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.
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.
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