跳至主要内容
临床试验/ISRCTN13802038
ISRCTN13802038进行中(未招募)Unknown

Cluster randomized controlled feasibility study of CONNECT: a patient decision aid designed to improve the quality of shared decision-making for planned coronary angioplasty.

The Open University0 个研究点目标入组 340 人开始时间: 2023年9月25日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
入组人数
340

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. CLUSTERS/CARDIOLOGY DEPARTMENTS
  • Any NHS centre in England providing care for patients treated with planned (i.e. non-urgent) coronary angiogram query proceed, or coronary angioplasty, will be eligible to participate. The inclusion criteria for Cardiology Departments are:
  • 1.1. NHS Trust is in England
  • 1.2. Pre-assessment clinics embedded in the patient pathway.
  • 1.3. Has the capacity to recruit 40 patient participants within 12 months.
  • 1.4. Willing to be randomised to the intervention or control arm and adhere to arm allocation.
  • 1.5. Cardiology teams are willing to participate in a 2-3-hour training session about the intervention CONNECT.
  • 2. PATIENT PARTICIPANTS
  • Patient participants scheduled for planned coronary angiogram query proceed, or coronary angioplasty will be eligible to participate. Eligible patient participants will be:
  • 2.1. Adult patients (>=18 years) presenting with stable angina.
  • 2.2. Suspected or diagnosed chronic coronary artery disease.
  • 2.3. On the waiting list for planned coronary angioplasty or angiogram ± coronary angioplasty.
  • 2.4. Capacity to give informed consent.
  • 3. HEALTH PROFESSIONAL PARTICIPANTS
  • Eligible NHS staff participants will be:
  • 3.1. Working, or have worked, in the cardiology department delivering care for people scheduled for coronary angioplasty or coronary angiogram ± coronary angioplasty.
  • 3.2. Have had direct involvement in the delivery of CONNECT and/or the feasibility study procedures.

排除标准

  • 1. Clusters/Cardiology Departments who do not fulfil the inclusion criteria will be excluded.
  • 2. Patient participants who are clinically unstable, scheduled for urgent or emergency coronary angioplasty, or lack capacity to give informed consent at the time of recruitment will be excluded.
  • 3. Health professionals not involved in the CONNECT study or 'angioplasty' patient care will be excluded.

研究者

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