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NCT05449990 · ClinicalTrials.gov registry record · NA

Family Presence on Multidisciplinary Patient Care Rounds in ICU

A NA study of Critical Illness, sponsored by Rutgers, The State University of New Jersey.

Completed
Registry status
NA
Development phase
390
Enrollment target
1
Study location

NCT05449990: Completed NA study of Critical Illness, sponsored by Rutgers, The State University of New Jersey.

NCT05449990 is a NA study of Critical Illness that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 390 participants, below the 3,134-participant average among 91 other Critical Illness trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05449990, a NA study of Critical Illness, has completed, sponsored by Rutgers, The State University of New Jersey.

COMPLETED
Registry status
NA
Development phase
390 participants
Enrollment target
1
Study location

Study Summary

Family presence on patient care rounds in adult intensive care units remains the least studied area of family-centered care. Despite support from professional organizations and critical care experts, very few critical care units in the United States have written policies allowing family presence (Davidson, 2013). This multidisciplinary prospective, quasi-experimental design study examined if there is a difference in patient and family satisfaction between rounding in the presence of family compared to patient rounding without family members in the adult intensive care unit and determined the nurses' and health care professionals' attitudes toward family presence during multidisciplinary patient care rounds in the ICU of two hospitals. The sample was 150 patients and family members (75 per hospital) and a convenience sampling of 90 healthcare professionals from the two sites. This investigation will have a potential impact on nursing practice and research. Findings obtained from this study may provide further concrete information on the effect of family presence during multidisciplinary patient care rounds, and patient and family satisfaction that will develop policies and standardized approaches to rounding processes that are innovative in diverse critical care settings as well as other non-critical care settings. Data obtained from this research will be used to create patient and family-centered care plans, add new knowledge and educational programs for healthcare professionals

Primary Outcome

Patient satisfaction with ICU stay was assessed using the Patient Satisfaction with Nursing Care Quality Questionnaire (PSNCQQ) scale. The instrument is a 19-item questionnaire. Cronbach's reliability estimates of 0.97. Participants' responses are provided using a 5-point Likert-type scale. Total possible scores range from 19-95. Lower total scores indicate greater satisfaction with nursing care. The scoring of the scale was: 1 = excellent, 2 = very good, 3 = good, 4 = fair, 5 = poor

Conditions Studied

Interventions

  • OTHER Participation in PFCC-IR

Study Locations (1)

New Jersey

  • Inspira Health Network - Mullica Hill

Trial Details

FieldValue
Enrollment Target 390 participants
Start Date 2021-07-26
Est. Completion 2022-07-30
Phase NA

What the finished NCT05449990 record still lists

NCT05449990 is an interventional study that assigns participants to a tested intervention. The registered 390 participants enrollment target is mid-sized for trials with a published cap, below the 3,134-participant average among 91 other Critical Illness trials with a reported enrollment target (88% lower).

The record links to 1 condition, with Critical Illness appearing as the primary indexed condition, and to 1 intervention - of which Participation in PFCC-IR is the first listed.

NCT05449990 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT05449990 about?

NCT05449990 is a clinical study titled "Family Presence on Multidisciplinary Patient Care Rounds in ICU". Family presence on patient care rounds in adult intensive care units remains the least studied area of family-centered care. Despite support from professional organizations and critical care experts, very few critical care units in the United States have written policies allowing family presence (Da...

What is the current status of trial NCT05449990?

This trial is currently completed. It is a NA study. The enrollment target is 390 participants. The study started on 2021-07-26. Estimated completion is 2022-07-30.

What conditions does trial NCT05449990 study?

This clinical trial studies the following conditions: Critical Illness.

What interventions are being tested in trial NCT05449990?

The interventions under investigation include: Participation in PFCC-IR (OTHER).

Who is sponsoring clinical trial NCT05449990?

This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05449990 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Critical Illness

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05449990's enrollment target sits among peer trials

390 35th of 91 higher than 57 of 91 other Critical Illness trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Critical Illness trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05449990, the US trial registry maintained by the National Library of Medicine. NCT05449990 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.