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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05808127
Other study ID # HS-22-00517
Secondary ID 3P30AG024968-20S
Status Completed
Phase N/A
First received
Last updated
Start date August 9, 2023
Est. completion date May 9, 2024

Study information

Verified date May 2024
Source University of Southern California
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients on long-term opioid therapy are aging and now face magnified risk of harm with continued high-dose opioid use. These increased risks are due to age-related changes in drug metabolism, multi-morbidity, and polypharmacy. The dominant approach to mitigate these risks is to screen for aberrant patient opioid behaviors so that clinicians can pre-empt misuse early through review of contractual opioid agreements or by lowering patient dosages. By focusing on opioid misuse alone, this strategy encourages forced opioid tapering that is associated with opioid overdose and mental health crisis. Directing clinician attention to the comorbid conditions associated with opioid misuse may promote safer and more effective care. The objective of this study is to assess the comparative effectiveness of PainTracker, a set of questions that targets a broad range of problems associated with pain, in a randomized controlled trial involving 300 Northwestern Medicine clinicians treating Chronic Opioid Use Registry patients (n=5159).


Description:

Using the electronic health record, patient portal, and patient-reported outcome capabilities, the investigators will develop programming logic for a randomized experimentation platform wherein two or more versions of pain surveys may be delivered to patients. This system will be used to evaluate PainTracker, delivered to half of the sample (approximately 2,579 patients). Clinicians treating Chronic Opioid Use Registry patients that meet the inclusion criteria will be assigned to one of two conditions involving patient surveys: 1) Current Opioid Misuse Measure [COMM] [standard clinical care] or 2) COMM + PainTracker. Surveys will be delivered monthly and patients will be prompted 3 times to complete the survey; once completed, patients will receive a score also delivered to their physician's inbox in Epic.


Recruitment information / eligibility

Status Completed
Enrollment 286
Est. completion date May 9, 2024
Est. primary completion date May 9, 2024
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: • Patients age 65 or older on long-term opioid therapy within the Northwestern Medicine Chronic Opioid Use registry system with at least one primary care encounter in the past 12 months. Exclusion criteria: • Patient visits with active cancer diagnoses

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
PainTracker
The PainTracker tool reframes the patient visit around improving functional status and obtaining functional goals, understanding psychological concerns that may exacerbate pain such as traumatic stress, anxiety, and depression. This approach may promote an increase in referrals for physical therapy, mental health counseling, and psychiatric follow-up.

Locations

Country Name City State
United States Northwestern Medicine Chicago Illinois

Sponsors (4)

Lead Sponsor Collaborator
University of Southern California National Institute on Aging (NIA), Northwestern University, University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Referral rate to non-opioid care Patient referral rate to non-opioid care that includes mental and behavioral health care, physical therapy, or sleep medicine referrals 9 months
Primary Antidepressant orders Rate of orders for antidepressant medications 9 months
Secondary Clinician monthly milligram morphine equivalent (MME) Clinician aggregate monthly milligram (mg) morphine equivalent (ME) for >50 mg ME daily dose visits 9 months
Secondary Benzodiazepine prescribing Clinician aggregate monthly milligram (mg) valium equivalent (VE) for >50 mg VE daily dose visits 9 months
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