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Paired Promotion of Colorectal Cancer and Social Determinants of Health Screening

Primary Purpose

Colorectal Cancer, Social Determinants of Health

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Paired Screening Intervention
Sponsored by
Harvard School of Public Health (HSPH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Colorectal Cancer focused on measuring implementation science, colorectal cancer screening, social determinants of health screening

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Study participants include community health center staff participating in interviews about the implementation of the intervention. Up to four community health center staff members at each of the four community health centers will participate in key informant interviews twice per year. Patients will receive the paired screening intervention as part of their routine care and will not be individually recruited for the study because the intervention is being offered as part of routine care.

Staff Participants

Inclusion Criteria:

  • Staff from community health centers who facilitate screening
  • Age 18 and older

Exclusion Criteria:

  • Have not participated in the implementation of the paired screening intervention

Sites / Locations

  • Harbor Health Services
  • Brockton Neighborhood Health Center
  • Lowell Community Health Center
  • Manet Community Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Paired Screening Intervention

Usual Care Control

Arm Description

In this stepped wedge design, all sites have a period of being in usual care, and then providing the Paired Screening Intervention. Sites serve as their own controls in this design.

Outcomes

Primary Outcome Measures

Conditional Odds Ratio of Patients Screened for Colorectal Cancer During Intervention Compared to Patients Screened During Usual Care
Colorectal cancer screening completion by any guideline-based method. Adjusting for patient socio-demographics, comorbidities, number of healthcare visits, and secular trend. Documented screening in EHR for patients unscreened at the beginning of the step.
Conditional Odds Ratio of Patients Screened for Social Needs During Intervention Compared to Patients Screened During Usual Care
Completion of social needs screening (collected as part of routine clinical care). Adjusting for patient socio-demographics, comorbidities, number of healthcare visits, and secular trend. Documented screening in EHR for patients unscreened at the beginning of the step.

Secondary Outcome Measures

Number of FIT Kits Mailed
Adoption measured by number of FIT kits mailed to patients. Data were summed to calculate a single value.
Number of Reminders Per FIT Mailing
Adoption measured by number of reminders per FIT mailing to patients. Data were summed to calculate a single value.
Number of Reminders Per FIT Return
Adoption measured by number of reminders per FIT returned. Data were summed to calculate a single value.

Full Information

First Posted
September 30, 2020
Last Updated
July 31, 2023
Sponsor
Harvard School of Public Health (HSPH)
Collaborators
National Institutes of Health (NIH), National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT04585919
Brief Title
Paired Promotion of Colorectal Cancer and Social Determinants of Health Screening
Official Title
Paired Promotion of Colorectal Cancer and Social Determinants of Health Screening
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
January 25, 2022 (Actual)
Study Completion Date
January 25, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Harvard School of Public Health (HSPH)
Collaborators
National Institutes of Health (NIH), National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This work is an implementation science study that examines different aspects of implementing a single intervention. The intervention consists of asking community health centers to implement an outreach strategy to screen patients for colorectal cancer and for social determinants of health in community health centers at the same contact point. These are both clinical targets that the CHCs feel that their patients need and want to offer at a higher rate. The intervention consists of outreach to patients in need of colorectal cancer screening (CRC) to offer fecal immunochemical test (FIT) screening and screening for social determinants of health (SDOH). In this implementation science study, the intervention is an evidence-based intervention being implemented in real-world clinical practice. The intervention is the outreach to offer FIT and SDOH, conducted by clinic staff. Both evidence-based screening activities-FIT and SDOH screening-are used in the practices included in the study but pairing them is intended to increase efficiency and patient-centeredness by addressing health related social needs that may impact patients' ability to engage in cancer screening. The study aims to test the effect of implementing the intervention on clinical and process outcomes. Clinical outcomes are CRC screening and SDOH screening. Analysis of process outcomes includes measuring what organizational factors influence implementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Social Determinants of Health
Keywords
implementation science, colorectal cancer screening, social determinants of health screening

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
This trial uses a randomized stepped wedge study design. This pragmatic design involves a sequential, randomized roll-out of the intervention across the four participating clinical sites or "clusters" over 8 week intervals or "steps." The intervention is the paired outreach to patients in need of CRC screening to offer FIT screening and screening for SDOH. The participants who will be enrolled are CHC staff who will provide input on the implementation processes and outcomes.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Paired Screening Intervention
Arm Type
Experimental
Arm Title
Usual Care Control
Arm Type
No Intervention
Arm Description
In this stepped wedge design, all sites have a period of being in usual care, and then providing the Paired Screening Intervention. Sites serve as their own controls in this design.
Intervention Type
Behavioral
Intervention Name(s)
Paired Screening Intervention
Intervention Description
The intervention is the implementation of a paired outreach strategy to patients in need of colorectal cancer screening to offer FIT testing and to complete screening for social determinants of health. These screening activities are part of routine practice but the intervention that is being implemented is the paired outreach for both CRC screening and SDOH screening.
Primary Outcome Measure Information:
Title
Conditional Odds Ratio of Patients Screened for Colorectal Cancer During Intervention Compared to Patients Screened During Usual Care
Description
Colorectal cancer screening completion by any guideline-based method. Adjusting for patient socio-demographics, comorbidities, number of healthcare visits, and secular trend. Documented screening in EHR for patients unscreened at the beginning of the step.
Time Frame
13 pre implementation months, 14 post-implementation months
Title
Conditional Odds Ratio of Patients Screened for Social Needs During Intervention Compared to Patients Screened During Usual Care
Description
Completion of social needs screening (collected as part of routine clinical care). Adjusting for patient socio-demographics, comorbidities, number of healthcare visits, and secular trend. Documented screening in EHR for patients unscreened at the beginning of the step.
Time Frame
13 pre implementation months, 14 post-implementation months
Secondary Outcome Measure Information:
Title
Number of FIT Kits Mailed
Description
Adoption measured by number of FIT kits mailed to patients. Data were summed to calculate a single value.
Time Frame
4 months post-implementation, 8 months post-implementation
Title
Number of Reminders Per FIT Mailing
Description
Adoption measured by number of reminders per FIT mailing to patients. Data were summed to calculate a single value.
Time Frame
4 months post-implementation, 8 months post-implementation
Title
Number of Reminders Per FIT Return
Description
Adoption measured by number of reminders per FIT returned. Data were summed to calculate a single value.
Time Frame
4 months post-implementation, 8 months post-implementation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Study participants include community health center staff participating in interviews about the implementation of the intervention. Up to four community health center staff members at each of the four community health centers will participate in key informant interviews twice per year. Patients will receive the paired screening intervention as part of their routine care and will not be individually recruited for the study because the intervention is being offered as part of routine care. Staff Participants Inclusion Criteria: Staff from community health centers who facilitate screening Age 18 and older Exclusion Criteria: Have not participated in the implementation of the paired screening intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen Emmons, PhD
Organizational Affiliation
Harvard TH Chan School of Public Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harbor Health Services
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02122
Country
United States
Facility Name
Brockton Neighborhood Health Center
City
Brockton
State/Province
Massachusetts
ZIP/Postal Code
02301
Country
United States
Facility Name
Lowell Community Health Center
City
Lowell
State/Province
Massachusetts
ZIP/Postal Code
01854
Country
United States
Facility Name
Manet Community Health Center
City
Quincy
State/Province
Massachusetts
ZIP/Postal Code
02171
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported here, after deidentification (text, tables, figures, and appendices). Upon request and appropriate approvals.
IPD Sharing Time Frame
6 months after publication, and for 3 years.
IPD Sharing Access Criteria
Outside investigators will need an approved concept proposal to analyze study data and spend the requisite time with study staff to learn about the data elements needed to conduct the proposed analysis. With the assistance of our analytic team, s/he will draft a detailed analysis plan and present to the core group of co-investigators. The discussion at this meeting ensures adequate knowledge of the data, and the presenter gains much insight into how the analysis can be most useful and how it relates to previous analyses. Once the plan is approved by this group, it must also be approved by the CHCs that provide the de-identified data. Following approval by the appropriate IRBs and confirmation that it meets HIPAA requirements, s/he may sign a DUA to use a secure, de-identified dataset to complete only the approved analyses and write the manuscript(s) offsite. A formal data analysis plan application and DUA are still in development. Requests should be directed to jdaly@hsph.harvard.edu.
Citations:
PubMed Identifier
36194312
Citation
Aschbrenner KA, Kruse G, Emmons KM, Singh D, Barber-Dubois ME, Miller AM, Thomas AN, Bartels SJ. Stakeholder and Equity Data-Driven Implementation: a Mixed Methods Pilot Feasibility Study. Prev Sci. 2022 Oct 4:1-11. doi: 10.1007/s11121-022-01442-9. Online ahead of print.
Results Reference
derived

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Paired Promotion of Colorectal Cancer and Social Determinants of Health Screening

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