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Paired Promotion of Colorectal Cancer and Social Determinants of Health Screening

P

President and Fellows of Harvard College

Status

Completed

Conditions

Social Determinants of Health
Colorectal Cancer

Treatments

Behavioral: Paired Screening Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04585919
67702115
P50CA244433 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Enrollment

26 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

26 participants in 2 patient groups

Paired Screening Intervention
Experimental group
Treatment:
Behavioral: Paired Screening Intervention
Usual Care Control
No Intervention group
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.

Trial documents
1

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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