
---|---|
Tulane University School of Medicine | The Arnold P. Gold Foundation |
United States,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in PTSD symptoms | Revised Impact of Event Scales (IES-R) score, measuring areas of hyperarousal, avoidance, and intrusion as subscales. Total score ranges from 0-88, higher score associated with worse PTSD symptoms. Scores from 1-22 are consistent with mild PTSD, and scores greater than 22 signal clinically significant PTSD symptoms. | at baseline (within one week of ICU admission) versus twelve-weeks post-ICU discharge | |
Secondary | Change in Hospital-associated Depression and Anxiety symptoms | Hospital Anxiety and Depression Scale (HADS), range of 0-21 for either anxiety or depression subscores, with higher scores corresponding to worse outcomes. Scores of 0-7 are normal, 8-10 are borderline abnormal (mild depression or anxiety), and 11-21 correspond to severe symptoms of anxiety or depression. | at baseline (within one week of ICU admission) versus twelve-weeks post-ICU discharge | |
Secondary | Change in Depression symptoms | Patient Health Questionnaire (PHQ-8), score ranges 0-24, as higher scores correspond to worse depression symptoms. Scores of 5-10 represent mild symptoms of depression, 10-15 signal moderate symptoms, and 15-24 correspond to severe symptoms. | at baseline (within one week of ICU admission) versus twelve-weeks post-ICU discharge | |
Secondary | Change in Anxiety symptoms | Generalized Anxiety Disorder 7-item scores (GAD-7) range from 0 to 21, with higher scores corresponding to worse anxiety symptoms. Scores of 0-4 indicate minimal anxiety, 5-9 correspond to mild anxiety, 10-14 signal moderate anxiety, and 15-21 represent severe anxiety. | at baseline (within one week of ICU admission) versus twelve-weeks post-ICU discharge |
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