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临床试验/NCT06525805
NCT06525805已完成不适用

Readers' Attention of Shorter Versus Longer Abstracts of Systematic Reviews: A Randomized Controlled Trial

University of Oldenburg1 个研究点 分布在 1 个国家目标入组 1,941 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,941
试验地点
1
主要终点
Trial participation

研究概览

简要总结

The present randomized controlled trial (RCT) was designed to investigate the perceptions of researchers on systematic review (SR) abstracts. The primary objective will be to compare readers' attention of shorter versus longer abstracts. The secondary objective will be to assess the perception of an abstract based on four indicators of a well-written abstract: (a) Informativeness, (b) Accuracy, (c) Attractiveness, and (d) Conciseness.

The study will involve researchers from all over the world who recently published an SR, regardless of their research field. To identify eligible authors, a search of MEDLINE (via PubMed) was conducted on May 5, 2024, for systematic reviews published between January 1, 2024, and March 26, 2024. A total of at least 6200 SRs will be selected from PubMed and assessed for eligibility. The corresponding author information will be extracted from all included SRs and randomized in a 1:1 ratio.

详细描述

This study will attempt to emulate the reading process observed in PubMed. When searching PubMed, researchers are initially presented with an overview of the references identified. After clicking on the title, the corresponding abstract appears. For full-text access, researchers must actively follow a separate link to the journal page.

In this RCT, participants will be randomly assigned in a 1:1 ratio to two groups (those receiving a long abstract vs. those receiving a short abstract). Both groups receive the same cover letter by e-mail explaining the purpose of the study, the use of the data, measures to ensure anonymity of participation, and a link for participation.

The link will direct participants to SoSci Survey, an online survey tool. Those in the group receiving the long abstract will see an abstract with a length of 771 words (PMID: 37955353). Those in the group receiving the short abstract will see an abstract with a length of 277 words (PMID: 37942649). Both abstracts are structured and pertain to the same review entitled "Percutaneous nephrolithotomy vs. retrograde intrarenal surgery for renal stones". This review was published once in the Cochrane Database of Systematic Reviews and once in the journal BJU International.

The design of the abstract presented is similar to that of PubMed, but no title or authors will be indicated. After reading the abstract, participants must actively click the "Continue" button to proceed with the survey.

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 (Participant)

盲法说明

The participants will be blinded to the intervention. In the cover letter, participants will be informed that the study aims to examine the characteristics of an abstract. However, they will not be informed that the primary focus of this study is the influence of the abstract´s length. Furthermore, the participants will be not aware of the number of different abstracts that were randomly allocated.

入排标准

性别
All
接受健康志愿者

入选标准

  • The corresponding authors of systematic reviews that were indexed in PubMed between January 1, 2024, and March 26, 2024, and for which an English abstract is available will be included. These include authors of all types of SR, with the majority likely representing SRs on effectiveness. Authors of other types of evidence syntheses (e.g. scoping reviews, methodological papers), editorials, protocols, corrections, retractions, erratums, or summaries of SRs will be excluded.
  • For identifying the systematic reviews from which the corresponding authors will be contacted we will use the following eligibility criteria.
  • Inclusion Criteria:
  • Systematic reviews of all types

排除标准

  • No English abstract
  • Other types of evidence syntheses (e.g. scoping reviews, methodological papers)
  • Protocols
  • Editorials
  • Others: e.g. Corrections, retractions, erratums, or summaries of SRs
  • No email address available

结局指标

主要结局

Trial participation

时间窗: Immediately after reading the abstract

The primary outcome of this RCT will be the trial participation, which is defined as the proportion of participants who read the abstract and then clicked on the "Continue" button. This will be quantified by dividing the number of participants who read the abstract and proceeded to complete the survey by the total number of individuals who clicked on the link in the email. Information will be electronically captured in SoSci survey.

次要结局

  • Indicators of a well-written abstract(Immediately after reading the abstract)

研究者

发起方
University of Oldenburg
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jasmin Helbach

Principal Investigator

University of Oldenburg

研究点 (1)

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