NCT01341093已完成不适用
Educational Program With Telephone Follow-up for Patients After Percutaneous Coronary Intervention: Randomized Controlled Trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- change from baseline in perceived health status at six months
研究概览
简要总结
The purpose of this study is to elaborate an educative program that includes telephone follow-up and assess its impact on the perceived health status of patients submitted to percutaneous coronary intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult patients (18 years or more) of both sexes
- •Being submitted to the first coronary artery bypass graft surgery between April 2011 and July 2012
- •Having a properly functioning residential phone line
排除标准
- •No cognitive condition to participate (assessed through the Mini-Mental State Examination - MMSE)
- •Illiterate participants who did not reach the minimum score 13 on the MMSE
- •Participants with one to seven years of education who did not reach the minimum score 18 on the MMSE
- •Participants with eight or more years of education who did not reach the minimum of 26 points on the MMSE
结局指标
主要结局
change from baseline in perceived health status at six months
时间窗: baseline and six months
The questionnaire "Medical Outcomes Survey 36 - Item Short-Form" developed by Ware and Sherboune (1992) will be used to collect the data at baseline and at six months.
次要结局
- change from baseline in self-efficacy at six months(baseline and six months)
- change from baseline in anxiety and depression at six months(baseline and six months)
- change from baseline in treatment adherence at six months(baseline and six months)
研究者
Rejane Kiyomi Furuya
Ph.D
University of Sao Paulo
研究点 (2)
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