Using Implementation Science to Adapt a Targeted Transportation Intervention for Patients With Diabetic Retinopathy (PRONTO-EYE)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Illinois at Chicago

About this trial

This is a a type 3 hybrid effectiveness-implementation pilot study to evaluate the PRONTO-EYE intervention, a rideshare transportation program, in patients with diabetic retinopathy with Medicaid insurance on adherence to ophthalmology visits.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Established patient

Medicaid insurance

History of diabetic retinopathy

Lives within 25 miles of the clinic

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • PRONTO-EYE

    Behavioral

    The PROgram for Non-emergency TranspOrtation (PRONTO) - EYE intervention is a rideshare transportation program designed for patients to get to and from their visits. The intervention includes the rideshare as well as a service blueprint of the offering and how all individuals in the health system interact with it.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: PRONTO-EYE rideshare intervention offeredExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Number of patients that adhere to their scheduled ophthalmology visits

Proportion of patients who attend their scheduled ophthalmology visit compared to pre-implementation historical controls.

Time frame
Baseline up to 6 months

Secondary outcomes

1

Adoption of PRONTO-EYE

Uptake and intention to employ the innovation, including percentage of patients who opt into rideshare and stakeholder buy-in, assessed via EHR data and interviews.

Time frame
Assessed continuously throughout the up to 6-month feasibility trial, with a final summary at trial completion.
2

Appropriateness of PRONTO-EYE

Perceived fit, relevance, or compatibility of the intervention for the clinic's mission and patient needs, measured using questions adapted from the Intervention Appropriateness Measure (IAM) survey and interviews.

Time frame
Implementation outcomes will be assessed throughout the duration of the study
3

Feasibility of PRONTO-EYE

The number of rides successfully completed divided by the number of rides scheduled, as assessed via ride logs and observation.

Time frame
Assessed upon completion of the up to 6-month feasibility trial
4

Fidelity of PRONTO-EYE

Degree to which the PRONTO-EYE transportation intervention was implemented as originally proposed, including adherence to planned processes for ride scheduling, patient eligibility criteria, and staff roles. Assessed via EHR data, program logs, and semi-structured interviews with staff.

Time frame
Assessed continuously throughout the up to 6-month feasibility trial, with a final summary at trial completion.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Illinois at Chicago

Lead sponsor

National Eye Institute (NEI)

Collaborator