Optimizing Weblinks Used in Digital Vaccination Invitations to Raise Trust and Booking Intention: Online Experiment 2
2 other identifiers
interventional
1,203
1 country
1
Brief Summary
This study investigates how the design of web links in digital vaccination invitation emails affects recipient trust and their willingness to book an appointment. Researchers compare three different weblink formats: a control third-party link previously used by the NHS ("accurx"), and two experimental weblinks in which the original link is hidden: a shortened "bit.ly" link, and a text-embedded hyperlink. The study primarily tests whether the two experimental weblinks will be perceived as more trustworthy and increase booking intention compared to the control weblink. Furthermore, the study examines whether the experimental weblinks is perceived to be more fluent (easier to read) and improves participants' ability to correctly identify the organisation (e.g., the NHS or a US pharmacy) that sent the hypothetical email. To test these effects, investigators will gather data from 600 participants from the United Kingdom and 600 from the United States. They will be randomly assigned to view one of the three hypothetical email versions. UK participants will see emails appearing to be from the NHS, while US participants will see emails from a fictitious pharmacy (Pharma-US). This research aims to provide evidence on how to design more effective and trustworthy digital health communications.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 13, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 23, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 23, 2022
CompletedFirst Submitted
Initial submission to the registry
March 24, 2026
CompletedFirst Posted
Study publicly available on registry
April 16, 2026
CompletedApril 16, 2026
April 1, 2026
10 days
March 24, 2026
April 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Perceived Trustworthiness
Participants rated the perceived trustworthiness of the vaccination invitation email on a 5-point Likert scale, where 1 represents "Very suspicious", and 5 represents "Very trustworthy".
Immediately after the intervention
Booking Intention
Participants rated their likelihood of booking a vaccine appointment based on the email invitation using a 5-point Likert scale ranging from 1 ("Very unlikely") to 5 ("Very likely").
Immediately after the intervention
Secondary Outcomes (2)
Ease of reading
Immediately after the intervention
Host Identification
Immediately after the intervention
Study Arms (3)
Control
NO INTERVENTIONParticipants were assigned to view a hypothetical vaccination invitation email containing the control weblink (UK participants: accurx.thirdparty.nhs.uk/r/aafwaczmd5; US participants: accurx.thirdparty.pharmaus.com/r/aafwaczmd5)
Shortened URL
EXPERIMENTALParticipants assigned to this arm are shown a hypothetical COVID-19 booster vaccination invitation email featuring a shortened URL using a bit.ly domain. To ensure local relevance, the email stimulus is tailored to the participant's geographic location: UK participants view an email appearing to be from the NHS, while US participants view an invitation appearing to be from a fictitious pharmacy, Pharma-US.
Text-embedded link
EXPERIMENTALParticipants assigned to this arm are shown a hypothetical COVID-19 booster vaccination invitation email where the booking link was presented as a descriptive hyperlink (e.g., "Book your vaccine here") rather than a visible URL. Following the study's geographic customisation, UK participants viewed an email stimulus that appeared to be from the NHS, while US participants viewed an invitation that appeared to be from Pharma-US.
Interventions
The intervention involved presenting a hypothetical invitation to a COVID-19 booster vaccination via email. Participants were randomly allocated to view one of three versions of the invitation to evaluate how the specific design of the embedded weblink influences recipient trust and booking behaviour. To ensure local relevance, the email stimulus was adapted based on the participant's country of residence: participants in the United Kingdom saw invitations that appeared to be from the NHS, while those in the United States saw invitations that appeared to be from a fictitious pharmacy, Pharma-US. Following the intervention, participants evaluated the email's trustworthiness, the link's fluency, and their own intention to book a vaccine appointment.
Eligibility Criteria
You may qualify if:
- Residency: Must be a resident of either the United Kingdom or the United States
You may not qualify if:
- Attention Failure: Participants who failed the designated attention check included within the survey will be excluded from the analysis.
- Speeding: Participants who completed the study "too fast"- indicating a lack of meaningful engagement with the experimental stimuli - were filtered out
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Essexlead
- University of Southern Californiacollaborator
- Department of Health and Social Care, UKcollaborator
- Kingston Universitycollaborator
Study Sites (1)
University of Essex
Colchester, Essex, CO4 3SQ, United Kingdom
Related Links
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- This is a double-blind study in which participants were unaware of the specific experimental condition to which they had been assigned. Participants were randomly allocated to view only one of three possible versions of a hypothetical vaccination invitation email-featuring either a control link, a shortened URL, or a text-embedded hyperlink-and were not informed of the existence or nature of the alternative stimuli. This masking ensures that their evaluations of trustworthiness, fluency, and booking intentions were not influenced by a direct comparison between the different link designs. As the study was conducted as an online survey via a fully automated platform, there was no direct interaction between the investigators and the participants during the intervention. As the study was conducted as an online survey via a fully automated platform, there is no direct interaction between the investigators and the participants during the intervention.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Psychology
Study Record Dates
First Submitted
March 24, 2026
First Posted
April 16, 2026
Study Start
January 13, 2022
Primary Completion
January 23, 2022
Study Completion
January 23, 2022
Last Updated
April 16, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- The data and the study protocol were shared while the main scientific output was under review for publication. After acceptance for publication, all content will be made publicly available.
- Access Criteria
- The data and study protocol will be freely accessible to the public after the main scientific output is accepted for publication.
Anonymised study data is shared on the Open Science Framework