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临床试验/NCT06142838
NCT06142838招募中不适用

Community Pharmacist Intervention to Enhance Adherence in Cardiovascular Drug Initiators

University Ghent1 个研究点 分布在 1 个国家目标入组 1,600 人开始时间: 2023年10月3日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,600
试验地点
1
主要终点
NIH Patient Reported Outcomes Measurement Information System (PROMIS) Medication Adherence Scale (PMAS)

研究概览

简要总结

The goal of this clinical trial is to evaluate a community pharmacist intervention aimed at improving medication adherence in patients starting newly prescribed medication for cardiovascular disease prevention. The main questions it aims to answer are:

  • Does this community pharmacist intervention improve medication adherence?
  • Which patients benefit the most from the intervention?
  • How do patients experience the start-up of newly prescribed medication (which questions do they have and do they experience side effects?)?
  • How do patients and pharmacists experience the intervention?

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients presenting with a first prescription for one of the following drug classes: antihypertensive drugs (= low-ceiling diuretics, beta blocking agents (excl. non-selective beta-blocking agents), ACE inhibitors, angiotensin II receptor blockers, calcium channel blockers), lipid-lowering drugs (= statins), antidiabetic drugs (= metformin, glucagon-like peptide-1 (GLP-1) analogues, sodium-glucose co-transporter 2 (SGLT2) inhibitors), or any combination thereof.
  • Age 18 years or older
  • Community-dwelling

排除标准

  • The drug is prescribed for a non-cardiovascular indication (e.g. beta-blocking agent for migraine prophylaxis)
  • Communication with the patient is not possible (e.g. due to cognitive impairment, insufficient knowledge of Dutch or French language)

结局指标

主要结局

NIH Patient Reported Outcomes Measurement Information System (PROMIS) Medication Adherence Scale (PMAS)

时间窗: At 6 weeks and at 12 weeks follow-up

Patient-reported measure of medication adherence

次要结局

  • Healthcare utilization(Over 12 weeks post-baseline)
  • Medication Possession Ratio (MPR)(Over 26 weeks post-baseline)
  • Medication knowledge questionnaire(At 6 weeks and at 12 weeks follow-up)
  • Treatment response(At baseline and at 12 weeks follow-up)
  • Discontinuation rate(Over 26 weeks post-baseline)
  • Beliefs about Medicines Questionnaire (BMQ-Specific)(At 6 weeks and at 12 weeks follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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