Quality Improvement Pilot
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Quality Improvement Practice Facilitation Intervention.
- Who it may be relevant to
- Registry conditions: Cancer. Basic parameters: 18 years — 99 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Facilitation of Cancer Prevention and Screening Guideline Implementation: Pilot Study
Overview
The overall goal of this study is to develop and pilot test the use of practice facilitation as an intervention for healthcare providers and staff, with the goal of improving the implementation of cancer prevention and screening guidelines in primary care settings.
Interventions
- Behavioral Quality Improvement Practice Facilitation Intervention
The practice facilitation intervention (implementation strategy package) consists of QI projects designed for primary care providers with external practice facilitation and technical support provided by a QI Coach and Data Coach on our team. The QI projects focus on the implementation of cancer prevention and early detection guidelines in primary care settings, specifically one QI project for each of the following clinical guidelines: colorectal cancer screening, lung cancer screening, and toba
Primary outcome measures
- Colorectal Cancer: Screening Rate (Patient Population) [Time frame: 6 months]
- Lung Cancer: Screening Rate (Patient Population) [Time frame: 6 months]
- Tobacco: Treatment Rate (Patient Population) [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- Normal Volunteers
Exclusion criteria
- None
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 1 center
- University of Kentucky — Lexington
Identifiers
NCT: NCT05415800 · 77178 · 3P30CA177558-08S3