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Table 1 Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) areas of inquiry of the SAFER protocol pilot trial

From: Developing and evaluating a SAFER model to screen for diabetes complications among people experiencing homelessness: a pilot study protocol

Reach

Effectiveness

Adoption

Implementation

Maintenance

How many participants were willing to participate in the study? How many people declined participation in the study?

Data sources: consent to contact forms and qualitative interviews with service providers

Primary objective: What is the incremental increase in the completion of comprehensive screening and glycemic monitoring?

Data sources: chart review, participant clinical record

What challenges did facilities face in the process of implementing the intervention?

Data sources: qualitative interviews with service providers

Was the intervention delivered consistently?

Data sources: field notes

What were the barriers to continuing this program after completion of the pilot trial, as described by service providers?

Data sources: qualitative interviews with service providers

Of those who agreed to participate, how many attended both the baseline and the follow-up sessions?

Data sources: participant clinical record

How many participants with complications, detected as a result of the screening intervention, were referred to a specialist for follow-up care?

Data sources: participant clinical record and field notes

According to both participants and providers, was the intervention well received?

Data sources: qualitative interviews with service providers and participants

Was it feasible to deliver the intervention in the allotted time frame?

Data sources: field notes

According to the participants, would they continue attending the screening intervention on a yearly basis if it became a permanent program?

Data sources: qualitative interviews with participants

What were the clinical and sociodemographic characteristics of the participants?

Data sources: baseline questionnaire and participant clinical record

How many participants attended specialist referral appointments?

Data sources: participant clinical record and field notes

 

Was the intervention delivered as intended?

Data sources: field notes

Did partnering facilities continue to deliver the intervention after the pilot trial was complete? Why or why not?

Data sources: qualitative interviews with service providers

What was the incremental increase in specialist visits for participants requiring follow-up care?

Data sources: chart review, participant clinical record

 

How many participants attended both visits with the CRN?

Data sources: Participant clinical record

What proportion of service providers indicated a willingness to deliver the intervention after the conclusion of the pilot trial? What were their motivations for wanting to do that?

Data sources: qualitative interviews with service providers

What were the participants’ experiences with the program?

Data sources: qualitative interviews with participants

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