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Completed

NCT Number: NCT03506438

Addressing Palliative Care Needs Among Intensive Care Unit Family Members

The quality of palliative care is highly variable for many patients treated in intensive care units (ICUs) and their family members. To address these challenges, the investigators will test the impact of a mobile app designed to help families navigate ICU-based palliative care vs. usual care. The investigators hypothesize that the intervention will reduce patient/family member unmet palliative care needs and improve the quality of clinical-family communication in racially/ethnically diverse populations.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Duke University

Durham, North Carolina, 27710, United States

About this study

The quality of palliative care is highly variable in an intensive care unit (ICU) setting. These markers of poor quality are even more common among Black patients and families than among Whites. To address these challenges, the investigators developed a mobile app that allows families to both give and receive information relevant to palliative care and for ICU clinicians to visualize patient/family data and therefore better support them.

To determine the effect of this intervention,the investigators propose to conduct a randomized clinical trial (RCT) comparing the intervention to usual care to address four specific aims: (1) Using a cluster randomized clinical trial, determine the effect of the intervention vs usual care on unmet needs, psychological distress symptoms, and patient-centered care; (2) Determine the impact of the intervention on unmet needs and patient-centered care based across different racial groups; and (3) Explore family member and clinician experiences with intervention using mixed methods to understand mechanisms within unique case contexts [exploratory aim]. The investigators hypothesize that compared to usual care, ICUconnect will reduce family members' unmet needs, reduce family member psychological distress, increase the patient-centeredness care, and reduce hospital length of stay overall--though the magnitude of effect will be greater among Blacks compared to Whites

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

PATIENTS

Inclusion criteria

  • ≥18 years of age
  • Receive mechanical ventilation in a study ICU for ≥48 hours under care of a study ICU physician

Exclusion criteria

(pre-consent):

  • Decisional capacity
  • Death expected within 24 hours
  • Admission to an ICU at the index hospital >14 days
  • Comfort care or withdrawal of treatment planned
  • Imprisoned
  • Extubated and possess decisional capacity prior to informed consent
  • Died before T2 survey complete
  • No known family or surrogate
  • Care assumed by a non-study ICU attending after consent by patient/family but before T1
  • Care assumed by non-study ICU attending <3 days after T1 but before T2
  • Study ICU attending physicians from different groups (i.e., intervention or control) caring for patient change <3 days after T1 completed by family

Exclusion criteria

(post-consent):

  • Patient regains decision making capacity before T2
  • Patient dies before T2

FAMILY MEMBER

Inclusion criteria

  • ≥18 years of age
  • Self-described as the individual (related or unrelated) who provides the most support and with whom the patient has a significant relationship (per definition of 'family' described in the Society of Critical Care Medicine 2016 Guidelines for Family-Centered Care in the Neonatal, Pediatric, and Adult ICU)

Exclusion criteria

(pre-consent):

  • Lack a knowledge of English such that the potential participant is not confident that they could complete study tasks (app viewing, surveys)
  • Imprisoned
  • Unable to complete surveys for any reason
  • Describe their race as neither White nor Black*
  • Describe their ethnicity as Hispanic*
  • Note that this study explicitly targets issues of racial disparities in healthcare, particularly of Black / African-Americans. Hispanics are excluded because of the pervasive nature of US residents' general belief that 'Hispanic' is a racial category.

Exclusion criteria

(post-consent):

  • If the assigned randomized ICU attending physician either leaves ICU service or is replaced by a non-participating ICU physician <= 2 calendar days after family member completes T1 survey
  • Low need burden (NEST score <15)*

ICU PHYSICIANS

Inclusion criteria

  • ≥18 years of age
  • Attending physician in a study ICU

Exclusion criteria

  • None

*The NEST score cutoff was changed on June 26, 2019. At this point, 3 patients had been randomized. This change was based on our review of data (NEST + psychological distress symptoms) from a parallel cohort study of >50 family members of ICU patients who met nearly identical eligibility criteria as for the ICUconnect trial. This was a larger cohort than the pilot study on which we based the NEST cutoff.

Treatment and study plan

Needs-focused mobile app

Behavioral

A mobile web app designed to assist both ICU clinicians in addressing patient/family needs and families in reporting their unmet needs.

Usual Care

Other

Usual ICU care as per the standards of the ICU attending

Primary outcomes

  1. Needs; Existential Concerns; Symptoms; and Therapeutic Interaction (NEST) Scale Total Score

    Time frame: Time 1 (baseline), Time 2 (target ~3 days post-randomization), and Time 3 (target ~1 week post-randomization)

    A palliative care needs instrument that assesses palliative care needs across all 8 domains of palliative care quality. Scores on this 13-item instrument can range from 0 (no needs) to 130 (higher needs)

Secondary outcomes

  1. Patient Health Questionnaire 9-Item Scale (PHQ-9)

    Time frame: Time 1 (baseline), Time 2 (target ~3 days post-randomization), and Time 4 (3 months post-randomization)

    A depression symptoms instrument. Scores range from 0 (no depression symptoms) to 27 (higher depression symptoms)

  2. Generalized Anxiety Disorder 7-Item Scale (GAD-7)

    Time frame: Time 1 (baseline), Time 2 (target ~3 days post-randomization), and Time 4 (3 months post-randomization)

    An anxiety symptoms instrument. Scores range from 0 (no anxiety symptoms) to 21 (higher anxiety symptoms)

  3. Post-Traumatic Stress Symptom (PTSS) Inventory

    Time frame: Time 1 (baseline) and Time 4 (3 months post-randomization)

    A post-traumatic stress disorder symptom instrument. Scores range from 10 (low PTSD symptoms) to 70 (higher PTSD symptoms)

  4. Number of Participants With Goal Concordant Care

    Time frame: Time 1 (baseline) and Time 2 (target ~3 days post-randomization)

    A measure of the alignment between patient values and treatments received. This is a dichotomous scale; care is either concordant or discordant.

  5. Post-randomization Hospital Length of Stay (Days)

    Time frame: Across the entire hospitalization after randomization (approximately 2 months)

    Patient hospital length of stay measured in days post-randomization

  6. Post-randomization Intensive Care Unit Length of Stay (Days)

    Time frame: Across the entire hospitalization after randomization (approximately 2 months)

    Patient intensive care unit length of stay post-randomization

  7. Number of Participants Who Responded "Usually" or "Always" on the Interpersonal Processes of Care 18-Item (IPC-18) Short Form Scale - Communication Domain

    Time frame: Baseline (at time of randomization) and ~3 days post-randomization

    The IPC-18 is a measure of the interpersonal aspects of care. Interpersonal processes of care are the social-psychological aspects of the patient-physician interaction. These components of quality of care may help explain disparities in health between minority patients and their counterparts. The "elicited concerns, responded" scale within the Communication domain is used here. All items use an identical set of response options: 1='never'; 2='rarely'; 3='sometimes'; 4='usually'; 5='always.' A higher score indicates better processes.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

Registry information

Acronym: ICUconnect

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Apr 24, 2018
Registry last updated
Nov 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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