Family Procedural Presence



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:1/19/2019
Start Date:September 14, 2016
End Date:June 30, 2019
Contact:Valerie T Aston, MBA
Email:Valerie.Aston@imail.org
Phone:8015074606

Use our guide to learn which trials are right for you!

Stress and Engagement Surrounding ICU Procedures Among Patients, Families and Clinicians

This study seeks to determine the effect of a quality improvement policy regarding allowing
family members to remain in a patient's room during ICU procedures. The investigators
hypothesized that our change in policy to invite family members to remain during procedures
will improve patient & family engagement and improve long term psychological outcomes after
an ICU admission. The study also seeks to determine if inviting family members to remain in a
patient's room during ICU procedures will not increase clinician stress.

This is a research study about the effect of a quality improvement policy change regarding
family presence at ICU procedures on family and patient engagement, psychological outcomes
and stress levels in clinicians. In the study, ICU patients, their family members and ICU
clinicians will be surveyed regarding these outcomes, with some surveys obtained prior to a
policy change and a second set during a second time period after policy change. The patients
and family members will be asked survey questions after the procedure and 3 months later.
This study will also evaluate the change in clinician stress related to this policy change,
and clinicians will also answer survey questions.

Inclusion Criteria:

- 18 years old or older

- Able to read & speak English

- Family member of a patient or a patient that has undergone one of these procedures at
any point during the ICU stay (if the procedure occurs from Sunday at 8 am to Friday
at 12 pm): intubation, central line placement, arterial line placement, bronchoscopy,
thoracentesis, chest tube placement, paracentesis and lumbar puncture

- Physician (both attending physicians and trainees) and nurses who work in the ICU
during the study period.

Exclusion Criteria:

- Patients for whom no family member can be identified

- Non-English speaking individuals

- Children (<18 years of age)

- Participants with dementia, psychiatric disorder with psychosis, schizophrenia or
known cognitive dysfunction (established from chart review, report and/or score
greater than or equal to 3 on IQ Code screening).

- Provider who does not want to participate
We found this trial at
1
site
5121 S Cottonwood St
Murray, Utah 84157
(801) 507-7000
Principal Investigator: Sarah J Beesley, MD
Phone: 801-507-4606
Intermountain Medical Center Intermountain Medical Center is one of the most technologically advanced and patient-friendly...
?
mi
from
Murray, UT
Click here to add this to my saved trials