NCT03648866

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Oct 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 15, 2018

Completed
13 days until next milestone

First Posted

Study publicly available on registry

August 28, 2018

Completed
1 month until next milestone

Study Start

First participant enrolled

October 1, 2018

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2019

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 28, 2019

Completed
Last Updated

May 6, 2021

Status Verified

May 1, 2021

Enrollment Period

10 months

First QC Date

August 15, 2018

Last Update Submit

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

Other: interview

Chaplains

interview chaplains who have conducted compassion rounds

Other: interview

Other Healthcare Providers

interview other healthcare providers who have conducted compassion rounds

Other: interview

Patients

interview patients who have participated in compassion rounds

Other: interview

Patient family members/friends

interview patient's loved ones who have participated with the patient in compassion rounds

Other: interview

Interventions

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees. Interview participants in compassion rounds

ChaplainsOther Healthcare ProvidersPatient family members/friendsPatientsPhysicians

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

AdventHealth Orlando

Orlando, Florida, 32804, United States

Location

MeSH Terms

Interventions

Interviews as Topic

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Kim McManus, Ph.D.

    FH Center for CREATION Health Research

    PRINCIPAL INVESTIGATOR

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

Locations