Prevention of Benzodiazepine Misuse in Primary Care
Benzodiazepine Dependence, Benzodiazepine Abuse, Substance Use Disorders
About this trial
This is an interventional treatment trial for Benzodiazepine Dependence focused on measuring Primary Health Care, Benzodiazepines, Substance Use Disorder, Addiction, Prescription Drugs
Eligibility Criteria
Inclusion criteria for primary health care centers:
- Employs at least two full-time physicians
- Has at least 3000 patients
- Has a regional care agreement (contract)
Exclusion criteria for primary health care centers:
- In operation for less than 12 months
- Participated in an intervention to reduce benzodiazepine prescriptions in the last 12 months
Sites / Locations
- Region Stockholm, Academic primary health care center
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Educational intervention with prescription feedback
Information on guidelines
No active intervention: standard care
The manager and physicians at each intervention center will participate in a brief educational intervention about benzodiazepines and benzodiazepine-like hypnotics and receive 12 months of targeted feedback on prescription of these drugs. The education will cover national and regional treatment guidelines for anxiety, depression, and insomnia, which include guidelines on prescription of benzodiazepines and benzodiazepine-like hypnotics.
The manager and physicians at each center in the active control group will receive written information on national and regional treatment guidelines for anxiety, depression, and insomnia, which include guidelines on prescription of benzodiazepines and benzodiazepine-like hypnotics. These centers will not receive the onsite educational intervention or 12 months of targeted prescription feedback.
The manager and physicians at each primary health care center in the passive control group will receive no active intervention. The passive control group will consist of primary health care centers that are not actively participating in the study. Data will be gathered from regional registers and databases. Thus, there will be no need to contact or communicate directly with the centers. This arm will be used only if the General Data Protection Regulation continues to allow access to regional registers and databases in primary health care.