CompletedNot applicableNCT03391115
Official study title

Personalized Experiences to Inform Improved Communication for Minorities With Life Limiting Illness

Study summary

The purpose of this research is to develop patient-centered palliative care interventions to improve patient-provider communication and Quality of Life (QoL) of ethnic and racial minority patients living with life-limiting illnesses. Eliciting personal experiences is an effective way for patients to communicate their cultural values and beliefs. This study will assess how to integrate the patients' personal experience narratives into the electronic health record (EHR). The primary hypothesis is that the implementation of a patient-centered intervention to elicit personal experiences that are included in the EHR will improve patient-provider communication and patients' QoL.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedStorytelling Intervention for Patient Participants and Storytelling Intervention for Nurse Participants

The study team can explain what participation involves.

Who it may be forCOPD · Heart Failure

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Feb 18, 2021 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?University of Colorado, Denver

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
University of Colorado, Denver
Interventions being studied
Behavioral: Storytelling Intervention for Patient Participants; Behavioral: Storytelling Intervention for Nurse Participants
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Patients
  • 18 years of age or older
  • able to read English
  • capable of giving informed consent
  • self-identifying as part of a racial or ethnic minority
  • diagnosed with at least one LLI. The operational definition of LLI eligible for this study includes the following diagnoses: 1. metastatic solid cancer or inoperable lung cancer; 2. COPD with FEV1 values \< 35% predicted or oxygen dependence; 3. New York Heart Association Class III or IV heart failure (CHF). Inclusion criteria: Nurse
  • 18 years of age or older
  • Confirm verbally that they were involved in the care of a patient who is participating in the storytelling intervention

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • University of Colorado HospitalAurora, Colorado

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Feb 18, 2021. Always confirm current availability with the study team.

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