Enhancing Electronic Health Systems to Decrease the Burden of Colon Cancer, Lung Cancer, Obesity, Vaccine-Preventable Illness, and LivER Cancer (CLOVER)

December 23, 2023 updated by: University of California, Davis
The purpose of CLOVER is to utilize Epic Healthy Planet to increase adherence to United States Preventive Services Task Force (USPSTF) and Centers for Disease Control and Prevention (CDC) recommendations in adults age 50 and older.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

20000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • California
      • Sacramento, California, United States, 95817
        • UC Davis Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

- Any patient who has a UC Davis or UC Irvine primary care provider (PCP) and is deficient in any of the following: colon cancer screening, lung cancer screening, tobacco cessation counseling, obesity counseling, pneumonia vaccination, shingles vaccine, and hepatitis C screening.

Exclusion Criteria:

- Patients outside of the age limits or have an established PCP.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: CLOVER arm
This arm will contain clinics that utilize the CLOVER intervention
Other: Epic Healthy Planet Population Health Module
Electronic population health module which is tailored to increased adherence to USPSTF and CDC recommendations
No Intervention: Standard of Care arm
This arm will contain clinics that do not utilize the CLOVER intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall Adherence to CLOVER Metrics
Time Frame: 6 months
This is the proportion of patients who appropriately completed screenings and vaccinations that they were eligible for
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Colon cancer screening
Time Frame: 6 months
Proportion of eligible patients who completed colon cancer screening.
6 months
Lung cancer screening
Time Frame: 6 months
Proportion of eligible patients who completed lung cancer screening.
6 months
Tobacco cessation counseling
Time Frame: 6 months
Proportion of eligible patients who completed tobacco cessation counseling.
6 months
Obesity counseling
Time Frame: 6 months
Proportion of eligible patients who completed obesity counseling.
6 months
Pneumonia vaccination
Time Frame: 6 months
Proportion of eligible patients who completed pneumonia vaccination.
6 months
Shingles vaccination
Time Frame: 6 months
Proportion of eligible patients who completed shingles vaccination.
6 months
Hepatitis C screening
Time Frame: 6 months
Proportion of eligible patients who completed hepatitis C screening.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of California, Davis

Collaborators

University of California, Irvine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 5, 2020

Primary Completion (Actual)

October 5, 2022

Study Completion (Actual)

October 5, 2022

Study Registration Dates

First Submitted

August 31, 2020

First Submitted That Met QC Criteria

August 31, 2020

First Posted (Actual)

September 7, 2020

Study Record Updates

Last Update Posted (Actual)

December 27, 2023

Last Update Submitted That Met QC Criteria

December 23, 2023

Last Verified

November 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1624888

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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