Skip to main content
Clinical Trials/NCT02746354
NCT02746354
Completed
Not Applicable

Effects of a Patient Driven Assessment Process With Complex Pain Patients (PDAP)

Kaiser Permanente1 site in 1 country100 target enrollmentOctober 2012
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Kaiser Permanente
Enrollment
100
Locations
1
Primary Endpoint
Pain severity and functioning
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The objective of this study is to engage patients with chronic pain and other key stakeholders in an iterative process of pilot-testing a validated patient generated instrument, the Measure Yourself Medical Outcome Profile (MYMOP), to support primary care encounters and provide a direct comparison between a strategy of incorporating patient reported outcomes into the package of care for complex pain patients and usual care. The specific aims of this phase of the project are to: 1) adapt the MYMOP for use in the primary care setting well-integrated into everyday practice flow, and 2) evaluate whether the utilization of the MYMOP data in routine primary care encounters results in improvements in patient symptoms and functioning over time as well as increased satisfaction with the visit for patients and primary care providers. To achieve Aim 2, the investigators will compare the reported outcomes and health care utilization from participating patients in this study for whom the MYMOP-based instrument will be used in routine clinical care to a matched group of chronic pain patients who will not receive the MYMOP-based assessment but will otherwise have similarly collected data. This also allows us to evaluate of the extent to which use of the tool adds patient-centered information to more conventional instruments. In addition to these two aims, for a third aim, the investigators plan to collect qualitative data from patients, their family members, Kaiser Permanente Northwest (KPNW) health care providers, and KPNW administrators to better understand the needs of this subpopulation of patients.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
April 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years or older
  • Kaiser Permanente Northwest health plan members with at least 12 months of continuous eligibility at time of study entry and receive primary care from participating physicians
  • Continued opioid use during the previous 6 months, as defined by 2 or more dispenses of long-acting opioids and/or a minimum cumulative supply of 90 days' worth of short-acting opioids based on electronic medical record (EMR) d) EMR recorded diagnosis of nonspecific chronic pain, Fibromyalgia, or diagnosis of ≥ 2 types of pain in the past year

Exclusion Criteria

  • Active cancer
  • Substance abuse or dependence
  • Hospice care
  • Severe mental illness

Outcomes

Primary Outcomes

Pain severity and functioning

Time Frame: Change at 5 months, change from 5 to10 months and change at 10 months

Brief Pain Inventory (BPI-SF): pain severity and pain interference subscales

Secondary Outcomes

  • Patient skill in managing health care(Change at 5 months, change from 5 to10 months and change at 10 months)
  • Quality of sleep(Change at 5 months, change from 5 to10 months and change at 10 months)
  • Clinician empathy(Change at 5 months, change from 5 to10 months and change at 10 months)
  • Health-related quality of life(Change at 5 months, change from 5 to10 months and change at 10 months)
  • Self-care practices(Change at 5 months, change from 5 to10 months and change at 10 months)
  • Health services utilization(Change at 5 months, change from 5 to10 months and change at 10 months)

Study Sites (1)

Loading locations...

Similar Trials