Integrating Patient Reported Outcomes (I-PRO) Study for Multidisciplinary Pain Care

NACompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

July 31, 2014

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
Chronic Noncancer Pain
Interventions
OTHER

Providers of Novel Care

Providers in the treatment group will be asked (1) to complete a series of six online education modules in pain care, (2) will be given access to new patient reported outcomes questionnaire data collected from patients within the electronic health record, (3) asked to review this data and related care recommendations during the patient visit, and (4) asked to complete baseline and monthly online surveys related to experiences and satisfaction with providing care to patients with chronic noncancer pain.

OTHER

Providers of Usual Care

Providers in the control group will provide care as usual to patients and will be asked to complete baseline and monthly online surveys related to experiences and satisfaction with providing care to patients with chronic noncancer pain.

Trial Locations (4)

32607

Family Medicine at Hampton Oaks, Gainesville

32608

Family Medicine at Haile Plantation, Gainesville

32641

Eastside Community Practice, Gainesville

32669

Family Medicine at Jonesville, Gainesville

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

University of Florida

OTHER