استانداردسازی گزارش در مطالعات کارآزمایی بالینی: کانسورت
Authors
Abstract:
Background and Objective: Interventional clinical trial is the study in which the participants are simultaneously placed in the intervention and control groups to investigate the cause-effect relationship between an intervention and an outcome. Because of the probability of some bias in human intervention, non-standard clinical trials design produce unreal interventional results. For standardizing the clinical trials, Consolidated Standards of Reporting Trials (CONSORT) statement was presented that is a guideline including the design, implementation and reporting of the results. CONSORT statement includes a flowchart and a Flow Diagram. CONSORT statement has a 25-item list that describes how to write a title, abstract, introduction, methods, results, discussion, registration, and access study protocol and sources of research funding. In the Flow Diagram of CONSORT, the way to access the participants, along the study, is taken into consideration. Of the importance of clinical trials on new diagnostic and therapeutic methods, present study was conducted to survey and evaluate the performance of CONSORT statement. Key words: Clinical trial, Randomized Clinical Trial, Intervention, Consort Funding: This research was funded by Rafsanjan University of Medical Sciences. Conflict of interest: None declared. Ethical approval: The Ethics Committee of Rafsanjan University of Medical Sciences approved the study. How to cite this article: Ayoobi F, Rahmani MR, Assar S, Jalalpour S, Rezaeian M. The Consort (Consolidated Standards Of Reporting Trials). J Rafsanjan Univ Med Sci 2017; 15(10): 977-94. [Farsi]
similar resources
تصادفی سازی در مطالعات کارآزمایی بالینی: از تئوری تا عمل
Background & Aim: Randomized clinical trials (RCTs) are studies which are able to provide the most valid evidence to compare various interventions in health research. Biases can affect the quality of research and ultimately make the results of a study invalid. One of the most important biases is selection bias. The best way to reduce selection bias is the use of random allocation. The aim of th...
full textتصادفی سازی در مطالعات کارآزمایی بالینی: از تئوری تا عمل
زمینه و هدف: کارآزمایی های بالینی تصادفی شده از جمله مطالعاتی هستند که قادرند معتبرترین شواهد را برای مقایسه مداخله های گوناگون در پژوهش های بهداشتی و درمانی فراهم سازند. وجود انواع تورش می تواند بر کیفیت پژوهش تأثیر گذارد و در نهایت، نتایج یک مطالعه را نامعتبر سازد. یکی از مهم ترین تورش ها، تورش انتخاب است. بهترین روش جهت کاهش تورش انتخاب، استفاده از تخصیص تصادفی شرکت کنندگان به گروه های موردن...
full textبرآورد اثرات درمانی در مطالعات کارآزمایی بالینی متقاطع در حضور عدم تمکین بیماران
Background & Objectives: In clinical trials some of participants do not take assignment treatment. Intention-to-treat (ITT) is one of the strategies to analyze of clinical trials with control. ITT estimation will be invalid and incorrect to show of treatment effects in case of existing non-compliance in participants. In this study we adjusted noncompliance effect to compare of active treatment ...
full textتحلیل به قصد درمان در مطالعات کارآزمایی بالینی: یک مطالعه مروری
Background & Aim: Randomized controlled trials often suffer from two major problems, i.e., noncompliance and missing outcomes. One potential solution to this problem is using the intention-to-treat (ITT) analysis approach. Therefore, the aim of this study was to review the concept of ITT and the most important issues related to it in practice since RCT researchers utilize it as a guide in order...
full textMy Resources
Journal title
volume 15 issue 10
pages 977- 994
publication date 2017-01
By following a journal you will be notified via email when a new issue of this journal is published.
No Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023