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Family Procedural Presence

Intermountain Health Care, Inc. logo

Intermountain Health Care, Inc.

Status

Active, not recruiting

Conditions

Patient and Family Engagement

Treatments

Procedure: Families Invited to Be Present at Procedures
Other: Placebo/Control

Study type

Interventional

Funder types

Other

Identifiers

NCT03808350
1050086

Details and patient eligibility

About

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.

Full 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.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

120 participants in 2 patient groups, including a placebo group

Families Excluded From Presence at Procedures
Placebo Comparator group
Description:
Families not invited to remain for ICU procedures
Treatment:
Other: Placebo/Control
Families Invited to Be Present at Procedures
Active Comparator group
Description:
Families invited to remain for ICU procedures
Treatment:
Procedure: Families Invited to Be Present at Procedures

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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