NCT07675694

Brief Summary

Chest X-rays are commonly used to help diagnose and manage chest conditions. Artificial intelligence (AI) tools are increasingly being used to support chest X-ray interpretation. However, it is not yet clear whether the timing of AI information affects how clinicians review images, make decisions, and use AI support. This study will look at whether showing AI information before or after a clinician first reviews a chest X-ray changes how they look at the image, how long they take, their interpretation decisions, their confidence, and their trust in AI support. Healthcare professional participants will complete two chest X-ray interpretation sessions in a controlled NHS research setting. During each session, participants will review de-identified chest X-ray images while wearing eye-tracking equipment. Eye-tracking will record where a participant looks on the image and how long they spend looking at different areas. In one session, AI information will be shown before the participant reviews the chest X-ray. In the other session, AI information will be shown after the participant has first reviewed the chest X-ray. The order of these two sessions will be balanced across participants. The study uses de-identified chest X-ray images from existing examinations. It does not involve patients directly, does not change clinical care, and no clinical decisions will be made from the study readings. Participants will also complete a short questionnaire about their experience of using AI support. A separate anonymous survey will collect wider views from clinicians, patients, members of the public, and healthcare staff about the use of AI in chest X-ray interpretation.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
4mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress21%
Jun 2026Dec 2026

First Submitted

Initial submission to the registry

June 10, 2026

Completed
20 days until next milestone

First Posted

Study publicly available on registry

June 30, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

June 30, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

July 6, 2026

Status Verified

July 1, 2026

Enrollment Period

5 months

First QC Date

June 10, 2026

Last Update Submit

July 2, 2026

Conditions

Keywords

Artificial intelligence timingChest X-ray interpretationVisual search behaviourDiagnostic accuracyTrust in automationAutomation biasClinician confidenceDecision support systemsHuman-AI interaction

Outcome Measures

Primary Outcomes (4)

  • Change in Chest X-ray Case Interpretation Time

    Case interpretation time is the duration, in seconds, from initial case display to final structured report submission. Change in case interpretation time will be measured between Session 1 and Session 2, displaying either original chest X-ray first or AI output first.

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Change in Chest X-ray Case Diagnostic Accuracy

    Diagnostic accuracy will be assessed using structured report outcomes compared with clinician-verified chest X-ray ground truth. Each participant's final structured interpretation for each chest X-ray case will be compared with the verified study ground truth for that case. Change in diagnostic accuracy will be measured between Session 1 and Session 2, displaying either original chest X-ray first or AI output first.

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Change in Chest X-ray Case Visual Search Behaviour

    Visual search behaviour will be assessed using predefined eye-tracking metrics that capture gaze location and search behaviour during chest X-ray interpretation. Metrics include time to first fixation, hit time, dwell time within abnormal case areas of interest, fixation count, mean fixation duration, revisit count, and fixation dispersion. Change in visual search behaviour will be measured between Session 1 and Session 2, displaying either original chest X-ray first or AI output first.

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Trust in AI Support After Reader-Study Completion

    Trust in AI support will be assessed using structured questionnaire ratings after participants have completed both Session 1 and Session 2. This measure captures participants' overall perceived usefulness, reliance on AI support, and willingness to revise decisions after reviewing AI information.

    Immediately after Session 2, anticipated average 5 weeks after enrolment

Secondary Outcomes (5)

  • Change in Chest X-ray Case Clinical Management Recommendations

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Change in Chet X-ray Case Decision Confidence

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Overall Reflective Confidence After Reader-Study Completion

    Immediately after Session 2, anticipated average 5 weeks after enrolment

  • Participant Perceptions of AI Support After Reader-Study Completion

    Immediately after Session 2, anticipated average 5 weeks after enrolment

  • Broader Attitudes Toward AI in Chest X-ray Interpretation

    2 months

Other Outcomes (5)

  • Differences in Chest X-ray Case Diagnostic Accuracy, Visual Search Behaviour, and Trust in AI Support by Clinical Background and Experience

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Association Between Chest X-ray Case Visual Search Behaviour and Diagnostic Accuracy

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • Association Between Chest X-ray Case Visual Search Behaviour and Case Complexity

    Session 1 at enrolment and Session 2 at least 4 weeks later, anticipated average 5 weeks

  • +2 more other outcomes

Study Arms (2)

Original CXR First Sequence

EXPERIMENTAL

Participants complete the original chest X-ray first timing condition in Session 1, followed by the AI output first timing condition in Session 2. Sessions are separated by at least four weeks.

Behavioral: Original CXR First TimingBehavioral: AI Output First Timing

AI Output First Sequence

EXPERIMENTAL

Participants complete the AI output first timing condition in Session 1, followed by the original chest X-ray first timing condition in Session 2. Sessions are separated by at least four weeks.

Behavioral: Original CXR First TimingBehavioral: AI Output First Timing

Interventions

Participants first review the original chest X-ray without AI output and complete an initial structured interpretation response. AI output is then introduced, and participants may review or revise their response before submitting the final response for that case.

AI Output First SequenceOriginal CXR First Sequence

Participants first view AI output before reviewing the original chest X-ray. The original chest X-ray is then introduced, and participants complete or revise their structured interpretation response before submitting the final response for that case.

AI Output First SequenceOriginal CXR First Sequence

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Main reader study:
  • Healthcare professionals aged 18 years or over
  • Registered to practise in the UK
  • Employed by the NHS or another healthcare service operating in the UK
  • Current or recent, within the last 3 years, clinical experience involving chest X-ray interpretation, review, or use in clinical practice
  • Able to attend two onsite study sessions at University Hospitals of Leicester NHS Trust at mutually agreed times
  • Able and willing to provide written informed consent
  • Compatible with the eye-tracking equipment
  • Supplementary survey:
  • Adults aged 18 years or over
  • Live in the UK or have used the NHS or another UK healthcare service within the last 5 years
  • Able to provide informed electronic consent
  • Belong to one of the following respondent groups: healthcare professionals or healthcare staff, patients or carers, or members of the public
  • Healthcare professional respondents may include adults involved in requesting, interpreting, checking, or acting on chest X-ray findings in clinical practice

You may not qualify if:

  • Main reader study:
  • Inability to attend both onsite study sessions at University Hospitals of Leicester NHS Trust
  • Eye-tracking incompatibility, such as visual, neurological, or physical conditions preventing adequate gaze tracking or participant comfort
  • Direct involvement in selection, adjudication, or preparation of the chest X-rays used in the study
  • Conflicts of interest, including direct involvement in development of the AI system under evaluation
  • Prior participation in a closely related AI chest X-ray study where overlap in image sets or study procedures may compromise validity, assessed on a case-by-case basis
  • Supplementary survey:
  • Aged under 18 years
  • Does not live in the UK and has not used the NHS or another UK healthcare service within the last 5 years
  • Unable to provide informed electronic consent
  • Does not meet one of the eligible respondent groups for the survey

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospitals of Leicester NHS Trust

Leicester, Leicestershire, LE1 5WW, United Kingdom

RECRUITING

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
No masking is used. It is clear to participants and study staff whether the chest X-ray or the AI information is shown first during each session.
Purpose
DIAGNOSTIC
Intervention Model
CROSSOVER
Model Details: Participants are randomly assigned to one of two session orders. In one order, participants review the chest X-ray first in Session 1 and the AI information first in Session 2. In the other order, participants review the AI information first in Session 1 and the chest X-ray first in Session 2. Sessions are separated by at least four weeks.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 10, 2026

First Posted

June 30, 2026

Study Start

June 30, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

July 6, 2026

Record last verified: 2026-07

Locations