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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02923024
Other study ID # 825856
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 2017
Est. completion date December 2018

Study information

Verified date December 2018
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Oscar spends a significant amount of money every year on high cost high need individuals. With this increase in health care spending, Oscar Health is looking to expand care post emergency room and inpatient utilization for their members. In order to reduce hospital readmissions, reduce emergency room utilization, and increase the overall health of their members, Oscar is investing in a program to bring members better care through increased engagement with their primary care physician.


Description:

Using their existing technology, Oscar is employing a randomized controlled trial among their physicians to improve their engagement and relationships with patients. The goal will be to test and refine patient pings as a provider engagement tool, with an eye toward using it within the broader approach to high-risk patients as well. The Penn team is helping to design the intervention, which includes helping with determining what the three arms will be and randomizing physicians and practice sites. They will implement a three-arm trial with the first arm being usual care (no pings), the second arm being the intervention of information, and the third arm being the intervention of information and financial incentives. In the two intervention groups, providers will be sent patient pings after a patient experiences a trigger event. This trigger event could be an emergency room visit, admission to a hospital, or a hospital discharge event. The patient ping will be sent to the patients doctors including primary care physicians and specialists. If the patient does not have a doctor, a ping will not be sent. In the third arm, physicians will be incentivized to see patients immediately via phone call or in office visit. Physicians will receive an incentive for calling the member within 48 hours of trigger event and will receive a larger financial incentive for seeing the patient for an office visit within 7 days of trigger event. This bonus payment will be paid to physicians uncoupled from usual reimbursement as a separate bonus check to increase salience. No pings will be sent to the physicians for the patients randomized to arm 1: usual care.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Primary care and specialist physicians under contract with Oscar Health insurance

Exclusion Criteria:

- Any primary care and specialist physician not under contract with Oscar Health.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Patient Ping
The patient ping will be a fax sent from Oscar Health to physician that will include information on the physician's patient's trigger event and contact information for the physician to reach out to the member.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Pennsylvania Oscar Health Insurance

Outcome

Type Measure Description Time frame Safety issue
Primary Patient office visits with physician The study team will measure the number of patients that saw their physician within seven days of the trigger event and patient ping. Within 7 days of trigger event and patient ping
Primary Physician phone call to patient The study team will measure the number of patients that received a phone call from their physician within 48 hours of trigger event. 48 hours of trigger event and patient ping
Secondary Number of emergency room visits post trigger event The study team will measure emergency room utilization post trigger event. 6 months
Secondary Number of outpatient visits post trigger event The study team will measure outpatient utilization post trigger event. 6 months