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临床试验/NCT06530472
NCT06530472Enrolling By Invitation不适用

The Relationship Between Belief, Expectation, and Adherence to Therapy During COVID-19 Pandemic: a Multigroup Cohort Study in Patients With Ischemic Heart Disease

Fondazione Don Carlo Gnocchi Onlus1 个研究点 分布在 1 个国家目标入组 196 人开始时间: 2021年5月18日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
196
试验地点
1
主要终点
NACE

研究概览

简要总结

The goal of this [type of study: observational study or clinical trial ] is to learn about, test, compare etc.] in [ describe participant population/health conditions ]. The main question [ it aims to answer are:

  • [question
  • [question Participants will [describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items ].

If there is a comparison group: Researchers will compare insert groups ] to see if insert effects

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • all patients diagnosed with ischaemic heart disease established by angiography;
  • reaching the age of majority;
  • score >= 26 on the Montreal Cognitive Assessment (MoCA) test (Nasreddine et al., 2005).

排除标准

  • presence of comorbidity with other pathologies in an active or advanced phase; -patients with a prognosis to be defined;
  • pregnancy;
  • participants with neurological pathologies that significantly impair their cognitive functions (e.g. advanced Parkinson's disease; Alzheimer's dementia...cardiac arrest with hypoxic damage);
  • participants with cognitive impairments that compromise comprehension and sharing of the contents of the questions, detected through the administration of the Montreal Cognitive Assessment (MoCA) test (Nasreddine et al., 2005).

结局指标

主要结局

NACE

时间窗: At baseline, 3, 6 and 12 months from the recruitment

Net adverse clinical event or NACE, defined as a composite of all-cause mortality, myocardial infarction, stroke or major haemorrhage. In this case, bleeding is definitive according to the BARC (Bleeding Academic Research Consortium) scale (Mehran et al., 2011).

Adherence

时间窗: At baseline, 3, 6 and 12 months from the recruitment

Measured by the percentage of days covered (Percentage of Days Covered, PDC) by antiplatelet therapy, beta-blockers, statins, ACE-I/Sartan, hypoglycaemic drugs, psychotropic drugs (anxiolytics; antidepressants). The PDC is defined as the proportion of days for which a patient has a supply of medication available. When multiple prescriptions are for the same day, reference is made to the maximum duration, and for overlapping prescriptions, sequential use of the two prescriptions is assumed by summing the days of supply for each. Any interruptions in therapy are also taken into account. Non-adherence is defined as a PDC of less than 80%, while non-persistence is defined as a gap in prescriptions of (Direct Oral Anticoagulants or Direct Oral Anticoagulants) DOACs ≥14 days (Yu et al., 2020).

MARS-i

时间窗: At baseline, 3, 6 and 12 months from the recruitment

Measure with theMARS-5-i questionnaire consists of five questions on forgetting, changing dosage, stopping, skipping, and taking less medication . The score ranges from 5 to 25, where a higher MARS-5-i score indicates higher self-reported adherence. One item assesses unintentional non-adherence and four items assess intentional non-adherence

次要结局

  • Extra visits(At baseline, 3, 6 and 12 months from the recruitment)
  • CAS(At baseline, 3, 6 and 12 months from the recruitment)
  • Anxiety(At baseline, 3, 6 and 12 months from the recruitment)
  • ICQ(At baseline, 3, 6 and 12 months from the recruitment)
  • Adherence to pharmacotherapy(At baseline, 3, 6 and 12 months from the recruitment)
  • CSS(At baseline, 3, 6 and 12 months from the recruitment)
  • BIPQ(At baseline, 3, 6 and 12 months from the recruitment)
  • Clinical data(At baseline, 3, 6 and 12 months from the recruitment)
  • Depression(At baseline, 3, 6 and 12 months from the recruitment)
  • Illness Expectations(At baseline, 3, 6 and 12 months from the recruitment)
  • Socio-demographic data(At baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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