- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03874676
Exploration of Patient Ethics and Communication Excellence (PEACE) Rounds
Exploration of Patient Ethics and Communication Excellence (PEACE) Rounds for Patient Care Providers: A Thematic Analysis
Study Overview
Detailed Description
Qualitative data about participants' experiences throughout the PEACE Rounds will be collected using semi-structured interviews and participant observation. This data will be analyzed to describe and explain the perceptions that emerge from participant experience.
Qualitative Sampling Purposive samples are identified to initiate data collection and analysis, and then are used to select participants who are likely to clarify, verify, or contradict data as it is collected. Sampling concludes when the data are "saturated," which means the coded categories are well-defined and no new significant insights are emerging from additional interviews.
Semi-structured Interviews
The study team will conduct semi-structured interviews, which will be recorded and transcribed, following a consented subject's participation in at least one PEACE round. Open-ended questions, intended to elicit participants' perspectives on their experience of PEACE Rounds, will frame the interview. These are:
"What/who do you remember most vividly?" "What was most meaningful to you? "What would you change about the experience, if you could? " "Would you do it again? Why or why not?" "What, if anything, changed after PEACE rounds?"
Observation PEACE Rounds will be observed by the PI to collect data that will provide further insight to participants' experiences. Observations of interactions and reactions in real time will be documented and the data will be coded and analyzed using thematic analysis methods. Observational data will not be integrated into interview data but will be used to confirm or contrast reported data.
Qualitative Data Analysis Qualitative methodology does not seek to verify hypotheses based on logical assumptions, as quantitative measures do, instead it is used to derive salient constructs directly from the data. This methodology allows inductive understanding of participants' perceptions of their participation in PEACE Rounds.
The qualitative data will be analyzed according to the thematic analysis method based on that of Braun and Clarke . the researcher has become familiar with the data and generated an initial list of ideas that are relevant to the research objective, codes will be generated. The codes will reflect a specific feature of the data that further explicates it. After the data has been coded, the researcher will look for how different codes can be combined to create overarching themes. When there is essentially no new information coming from the codes, the data is considered saturated and no new themes are created. At this point, the researcher will review the themes and refine them, so they can be expressed in a data map expressing how they fit together to tell the story of the data.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Florida
-
Orlando, Florida, United States, 32804
- AdventHealth Orlando
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- An employee of AdventHealth (AH), or a physician with privileges there, who has participated in PEACE Rounds at AdventHealth.
- Over the age of 18
- Able to provide informed consent
- Must speak and understand English
Exclusion Criteria:
1. Discernable cognitive impairment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
PEACE Rounds Clinicians
Nurses, physicians, care managers, chaplains, and other clinicians who attend PEACE rounds as part of their routine work in the hospital.
|
PEACE Rounds are a routine process for providing self help to clinicians who care for difficult patients from the perspective of ethics and the need for cross-disciplinary communication.
PEACE Rounds participants will be interviewed about how they experience the rounds and for their perspective on the effects on their own wellness and resilience.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Thematic Analysis of Interview Data to Describe Effects of PEACE Rounds on Burnout Relief
Time Frame: 6 months
|
Analysis of data collected throughout the study, using saturation sampling and documented coding techniques, will result in thematic descriptions of the aggregated experiences of clinical staff who participate in PEACE rounds.
Semi-structured interviews will measure the extent to which PEACE Rounds are an effective component on self-help for clinicians and other healthcare workers who care for patients with difficult or controversial treatment plans.
Interview questions will include: "What/who do you remember most vividly?" "What was most meaningful to you?" "What would you change about the experience, if you could?" "Would you do it again?
Why or why not?" "What, if anything, changed after PEACE rounds?"
|
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kim S. McManus, Ph.D., AdventHealth Center for CREATION Research
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1398203
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Resilience
-
Emory UniversityCompletedBehavioral Resilience | Biological ResilienceUnited States
-
The Center for Mind-Body MedicineSimon Family FoundationEnrolling by invitation
-
Icahn School of Medicine at Mount SinaiCompleted
-
The Center for Mind-Body MedicineHerbert Simon Family FoundationEnrolling by invitation
-
Chinese University of Hong KongAlice Ho Miu Ling Nethersole HospitalCompleted
-
Göteborg UniversityIOGT-NTO's Junior AssociationUnknownResilience
-
City University of Hong KongInternational Social Service Hong Kong BranchCompleted
-
Leibniz-Institut für Resilienzforschung (LIR) gGmbHEuropean Regional Development Fund; Ministry of Science and Health of Rhineland-Palatinate... and other collaboratorsRecruiting
-
Leibniz-Institut für Resilienzforschung (LIR) gGmbHEuropean Regional Development Fund; Ministry of Science and Health of Rhineland-Palatinate... and other collaboratorsRecruiting
-
Duke UniversityCompleted
Clinical Trials on PEACE Rounds
-
University of PennsylvaniaMichigan State University; Institute of Education SciencesEnrolling by invitation
-
Icahn School of Medicine at Mount SinaiCompleted
-
Bar-Ilan University, IsraelCompleted
-
University of PittsburghNational Institute on Minority Health and Health Disparities (NIMHD); National...RecruitingViolence, Domestic | Coping Skills | Adolescent Behavior | Violence, Sexual | Violence, Non-accidental | Group, Peer | Emotional Abuse | Communication, PersonalUnited States
-
The University of Texas Health Science Center,...Agency for Healthcare Research and Quality (AHRQ)CompletedBreast CancerUnited States
-
The University of Texas Health Science Center,...CompletedPostpartum | Physician RoundsUnited States
-
Icahn School of Medicine at Mount SinaiTerminatedPatient Satisfaction | Healthcare Practitioner StressUnited States
-
University of California, DavisRecruitingPediatric Disorder | Neonatal DiseaseUnited States
-
Indiana UniversityNational Institute on Aging (NIA); Regenstrief Institute, Inc.Completed
-
Lady Davis InstituteCanadian Institutes of Health Research (CIHR); Unité de Soutien SSA QuébecRecruitingCritical Care | Family Engagement | VirtualCanada