Eliminating Barriers to Colorectal Cancer Screening Using Rapid Cycle Testing: A Pilot Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMassachusetts General Hospital

About this trial

The investigators will use a mixed methods study i.e. focus groups involving CHC staff as well as quantitative study which involves analyzing data that is available from the EHR and DRVS population management platform.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Staff members at partnering sites (see locations) who are administrative leaders, population health managers, data analysts, quality improvement staff, nurses, nurse managers, practice managers, medical assistants, and providers.

Staff members at partnering sites ages 18+.

Disqualifiers

Staff members that are not involved in CRC screening practices at CHCs.

Trial design

Design model

Sequential

Treatments tested in this trial

  • Implementation Science Strategy

    Behavioral

    The investigators will be conducting focus groups and identifying barriers and facilitators, and the investigators will be matching identified barriers and facilitators to implementation strategies at the patient, provider, and system level which the investigators will be testing using rapid-cycle methods.

Treatment groups

2 Participants
are divided into 2 treatment groups
Group A: Introduction of Implementation StrategiesOther 1 intervention
Group B: Withdrawal of Implementation StrategiesNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Primary Outcome 1: Acceptability of Implementation Strategies

The investigators will measure the acceptability of the implementation strategies determined in Aim 2. This will be measured through a post-implementation survey given to the CHC staff members who participate in systems-level implementation at the two CHC pilot test sites in Aim 3.

Time frame
4 months
2

Primary Outcome 2: Feasibility of Implementation Strategies

The investigators will measure the feasibility of the implementation strategies determined in Aim 2. This will be measured through a post-implementation survey given to the CHC staff members who participate in systems-level implementation at the two CHC pilot test sites in Aim 3.

Time frame
4 months
3

Primary Outcome 3: Appropriateness of Implementation Strategies

The investigators will measure the appropriateness of the implementation strategies determined in Aim 2. This will be measured through a post-implementation survey given to the CHC staff members who participate in systems-level implementation at the two CHC pilot test sites in Aim 3.

Time frame
4 months

Secondary outcomes

1

Secondary Outcome: CRC Screening Rates

The secondary outcomes will be change in colorectal cancer screening rate. This will be measured by the difference in the colorectal cancer screening tests ordered and completed compared to the pre-implementation period.

Time frame
4 months

Other outcomes

Sponsors and contacts

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Massachusetts General Hospital

Lead sponsor

National Cancer Institute (NCI)

Collaborator