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Behavioural Intervention
Psychological Support for Critical Illness
N/A
Recruiting
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Critically ill adult patients (age >18) requiring non-invasive ventilation, high flow O2 or mechanical ventilation and expected to stay >48 hours.
Be older than 18 years old
Must not have
patients on comfort care
psychotic disorders such as schizophrenia
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 96 hours after icu discharge and 3 months after hospital discharge
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether a daily psychotherapeutic approach can help critically ill patients.
Who is the study for?
This trial is for critically ill adults over 18 who need breathing support like non-invasive ventilation or mechanical ventilation and will likely stay in the ICU for more than 48 hours. It's not for those with dementia, severe brain dysfunction due to liver problems, on end-of-life care, unlikely to survive their hospital stay, don't speak English, have a history of serious mental illness or substance issues.
What is being tested?
The study tests a psychological support method using positive suggestions given daily in the ICU. The goal is to see if this approach helps improve mental health and cognitive function in patients facing critical illnesses.
What are the potential side effects?
Since this intervention involves psychological support rather than medication, traditional side effects are not expected. However, there may be emotional responses or discomfort related to discussing one’s condition and receiving reassurance.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am an adult in critical condition needing breathing support and expected to stay in care for more than 48 hours.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am receiving care focused on my comfort.
Select...
I have been diagnosed with a psychotic disorder like schizophrenia.
Select...
I have a severe brain disorder due to a metabolic problem.
Select...
I do not speak English.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 96 hours after icu discharge and 3 months after hospital discharge
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 96 hours after icu discharge and 3 months after hospital discharge
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
minimal important change in hospital anxiety and depression scale - Anxiety
Secondary study objectives
minimal important change in hospital anxiety and depression scale-Depression
Other study objectives
EQ-5D-3L
minimal important change in Impact of Event Scale-Revised
statistically significant improvement in MoCA-blind
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: DoulaExperimental Treatment1 Intervention
Group II: No InterventionActive Control1 Intervention
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,333 Previous Clinical Trials
3,059,990 Total Patients Enrolled
17 Trials studying Critical Illness
42,517 Patients Enrolled for Critical Illness
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am receiving care focused on my comfort.I have been diagnosed with a psychotic disorder like schizophrenia.You have an intellectual disability.You have a history of memory loss or forgetfulness.You are currently experiencing the effects of drugs or alcohol, or are going through withdrawal.You have attempted to harm yourself in the past.I am an adult in critical condition needing breathing support and expected to stay in care for more than 48 hours.I have a severe brain disorder due to a metabolic problem.I do not speak English.
Research Study Groups:
This trial has the following groups:- Group 1: No Intervention
- Group 2: Doula
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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