Clinical Trials Directory

Trials / Unknown

UnknownNCT03808350

Family Procedural Presence

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Intermountain Health Care, Inc. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREFamilies Invited to Be Present at ProceduresFamily members will be invited (but not required) to remain in the ICU room during procedures, if patients agree
OTHERPlacebo/ControlFamily members will not be invited to remain in the ICU room

Timeline

Start date
2016-09-14
Primary completion
2019-03-31
Completion
2024-09-30
First posted
2019-01-17
Last updated
2022-04-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03808350. Inclusion in this directory is not an endorsement.