A Survey to Eval the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
NCT ID: NCT02667158
Last Updated: 2020-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
1085 participants
OBSERVATIONAL
2014-11-07
2018-12-19
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of Drug Utilization Patterns for Extended Release/Long Acting Opioids and Comparator Products
NCT02925806
A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department
NCT02665429
Pharmacist for Detecting Opioid Misuse
NCT04544696
A Strategy to Reduce Opioid Drug Prescribing by Clinicians
NCT03809507
Appropriate Opioid Quantities for Acute Pain - Pharmacist Study
NCT04484610
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The objective of PMR Study #2065-4 is to define and validate doctor/pharmacy shopping as outcomes suggestive of misuse, diversion, abuse and/or addiction.
Study #2065-4 consists of three sub-studies, Study 4A, Study 4B, and Study 4C. In the current study (#2065-4 sub-study, Study 4B), the association between doctor/pharmacy shopping behavior and misuse, diversion and abuse will be assessed by surveying patients within the a priori defined four categories of shopping behaviors. The four categories of shopping behaviors identified and defined in Study 4A will be applied to Study 4B. Asking patients directly about their behaviors related to misuse and abuse will provide us with the patient's perspective that is unavailable in Study 4A. Surveying patients regarding misuse and abuse requires the use of an instrument that has undergone a validation process to ensure that misuse and abuse are being measured. Study 4B will utilize the Prescription Opioid Misuse and Abuse Questionnaire (POMAQ) that will be validated in PMR Study #2065-2A. An administrative claims database will be used to identify the eligible patient population using their pharmacy claims for immediate release (IR) or ER/LA opioid analgesics to determine the number of prescribers and number of pharmacies they visit. Consenting patients will be asked to complete an online survey that includes the POMAQ to self-report their behaviors of misuse, abuse and/or diversion. It is hypothesized that as the likelihood of doctor/pharmacy shopping behavior increases the risk of misuse, abuse and/or diversion.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
No shopping behavior
Patients will be grouped into one of the categories based on the most recent 18 months of data available at the time the patient sample is identified
Survey to Eval Relation between Shopping and Misuse, Abuse
A Survey Study to Evaluate the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
Minimal shopping behavior
Patients will be grouped into one of the categories based on the most recent 18 months of data available at the time the patient sample is identified
Survey to Eval Relation between Shopping and Misuse, Abuse
A Survey Study to Evaluate the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
Marked shopping behavior
Patients will be grouped into one of the categories based on the most recent 18 months of data available at the time the patient sample is identified
Survey to Eval Relation between Shopping and Misuse, Abuse
A Survey Study to Evaluate the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
Extensive shopping behavior
Patients will be grouped into one of the categories based on the most recent 18 months of data available at the time the patient sample is identified
Survey to Eval Relation between Shopping and Misuse, Abuse
A Survey Study to Evaluate the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Survey to Eval Relation between Shopping and Misuse, Abuse
A Survey Study to Evaluate the Relation Between Doctor/Pharmacy Shopping and Outcomes Suggestive of Misuse, Abuse and/or Diversion
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Based on claims for the most recent 18 months of data, meet classification criteria for one of the four a priori defined doctor/pharmacy shopping categories.
3. Currently active, commercially-insured, survey eligible with medical and pharmacy benefits with a health plan included in the HealthCore Integrated Research Database (HIRD) at the time the sample list is extracted.
4. At least 18 years of age as of the date of the first IR or ER/LA opioid dispensing in the most recent 18 months of claims data.
5. A telephone number or address known to HealthCore.
Exclusion Criteria
2. Patients with a known history of abuse
3. Patients who do not indicate that they have read about all pertinent aspects of the study and agree to participate.
4. Patients who fail to validate their name and/or date of birth
5. Patients who are unable to understand the survey questions as designed (e.g., non-English speaking, etc.).
6. Patients who fail other study-specific screening questions.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
HealthCore, Inc.
INDUSTRY
Member Companies of the Opioid PMR Consortium
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Soledad Cepeda, MD, PhD
Role: STUDY_CHAIR
Janssen Research & Development, LLC
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
3033-9
Identifier Type: OTHER
Identifier Source: secondary_id
Observational Study 3033-9
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.