Anxiety, Depression, Post Intensive Care Unit Syndrome, Psychological Trauma, PTSD
Conditions
Keywords
Post traumatic stress syndrome, Anxiety, Depression, PICS
Brief summary
The purpose of this study is to assess the use of an audio recording containing positive suggestion as a means to provide needed psychological support to critically ill patients in a feasible and reliable manner.
Detailed description
Following screening and consenting processes, patients will be randomized to enroll in interventional or control groups. The interventional group will listen to an audio recording of psychological support based on positive suggestion for about 30 min each day via headphones. At the time of ICU discharge, patients will be administered validated questionnaires to screen for symptoms of anxiety/depression (HADS), PTSD (IES-r), cognitive dysfunction (MOCA-blind), as well as evaluation of health status (EQ-5D). Six months post ICU discharge, patients will again be contacted and repeat the assessment with above questionnaires. Scores on the questionnaires will be compared between the groups at the two times points. Patient demographic data will also be obtained and assessed to contextualize study findings.
Interventions
OTHERPsychological Support Based on Positive Suggestion delivered via pre-recorded MP3 message
Daily administration of audiorecording
Sponsors
Mayo Clinic
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
Patients will be randomized 1:1 to intervention vs standard care. Using data from our prior observational study, mean (SD) HADS-Anxiety subscale was 7.3 (4.1) among these subjects (coefficient of variation = 4.1/7.3 = 0.56). A total 300 subjects will be enrolled and randomized until 100 subjects per arm recruitment target is reached to allow for mortality and dropout. The analysis will compare 6 month HADS-A by treatment arms using ANCOVA. The analysis will be conducted under a modified intention to treat principle, with subjects analyzed according to randomized arm, but excluding patients who die before follow up. Additional outcomes including HADS-D, MoCA-blind, and EQ-5D will be analyzed similarly using ANCOVA, and IES-R subscore\>1.6 will be analyzed by Chi-square test.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Acute respiratory failure and/or requiring vasopressors * Admitted to the ICU * Expected to stay \>48 hours in the ICU
Exclusion criteria
* History of dementia * History of mental retardation * History of suicide attempt * History of psychotic disorders such as schizophrenia * Acute alcohol/substance intoxication or withdrawal * Severe metabolic encephalopathy * Patients on comfort care * Patients not expected to survive the hospital stay * Those with hearing impairment * Non-English speaking.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Hospital Anxiety and Depression Scale (HADS) - Anxiety | within 96 hours of ICU discharge | A self-reported questionnaire designed to identify anxiety and depression. Each item is rated on a 4-point scale from 0 absence to 3 extreme presence. Total score is 21 per subscale: 0 - 7: Normal levels of anxiety/depression; 8-10: Borderline abnormal; \> 11: Abnormal. Total questions: 14 Anxiety 7 Depression 7 A self-reported questionnaire designed to identify anxiety and depression. Each item is rated on a 4-point scale from 0 absence to 3 extreme presence. Total score is 21. Per subscale: 0 - 7: Normal levels of anxiety/depression; 8-10: Borderline abnormal; \> 11: Abnormal. TL questions: 14: Anxiety 7, Depression 7 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Montreal Cognitive Assessment-Blind (MoCA-blind) | within 96 hours of ICU discharge | A screening tool designed to detect mild cognitive dysfunction. Subscores for each of the 5 sections are calculated. The total score is summed from the subscores, with a maximum score of 22. A score equal \> 18 is considered normal cognition. Total questions:13: Memory 3, Attention 4, Language 3, Abstraction 2, Orientation 1 |
| EQ-5D | within 96 hours of ICU discharge | A self-report questionnaire of health status or health-related quality of life. Scoring information: 5L - 5 levels of severity: no problems, slight problems, moderate problems, severe problems, extreme problems. The visual analog scale ranges from 0 to 100 with higher scores reflecting better perceived current health-related quality of life state. Total questions: 6 Mobility: 1 Self-Care: 1 Usual Activities: 1 Pain/discomfort: 1 Anxiety/depression: 1 Health State - Visual Analog Scale: 1 |
| Impact of Events Scale-Revised | within 96 hours of ICU discharge | A self-reported questionnaire designed to measure distress caused by traumatic events. Items are rated on a 5-point scale ranging from 0 (not at all) to 4 (extremely). Total scores are summed with higher scores indicating greater distress with regards to a specific event. Total questions: 22: Intrusion 7, Avoidance 8, Hyperarousal 7 |
| Hospital Anxiety and Depression Scale (HADS) - Depression | within 96 hours of ICU discharge | A self-reported questionnaire designed to identify anxiety and depression. Each item is rated on a 4-point scale from 0 absence to 3 extreme presence. Total score is 21. Per subscale: 0 - 7: Normal levels of anxiety/depression; 8-10: Borderline abnormal; \> 11: Abnormal. Total questions: 14: Anxiety 7, Depression 7 |
| Hospital Anxiety and Depression Scale (HADS) - Anxiety | 6 months following ICU discharge | A self-reported questionnaire designed to identify anxiety and depression. Each item is rated on a 4-point scale from 0 absence to 3 extreme presence. Total score is 21. Per subscale: 0 - 7: Normal levels of anxiety/depression; 8-10: Borderline abnormal; \> 11: Abnormal. Total questions: 14: Anxiety 7, Depression 7 |
Countries
United States
Outcome results
None listed