Anxiety Clinical Trial
Official title:
Controlled Substance Treatment Agreements in an Internal Medicine Residents' Clinic
Verified date | September 2015 |
Source | Ohio State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this study is to characterize and improve controlled substance, carisoprodol
and tramadol use in an internal medicine residents' clinic. Specific objectives of this
study include:
- To measure the adherence to a controlled substance treatment agreement (CSTA) before
and after implementation of a population management intervention
- To determine the number of patients on a CSTA with a discrepancy identified on a urine
drug screen or an Ohio Automated Rx Reporting System (OARRS) report
- To track the number of patients on a morphine equivalent dose (MED) of ≥ 80 mg/day
before and after implementation of a review intervention
- To characterize the healthcare utilization of patients taking controlled substances,
carisoprodol, or tramadol by tracking the mean number of ED visits, hospital
admissions, telephone calls, and clinic office visits during a 6 month period
Status | Completed |
Enrollment | 96 |
Est. completion date | March 2015 |
Est. primary completion date | January 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 years and older - Residents and attending physicians who work in the resident continuity practice Exclusion Criteria: - Age < 18 years of age |
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
United States | The Ohio State University | Columbus | Ohio |
Lead Sponsor | Collaborator |
---|---|
Ohio State University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of Patients Adhering to Controlled Substance Agreement | To measure the adherence to a controlled substance treatment agreement (CSTA) before and after implementation of a population management intervention | 18 months | No |
Secondary | Discrepancy on urine drug screen | To determine the number of patients on a CSTA with a discrepancy identified on a urine drug screen or an Ohio Automated Rx Reporting System (OARRS) report | 18 months | No |
Secondary | Morphine Equivalent Review | To track the number of patients on a morphine equivalent dose (MED) of = 80 mg/day before and after implementation of a review intervention | 18 months | No |
Secondary | Healthcare Utilization | To characterize the healthcare utilization of patients taking controlled substances, carisoprodol, or tramadol by tracking the mean number of ED visits, hospital admissions, telephone calls, and clinic office visits during a 6 month period | 18 months | No |
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