Stakeholder Assessment of Implementing the Commission on Cancer Operative Standards for Cancer Surgery
4 other identifiers
observational
31
1 country
1
Brief Summary
This study investigates the barriers to implementing breast Synoptic Operative Reports. Information from this study may help researchers identify performance objectives for the breast Synoptic Operative Reports to be adopted, implemented and continued.
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 Dec 2021
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
Study Start
First participant enrolled
December 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2022
CompletedFirst Submitted
Initial submission to the registry
October 12, 2022
CompletedFirst Posted
Study publicly available on registry
October 18, 2022
CompletedMarch 2, 2023
February 1, 2023
7 months
October 12, 2022
February 28, 2023
Conditions
Outcome Measures
Primary Outcomes (2)
Barriers to implementing breast Synoptic Operative Reports
This is a qualitative study in which we will conduct in-depth, semi-structured interviews with key stakeholders. A template analysis identifying priori themes will be used, then coding for impact and/or implementation strategy.
Up to 2 years
Performance objectives for the breast Synoptic Operative Reports to be adopted, implemented, and continued
This is a qualitative study in which we will conduct in-depth, semi-structured interviews with key stakeholders.A template analysis identifying priori themes will be used, then coding for impact and/or implementation strategy.
Up to 2 years
Study Arms (1)
Observational (interview)
Participants participate in interview over 30-60 minutes.
Interventions
Eligibility Criteria
Key stakeholders (e.g. electronic medical record \[EMR\] engineer, Cancer Liaison Physician \[CLP\], breast surgeon, and cancer registrar administrator) from Ohio State University and 3 other Commission on Cancer (CoC)-accredited cancer programs
You may qualify if:
- Adults \>= 18 years
- Available phone or device for contact
- English speaking
- Works at Commission on Cancer (CoC) - accredited cancer program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ko Un Park, MD
Ohio State University Comprehensive Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
October 12, 2022
First Posted
October 18, 2022
Study Start
December 1, 2021
Primary Completion
June 15, 2022
Study Completion
June 15, 2022
Last Updated
March 2, 2023
Record last verified: 2023-02
Data Sharing
- IPD Sharing
- Will not share