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Spots Global Cancer Trial Database for The Impact of Picture Narrative Format on Print Lung Screening Communication Outcomes

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Trial Identification

Brief Title: The Impact of Picture Narrative Format on Print Lung Screening Communication Outcomes

Official Title: The Impact of Picture Narrative Format on Knowledge and Acceptability for Lung Screening Print Decision Support Materials

Study ID: NCT05016570

Study Description

Brief Summary: The purpose of this study is to test whether a picture narrative format is more successful, than text with pictures or text alone, in communicating lung screening information (primarily defined by positive attitudes towards the design and increase in knowledge) to people likely to be invited to lung screening where available.

Detailed Description: Population screening is key to detecting lung cancer early at a more treatable stage. Uptake of screening should be equitable (i.e., screening benefits all eligible members of the population and does not contribute further to health disparities) and informed (i.e., participants have been involved in the decision to take part and their decision aligns with their values and circumstances). Print decision support materials are the primary mechanism for encouraging engagement with cancer screening and supporting decision making. It is essential that we identify print communication techniques that are effective in informing invitees about lung screening. The intervention, picture narrative information about lung screening, was previously developed through codesign and prototype testing with people likely to be eligible for lung screening (50 to 75 years old, past or current heavy smokers). Participants will be randomised to one of three groups: Picture narrative format, Text with pictures (control 1) or, Text-only (control 2). This study will assess whether presenting lung screening information in a picture narrative format can improve lung cancer screening knowledge, eligibility self-assessment and attitudes. It will also assess whether perceptions of the information designs can explain any impact of the intervention on these outcomes and whether there are differences across socioeconomic groups.

Eligibility

Minimum Age: 49 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Mental Health and Wellbeing, University of Glasgow, Glasgow, , United Kingdom

Contact Details

Name: Kathryn Robb, PhD

Affiliation: University of Glasgow

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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