跳至主要内容
临床试验/NCT04877171
NCT04877171Unknown不适用

Telemedicine Efficacy in Medication Adherence in Post-ischemic Stroke Patients

Fundación Cardiovascular de Colombia1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2021年7月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
84
试验地点
1
主要终点
Percentage medication adherence through Morisky-Green questionnaire

研究概览

简要总结

Telemedicine is an incipient resource to support the stroke system of care in Colombia. Several studies had demonstrated that patients benefit by implementing telestroke, for instance, providing timely and appropriate neurological consultation, diminishing accessible barriers, improving medication adherence for secondary prevention and facilitating linkages between patient and physician, especially for those in rural or neurologically underserved areas.

Hypothesis: The use of Telemedicine improves medication adherence in Post-ischemic Stroke.

Study Design: This is a randomized, single-blind, clinical trial to assess the efficacy of Telemedicine, over medication adherence in Post-ischemic Stroke subjects from Colombia.

Population: Eighty-four Post-ischemic Stroke subjects, subjects of both genders, over 18 years old, with a first stroke will be included.

Ethical Aspects: The study will be conducted according to the Helsinki declaration, the good clinical practices guidelines and the Colombian legislation. Prior to entering the study, patients must sign a written or oral informed consent that has been approved by the Institutional Ethics Committee of Fundación Cardiovascular de Colombia.

Overall objective: this study aims to determine the efficacy of telemedicine on pharmacological adherence in post-ischemic Stroke Participants.

Focus of study: Adherence to secondary stroke prevention medication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 86 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •First ischemic stroke.
  • •Lived in urban areas.
  • •Available Access to permanent internet at home, in work on mobile dispositive, computers or tablets.
  • •Patients who gave their written informed consent.

排除标准

  • •Diagnosis of neurodegenerative diseases such as dementia and Parkinson's disease.
  • •Diagnosis of Diseases-terminal to prevent tracking.
  • •Diagnosis of psychiatric illnesses such as major depressive disorder (MDD) or others.
  • •Global cognitive impairment or previous diagnosis of dementia.

研究组 & 干预措施

telemedicine neurology consultation

Experimental

Starting on day 12-14 post-discharge, participants will receive a phone call for a drug conciliation. Participants at 1-month post-discharge will receive a telemedicine consultation, another at 3 months and 6 months.

干预措施: telemedicine neurology consultation (Other)

in-person neurology consultation

Active Comparator

Starting at 1-month post-discharge, participants will attend an in-person neurology consultation and the following consultations depend on their physician's criteria until completed 6 months post-discharge.

干预措施: in-person neurology consultation (Other)

结局指标

主要结局

Percentage medication adherence through Morisky-Green questionnaire

时间窗: 6 months

The Morisky Medication Adherence Scale in the original version (MMAS-4) is a structured self-report measure of medication-taking behavior. It consists of 4 items, with binary scoring (yes/no). Patients score one point for every 'Yes' answer. A score of 0 indicates high adherence; a score of 1 or 2 indicates intermediate adherence, and a score of 3 or 4 indicates low adherence.

次要结局

  • The Fantastic lifestyle assessment questionnaire(6 months)
  • Caregiver burden questionnaire(6 months)

研究者

发起方
Fundación Cardiovascular de Colombia
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Telemedicine Efficacy in Medication Adherence in... | 临床试验