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临床试验/NCT03020316
NCT03020316已完成不适用

Peer Mentored Approaches For Men And Women With Coronary Artery Disease ("4Steps")

Weill Medical College of Cornell University2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2016年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
2
主要终点
Perceived Stress

研究概览

简要总结

This study will be a pilot prospective randomized study using a peer mentor with or without Transcendental Meditation as compared to usual care for men and women with a new diagnosis of coronary artery disease (CAD). The study is designed to explore between cohort comparisons of perceived stress and a number of additional outcomes. The results of this pilot study will be used in the design of larger future trials.

The target population is adult men and women with a new diagnosis of CAD made on the basis of a myocardial infarction, coronary revascularization procedure, acute coronary syndrome, or imaging test suggestive of CAD.

The overall hypothesis of this proposal is that the addition of a peer mentor and training in Transcendental Meditation to usual care will improve perceived stress and medication adherence for men and women with newly diagnosed CAD as compared with usual care.

详细描述

The overall hypothesis of this proposal is that the addition of a peer mentor and training in Transcendental Meditation to usual care will improve perceived stress and medication adherence for men and women with newly diagnosed CAD as compared with usual care.

Participants will be "randomized" into one of two study groups:

Arm 1 - Standard Of Care (SOC) Arm 3 - SOC, assignment of a peer mentor, and the opportunity to receive training in transcendental meditation

We are no longer enrolling in Arm 2 of the study (SOC and subjects addition of a peer mentor).

Subjects will be assessed at baseline, 1 month, 6 months, and 12 months with surveys and assessments.

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
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For Participants:
  • Men and women aged 18-90
  • English speaking
  • Newly diagnosed with CAD (myocardial infarction [MI], percutaneous coronary intervention [PCI], coronary artery bypass graft [CABG]), acute coronary syndrome, or any imaging test suggestive of CAD).
  • For Mentors:
  • (Male mentors will be paired with male participants, and female mentors will be paired with female participants.)
  • Men and women aged 18-90
  • English speaking
  • Established (greater than 1yr prior to study) diagnosis of CAD (myocardial infarction [MI], percutaneous coronary intervention [PCI], coronary artery bypass graft [CABG] acute coronary syndrome, or imaging test suggestive of CAD).

排除标准

  • For Participants:
  • Previously diagnosed CAD (MI, PCI, CABG, acute coronary syndrome or imaging test suggestive of CAD)
  • Inability or unwillingness to provide written consent
  • Non-English speaking
  • Prior formal training and practice of TM
  • For Mentors:
  • Inability or unwillingness to provide written consent
  • Non-English speaking

结局指标

主要结局

Perceived Stress

时间窗: 52 weeks

Cohen Perceived Stress Scale (PSS-10) Each item is rated on a 5-point scale ranging from never (0) to almost always (4). Positively worded items are reverse scored, and the ratings are summed, with higher scores indicating more perceived stress. Total scale range: 0-40. Scores around 13 are considered average. Scores of 20 or higher are considered high stress.

次要结局

  • Medication Adherence (ARMS-7)(52 weeks)
  • Medication Adherence (VAS)(52 weeks)
  • Depressive Symptoms(52 weeks)
  • Heart rate(52 weeks)
  • Waist circumference(52 weeks)
  • Lipid panel results(52 weeks)
  • Fasting plasma glucose(52 weeks)
  • Hospital readmission(52 weeks)
  • Changes in physical activity(52 weeks)
  • Number and manner of contacts between participants and mentors(52 weeks)
  • Participant feedback about mentorship and TM(52 weeks)
  • Participant knowledge about CAD(52 weeks)
  • Height(52 weeks)
  • Weight(52 weeks)
  • Blood pressure(52 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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