Randomised Study Within a Review (SWAR) to Compare Communication of the Findings of Systematic Reviews to the Public by Plain Language Summary or Video Abstract
NCT ID: NCT07333924
Last Updated: 2026-01-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
PHASE3
100 participants
INTERVENTIONAL
2026-01-15
2026-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Studies Within A Review (SWARs) are studies which are embedded into a systematic review and aim to form an evidence base to improve how we plan, do, and share systematic reviews. SWARs offer a promising way of improving the methodology of systematic reviews and dissemination of their findings.
This randomised trial aims to address the current research gap by identifying the effectiveness of two different ways to communicate systematic review findings to the public and determining which methods are more suitable for different audiences: participants will be asked to read a summary or watch an animated video of a summary of both reviews and then complete a questionnaire about the reviews' findings and conclusions. The study will assess outcomes such as comprehension, perceived understanding, engagement, and interest of participants in reading the full reviews.
By evaluating the impact of different communication strategies, this study aims to strengthen the evidence base for methods to communicate complex scientific findings to the public. The results are expected to provide valuable insights for optimising the communication of the key findings of systematic reviews, ensuring that summaries are clear, engaging and accessible.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Communicating Evidence From Systematic Reviews to the Public
NCT01939925
Evaluating the Impact of Assessing During Peer Review the CONSORT Checklist Submitted by Authors
NCT03751878
Presenting Summary Information From Cochrane Systematic Reviews: Protocol for Research of Infographics Presentation vs. Plain Language Summary
NCT02980107
Comparison of Different Frames of Numerical Information in Cochrane Plain Language Summaries
NCT03554252
Presenting Summary Information From Cochrane Systematic Reviews to Physicians
NCT03002610
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Systematic Review 1: Clinical Utility of Biomarkers for Outcomes Prediction in Adults with Suspected Sepsis Presenting to the Emergency Department Sepsis is associated with a high mortality rate, and early detection and diagnosis is crucial. This review aimed to determine whether biomarkers measured in patients presenting to an emergency department with suspected sepsis may predict deterioration, including mortality, critical care admission, organ failure, and septic shock.
Systematic Review 2: Local antibiotics for patients undergoing surgery for open fractures Open fractures are serious injuries where the bone breaks through the skin, often leading to complications like infection. Treating these injuries can be complex and expensive, with many patients needing multiple operations and ongoing care. This review sought to determine if there is evidence that local antibiotics may reduce infection in people who are having surgery for open fractures.
The objectives of this study are
1. To determine whether a plain language summary or animated video summary is more effective in conveying the core message of a systematic review.
2. To compare the effects of the two methods on perceived understanding, engagement, and interest in reading the full text of the systematic review
Recruitment plan We will recruit using multiple methods. The study will be advertised through various channels, including posters displayed in common areas of the host university (Queen's University Belfast) and other popular locations across Belfast, social media platforms such as Instagram, Twitter and LinkedIN, and word of mouth. People interested in taking part will be able to contact the research team directly using the provided contact details.
Study procedures Potential participants will email or click on a QR code on the study posters (in person or via social media), which will bring them to the study information and a consent form. They will read that their participation will take a maximum of 30 minutes for the first round, and that they will asked to participate in a second round of questions 1 to 2 weeks later, which can be done via telephone pr email if preferred and would take less than 10 minutes. They will be asked to include their first name or a nick-name and contact details (email or telephone) so that the research team can contact them. Participants will also be asked to answer some additional questions to collect their age, scientific education and whether they had any scientific training after secondary education, and if they feel they know anything about the review topics.
The research team will contact those who have volunteered and have agreed to participate by email or telephone. A meeting will be arranged for a public space where they can sit comfortably with minimal noise and distractions. Participants will be randomly assigned to one of two groups: either the Reading Group or the Video Group (as shown in Table 1). Within each group, participants will be randomly assigned to start with Review 1 or Review 2. Once people are enrolled in the study, they will be assigned a unique ID number.
The intervention will be administered on a tablet computer. Those in the Reading Group will read the summary of their first review on the tablet and then answer related questions. After completing this review, they will read the summary of their second review and answer corresponding questions. Participants in the Video Group will use headphones while watching the Animated Video summary of their first review and then answer related questions on the tablet. After completing that review, they will watch an Animated Video summary of their second review and answer corresponding questions.
Participants will be reminded that they will be contacted for a follow-up assessment 1-2 weeks after the initial session. They will be contacted using the contact method they provided during the consent process. Follow-up can be face-to-face, or by email or phone.
Statistical analysis Participants' responses related to the Plain Language Summary and Animated Video Summary of Review 1 and Review 2 will be compared. Differences between groups will be assessed using the T-test/Mann-Whitney U test (as appropriate). A convenience sample of 100 participants will be sought, based on the time available for the researcher to conduct the data gathering.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Reading group
Written summary of a systematic review
Plain language summary
A written summary of the systematic review.
Video group
Video summary of a systematic review
Animated video
An animated video summary of the systematic review.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Plain language summary
A written summary of the systematic review.
Animated video
An animated video summary of the systematic review.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Any gender
* Able to read and understand English
* Willing to read and listen to review summaries, and answer questions
* Provide informed consent to participate
Exclusion Criteria
* People who do not read or understand English
* People with hearing or visual impairment
* People under 18 years of age
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aberdeen Belfast Evidence Collaboration
UNKNOWN
Queen's University, Belfast
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mike Clarke
Chair, Research Methodology
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
Maguire LK, Clarke M. How much do you need: a randomised experiment of whether readers can understand the key messages from summaries of Cochrane Reviews without reading the full review. J R Soc Med. 2014 Nov;107(11):444-9. doi: 10.1177/0141076814546710. Epub 2014 Oct 23.
Devane D, Burke NN, Treweek S, Clarke M, Thomas J, Booth A, Tricco AC, Saif-Ur-Rahman KM. Study within a review (SWAR). J Evid Based Med. 2022 Dec;15(4):328-332. doi: 10.1111/jebm.12505. Epub 2022 Dec 13. No abstract available.
Related Links
Access external resources that provide additional context or updates about the study.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SWAR02-2026
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.