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Home Visits for Patients at Risk for Appointment No-shows (SNAP HOME)

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Johns Hopkins University

Status

Withdrawn

Conditions

No-Show Patients
Utilization, Health Care
Engagement, Patient

Treatments

Other: Home visit

Study type

Interventional

Funder types

Other

Identifiers

NCT04376736
IRB00196142

Details and patient eligibility

About

Unused clinic visits due to patient no-shows continue to plague American healthcare as a large source of waste and avoidable constraint on access. The average no-show rate across 105 studies was 23% though with wide variation (4% to 79%). No-show behavior has adverse effects on patients, providers, and healthcare organizations' operational and financial outcomes. Patients that miss clinic visits are more likely to need acute care and suffer poor health outcomes. There have been increasingly sophisticated efforts focused on predicting which patients are likely to no-show. This can allow for tactful over-booking and/or patient outreach. At Hopkins, investigators have implemented a novel machine learning based approach for identifying those patients at high-risk for no-show. Offering home visits for patients who are most likely to no-show is an appealing strategy to connect medical providers with patients who need care but are otherwise unlikely to receive it. Yet, it is unclear if this would be helpful to engage patients in their care, and encourage subsequent attendance, or if it would encourage future missed appointments, fostering a reliance on possible ongoing home visits. This study would link existing efforts with no-show prediction to home visits by internal medicine residents and evaluate its clinical impact. Patients at high-risk for no-show will be randomized into the control arm where patients will be called to remind patients of their visits. Those randomized into the intervention arm will be offered a one time home visit in lieu of their in-person visit to help understand barriers to in-person care and build rapport. Outcomes evaluated include future in-person show rates and healthcare cost/utilization

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • One or more poorly controlled chronic medical illness
  • More than one chronic illness, regardless of its level of control
  • Acute illness

Exclusion criteria

  • No documented medical illnesses (acute or chronic)
  • Single well controlled chronic illness

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Control arm
No Intervention group
Description:
Patients are reminded about their appointments
Intervention arm
Experimental group
Description:
Patients are offered a one-time home visit by providers in lieu of their upcoming in-person visit
Treatment:
Other: Home visit

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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