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临床试验/NCT07379073
NCT07379073尚未招募不适用

Evaluation of a Clinical Support Website for the Management of Common Mental Health Conditions in Primary Care on Compliance With Benzodiazepine Prescribing Recommendations

MSPU de Pins-Justaret0 个研究点目标入组 100 人开始时间: 2026年6月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
主要终点
Compliance with recommended maximum duration of benzodiazepine prescriptions among new users

研究概览

简要总结

This cluster-randomized study aims to evaluate the impact of a web-based clinical support tool on adherence to recommended maximum durations for benzodiazepine prescriptions among new users in primary care. General practitioners (GPs) participating in the study will have access to the website, which provides evidence-based algorithms for the management of common mental health conditions, including anxiety and sleep disorders. Prescription data and patient characteristics will be extracted from the French national health insurance database (DCIR). The primary outcome is the proportion of new benzodiazepine users whose prescriptions comply with recommended duration guidelines. Multilevel logistic regression models will assess the intervention effect, adjusting for patient- and GP-level factors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Being a general practitioner or a specialist in general medicine.
  • Practicing in the Occitanie region.
  • Working in private practice.
  • Being registered under Sector 1 fee agreements.
  • Providing informed consent to participate in the study.
  • Having computer equipment in the medical office, available during consultation (desktop, laptop, tablet, or smartphone) with internet access.

排除标准

  • - Physicians who have been practicing for less than two years, as they are unlikely to have sufficient retrospective data on prescription reimbursements for their patients.

研究组 & 干预措施

Experimental Group (trained on PsychoMG website)

Experimental

Training intervention on benzodiazepine prescribing with access to the PsychoMG website providing evidence-based clinical decision algorithms for anxiety and sleep disorder management.

干预措施: Training (Other)

Control Group

No Intervention

Training intervention on benzodiazepine prescribing without access to the PsychoMG website providing evidence-based clinical decision algorithms for anxiety and sleep disorder management.

结局指标

主要结局

Compliance with recommended maximum duration of benzodiazepine prescriptions among new users

时间窗: 12 months

Primary outcome measure: adherence to recommended prescription duration (yes/no) for benzodiazepines A patient is considered to have a prescription duration for benzodiazepines that is either adherent or non-adherent if they had no benzodiazepine exposure in the previous year and their duration of exposure during the first treatment episode: 1. is less than 12 weeks for anxiolytic benzodiazepines, 2. is less than 28 days for hypnotic benzodiazepines and related drugs, in accordance with current recommendations.

次要结局

未报告次要终点

研究者

发起方
MSPU de Pins-Justaret
申办方类型
Other
责任方
Sponsor

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