Patient-Centered Chronic Pain Care

Description

This study will adapt and scale existing AHRQ-supported interoperable CDS for patient-centered chronic pain care. The objective of this project is to study the adaptation and implementation of an existing interoperable CDS tool for pain treatment shared decision making, with tailored implementation support, in primary care clinical settings. The central hypothesis is that tailored implementation support will increase CDS adoption and shared decision making.

Conditions

Chronic Pain, Opioid Use, Musculoskeletal Pain

Study Overview

Study Details

Study overview

This study will adapt and scale existing AHRQ-supported interoperable CDS for patient-centered chronic pain care. The objective of this project is to study the adaptation and implementation of an existing interoperable CDS tool for pain treatment shared decision making, with tailored implementation support, in primary care clinical settings. The central hypothesis is that tailored implementation support will increase CDS adoption and shared decision making.

Scaling Interoperable Clinical Decision Support for Patient-Centered Chronic Pain Care

Patient-Centered Chronic Pain Care

Condition
Chronic Pain
Intervention / Treatment

-

Contacts and Locations

Jacksonville

UF Health Family Medicine - Commonwealth, Jacksonville, Florida, United States, 32254

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Primary care patients receiving care at a participating clinic
  • * Patients with chronic non-cancer musculoskeletal pain and with a recent history of opioid use
  • * Due to the fact that the clinical decision support tool is currently available in English only, non-English speaking patients will not be eligible to participate

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Florida,

Christopher Harle, Ph.D., PRINCIPAL_INVESTIGATOR, University of Florida

Study Record Dates

2025-08-31