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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02918656
Other study ID # IP-2014-09-7672
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date October 2016

Study information

Verified date June 2019
Source University Hospital of Split
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the investigators study is to evaluate the efficacy of infographics in presenting information, in terms of understanding and remembering research results, compared to standard PLS formats and scientific summary formats (SciSum).


Description:

The investigators will conduct a randomized control trial (RCT) with three different formats of the same systematic review summary (infographics, PLS and scientific summary). The content of these three formats is based on the same systematic review, but the ways of data presentation will differ: visual presentation, plain language, and scientific language. The trial will be performed at the beginning of the 2016/2017 academic year, with first year university students as participants. The trial will be voluntary and anonymous. The survey will consist of 4 parts: 1) demographic data, 2) one format of the summary (randomly assigned), 3) comprehension test of the information given in the summary, 4) accessibility of information and overall satisfaction with the given summary assessed by survey and 5) health numeracy test. All materials will be in Croatian. The materials used in this research will be assessed by experts in order to confirm face validity of developed questions.


Recruitment information / eligibility

Status Completed
Enrollment 171
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Eligible participants will be first-year university students without experience with Cochrane review summaries, because prior familiarization with Cochrane summaries could make information uptake easier by those participants.

Exclusion criteria:

- Participants who give the positive answer to the survey question about familiarity with the Cochrane will be excluded from the study analysis.

Study Design


Related Conditions & MeSH terms

  • Understanding Cochrane Systematic Reviews

Intervention

Other:
Infographic presentation of health information
The students in this group will read Cochrane systematic review summary in infographics format. Infographics format is a form of visual presentation of results of systematic review, supported by pictures and graphs.
PLS presentation of health information
The students randomized in PLS group will read text format with simple explanation of the survey topic main findings which is intended for lay audience.
Scientific abstract presentation of health information
The students in scientific abstract group will read the the text written for the academic population and practitioners.

Locations

Country Name City State
Croatia School of Medicine Split

Sponsors (2)

Lead Sponsor Collaborator
University Hospital of Split Croatian Science Foundation

Country where clinical trial is conducted

Croatia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Understanding The primary outcome of the study is the score on a understanding test with ten questions about information contained in all three forms of presentation, titled as "Understanding information about external cephalic version for breech presentation before term" (Hutton et al, 2015). The questions will focus on understanding the benefits and risks of the intervention and the quality of evidence described in the systematic review. Each correctly answered question will be awarded one point, with a maximum of 10 points. The scale was specifically designed for this research, they ask about the information contained in all three abstract format and all questions are open-ended. One-hour after the intervention
Secondary Reading Experience This section of the survey will include 5 questions about the experience of participants about the text they read, measured on a 10-point Likert type scale, where 1 means do not agree at all and 10 means fully agree. The total score is the sum of scores on all five answers (minimum score was 10 and maximum 50). Higher scores indicate greater reading experience, which means that a person was assessed that type of reading material as more enjoyable. So, higher scores are associated with more positive reading experience. One hour after the intervention
Secondary Accessibility of Relevant Information This section of the survey will have 5 questions concerning how easy it was for the participant to find relevant information, measured by a 10-point Likert type scale where the answer 1 means I do not agree at all and 10 means I fully agree. The total score is the sum of scores on all the answers (minimum score was 5, maximum 50). The higher score indicated that the reading material was perceived as more user friendly and that it was easier to find the desired information. One hour after the intervention
Secondary Health Numeracy Score This section will use 6-item General health numeracy test (Osborne et al., 2013) in order to determine how much our participants understand the basic health instructions regarding numeracy dimension. For each correct answer, the participants receive one point and the total score is the sum of all correct answers. One hour after the intervention