A Thematic Analysis of Compassion Rounds
A Thematic Analysis of the Effects of Compassion Rounds on Clinicians and the Families of NICU Patients
1 other identifier
observational
30
1 country
1
Brief Summary
The primary objective of this thematic analysis is to understand the experience of "Compassion Rounds" for patients, families, friends, and clinicians. The secondary objective of this study is to evaluate and interpret data to determine best practice recommendations for standardization and scalability.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 15, 2018
CompletedFirst Posted
Study publicly available on registry
August 28, 2018
CompletedStudy Start
First participant enrolled
October 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
August 28, 2019
CompletedMay 6, 2021
May 1, 2021
10 months
August 15, 2018
May 5, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Validated Thematic Framework to Explain the Effects of Compassion Rounding
Analysis of data collected throughout the study will result in a validated theoretical framework to understand and explain the psychosocial processes that influence participant experience and reported outcomes.
five months
Secondary Outcomes (1)
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
five months
Study Arms (5)
Physicians
interview physicians who have conducted compassion rounds
Chaplains
interview chaplains who have conducted compassion rounds
Other Healthcare Providers
interview other healthcare providers who have conducted compassion rounds
Patients
interview patients who have participated in compassion rounds
Patient family members/friends
interview patient's loved ones who have participated with the patient in compassion rounds
Interventions
Initial interview and potential follow-up interviews and focus group with Florida Hospital employees. Interview participants in compassion rounds
Eligibility Criteria
Participants will be recruited from participants in compassion rounding, including patients, their loved ones, physicians, chaplains, social workers, nurses, and other care providers.
You may qualify if:
- An employee of Florida Hospital or Adventist Health System, or a physician with privileges there, or a patient, or a family or friend who has participated in compassion rounding at a Florida Hospital critical care unit
- Over the age of 18
- Able to provide informed consent
- Must speak and understand English
- Willing and able to provide a contact phone number
You may not qualify if:
- \. Discernible cognitive impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- AdventHealthlead
Study Sites (1)
AdventHealth Orlando
Orlando, Florida, 32804, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kim McManus, Ph.D.
FH Center for CREATION Health Research
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 15, 2018
First Posted
August 28, 2018
Study Start
October 1, 2018
Primary Completion
July 31, 2019
Study Completion
August 28, 2019
Last Updated
May 6, 2021
Record last verified: 2021-05
Data Sharing
- IPD Sharing
- Will not share