N/A
N=1,525
The Effect of Informative Letters on the Prescription and Receipt of Schedule II Controlled Substances
Economics · Fraud · Delivery of Health Care · Health Expenditures · Centers for Medicare and Medicaid Services (U.S.)
Bottom Line
View on ClinicalTrials.gov: NCT02345434 ↗Enrolled (actual)
1,525
Serious AEs
0.0%
Results posted
Nov 2021
Primary outcome: Primary: 30-day Equivalent Prescribing of Schedule II Controlled Substances — 461.1; 450.0 30-day equivalent prescription fills
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Informative letter (Other)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- Abdul Latif Jameel Poverty Action Lab
- Primary completion
- Aug 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY 30-day Equivalent Prescribing of Schedule II Controlled Substances |
— | — |
| SECONDARY 30-day Equivalent Prescribing of Schedule II Controlled Substances |
— | — |
| SECONDARY 30-day Equivalent Prescribing of Schedule II Controlled Substances |
— | — |
| SECONDARY 30-day Equivalent Prescribing of Schedule II Controlled Substances |
— | — |
| SECONDARY 30-day Equivalent Prescribing of Schedule II Controlled Substances |
— | — |
Summary
Fraud and waste is estimated to cost the American health care system nearly $200 billion each year, and the public Medicare and Medicaid programs about $60 billion each year. This study will evaluate a new method for fighting fraud: mailing informative letters to outlier providers to notify them of their aberrant behavior. These letters are targeted at high prescribers of schedule II controlled substances in Medicare Part D. The investigators will look at the effects of these letters on the behavior of providers and their patients. These effects are of substantial policy interest as they suggest how to best design anti-fraud policies. They are also of academic interest, shedding light on the behavior of physicians and their patients.
Eligibility Criteria
Inclusion Criteria
- Outlier with respect to the count of schedule II prescription drug events relative to peer group of prescribers in two of the three years 2011, 2012, and 2013
- Outlier with respect to the 30-day equivalent prescriptions of schedule II substances relative to peer group of prescribers in two of the three years 2011, 2012, and 2013
Exclusion Criteria
- Deceased
Data sourced from ClinicalTrials.gov (NCT02345434). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.