CMSL Ambulatory Sensitive Condition Nudge Study 2

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30+
SponsorGeisinger Clinic

About this trial

The project aims to evaluate a nurse-led intervention to reduce inappropriate emergency department (ED) use among adult patients seen at Geisinger's Community Medicine Service Line (CMSL) clinics. The intervention occurs immediately following an appointment where a patient receives a diagnosis of an ambulatory sensitive condition (ASC; i.e., a condition considered to be a risk factor for near-term ED use). The evaluation will compare eligible patients with an ASC who were randomly assigned to receive follow-up outreach (patient portal message and/or call) from a nurse (who was automatically prompted via the Epic electronic health record system to initiate outreach) with those who were randomly assigned to receive standard care. Analyses will be intent-to-treat. The primary outcome is ED use in the week (i.e., 7 days) following the appointment.

We ran an earlier version of this intervention (NCT06798389). The current study is modified based on results and clinical guidance. Specifically, more conditions will be included as qualifying ASCs for enrollment. Patients under 30 will be excluded. And rather than calling all patients as in the original study, patient portal users may be contacted via the portal instead of or in addition to a phone call. Finally, in the first study, the intervention was differentially effective by age group (\<45, 45-64, 65+). Our primary analysis will be conducted separately by age group, though we will also conduct an analysis combining across age groups.

We will run the study until we reach at least 4,330 patients in each of the following age groups: patients aged 30-45, patients aged 45-64, patients aged 65+. Therefore, our estimated sample size is at least 4,330x3 = 12,990.

We may be required to do an interim data pull and/or stop the study early at the direction of clinical or operational leaders.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 30 years +

Has a qualifying visit in CMSL with an ambulatory sensitive condition (ASC) encounter diagnosis

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nurse Nudge

    Behavioral

    Nurses will be nudged to contact patients, which may increase the likelihood that the patient receives a post- appointment follow-up call and/or portal message.

Treatment groups

12,990 Participants
are divided into 2 treatment groups
Group A: Nurse NudgeExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

ED Visit (yes/no)

Visited the ED (y/n)

Time frame
within 7 days post-appointment

Secondary outcomes

Other outcomes

1

Nurse call to patient

Nurse calls patient (y/n)

Time frame
Within 7 days post-appointment
2

Nurse message to patient

Nurse sends MyChart message to patient (y/n)

Time frame
Within 7 days post-appointment
3

Nurse calls or sends message to patient

Nurse calls or sends MyChart message to patient (y/n)

Time frame
Within 7 days post-appointment

Sponsors and contacts

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