Optimizing Weblinks Used in Digital Vaccination Invitations to Raise Trust and Booking Intention: Online Experiment 2

April 8, 2026 updated by: Marie Juanchich, University of Essex

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.

Study Overview

Status

Completed

Conditions

Detailed Description

This randomised experimental study investigates how weblink design influences the perceived trustworthiness of digital health communications. As digital invitations (e.g., emails and SMS) have become standard for public health initiatives such as vaccination programs, the use of third-party or disfluent (hard-to-read) web links may inadvertently undermine trust.

Study Protocol and Intervention

Participants will be randomly allocated to one of three experimental conditions. In all conditions, participants will read a hypothetical email invitation for a COVID-19 booster vaccine. The content of the emails remains identical except for the format of the booking weblink included in the email:

Control Condition: Features the "accurx" web link (accurx.thirdparty.nhs.uk/r/aafwaczmd5) based on a third-party format used in official invitations from the UK's NHS.

Experimental Condition 1: (Concealed in shortened URL) features a shortened version of the link using a bit.ly domain.

Experimental Condition 2: (Concealed, text-embedded) shows the link presented as a descriptive hyperlink.

To ensure relevance to the target populations, participants will see a version of the hypothetical email tailored to their country of residence: UK participants will see invitations sent from the NHS, while US participants will see invitations from a fictitious pharmacy (Pharma-US). Unlike the UK, COVID-19 vaccination in the US was predominantly organised by local pharmacies.

Primary Hypotheses

The study was designed to test six primary hypotheses:

  1. The email containing the two experimental weblinks will be rated as significantly more trustworthy than the control "accurx" weblink.
  2. Participants will report being more likely to use the link to book a vaccine appointment based on the experimental weblinks than the control "accurx" web link.
  3. Participants will find the two experimental weblinks more fluent (easier to read) than the "accurx" control link.
  4. Participants would be more likely to correctly identify the organisation that hosts the link based on the two experimental weblinks than based on the "accurx" control web link.
  5. Trustworthiness, booking intention, host identification accuracy, and fluency would be positively correlated with each other.
  6. The effect of the link will be mediated by the identification of the host organisation and the fluency of the link.

Measurement

Following the presentation of the hypothetical email, participants will rate the email on three 5-point Likert scales: trustworthiness (1: Very suspicious to 5: Very trustworthy), fluency (1: Very difficult to 5: Very easy), and booking intention (1: Very unlikely to 5: Very likely). Host identification will be assessed via a multiple-choice question with four options: the NHS, Pharma-US, Accurx, or 'Not sure'.

The investigators will aim to gather data from 600 participants from the UK and 600 from the US. They will be invited to complete the study via an online platform. Participants who complete the study too fast or failed the attention check will be excluded.

This study will be conducted as part of a larger research project exploring the broader relationship between the trustworthiness of digital messages and national vaccination rates.

The study hypotheses, design, measures and analyses were preregistered before the start of data collection on a different platform (AsPredicted). This time stamped preregistration protocol is linked as a document in this registration.

Study Type

Interventional

Enrollment (Actual)

1203

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Essex
      • Colchester, Essex, United Kingdom, CO4 3SQ
        • University of Essex

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Residency: Must be a resident of either the United Kingdom or the United States

Exclusion Criteria:

  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Participants 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)
Experimental: Shortened URL
Participants 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.

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.

Experimental: Text-embedded link
Participants 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.

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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Trustworthiness
Time Frame: Immediately after the intervention
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
Time Frame: Immediately after the intervention
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 Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ease of reading
Time Frame: Immediately after the intervention
Participants assessed the reading ease (or fluency) of the embedded weblink on a 5-point Likert scale, where 1 is "Very difficult", and 5 is "Very easy".
Immediately after the intervention
Host Identification
Time Frame: Immediately after the intervention
Participants were asked to identify the organisation that sent the communication by selecting one answer from a multiple-choice list of four options: the NHS, Pharma-US, Accurx, or Unclear/I don't know.
Immediately after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 13, 2022

Primary Completion (Actual)

January 23, 2022

Study Completion (Actual)

January 23, 2022

Study Registration Dates

First Submitted

March 24, 2026

First Submitted That Met QC Criteria

April 8, 2026

First Posted (Actual)

April 16, 2026

Study Record Updates

Last Update Posted (Actual)

April 16, 2026

Last Update Submitted That Met QC Criteria

April 8, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ETH 2122-0265 Expe2
  • CRUSA210009 (Other Grant/Funding Number: British Academy COVID-19 Recovery grant)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymised study data is shared on the Open Science Framework

IPD Sharing 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.

IPD Sharing Access Criteria

The data and study protocol will be freely accessible to the public after the main scientific output is accepted for publication.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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