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Completed

NCT Number: NCT02345434

The Effect of Informative Letters on the Prescription and Receipt of Schedule II Controlled Substances

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Informative letter

Other

The intervention is a letter that describes the Schedule II prescribing activity of the individual in comparison to a peer group of similar prescribers. It highlights the fact that the prescriber's activity is highly unlike her peers.

Other names: Comparative billing report, Peer activity report

Primary outcomes

  1. 30-day Equivalent Prescribing of Schedule II Controlled Substances

    Time frame: 3 months

    The prescribing of schedule II controlled substances over the 3 months following the initial sending of the letters. Prescribing is defined as the total "days supply" of schedule II controlled substances attributed to the prescriber, expressed in "30-day equivalents" i.e. divided by 30.

Secondary outcomes

  1. 30-day Equivalent Prescribing of Schedule II Controlled Substances

    Time frame: 1 month

  2. 30-day Equivalent Prescribing of Schedule II Controlled Substances

    Time frame: 6 months

  3. 30-day Equivalent Prescribing of Schedule II Controlled Substances

    Time frame: 9 months

  4. 30-day Equivalent Prescribing of Schedule II Controlled Substances

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Abdul Latif Jameel Poverty Action Lab

Other

Collaborators

  • Centers for Medicare and Medicaid Services
  • General Services Administration (GSA)

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jan 26, 2015
Registry last updated
Nov 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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