SPAT_AI: Development and Evaluation of an Artificial Intelligence Model for the Diagnosis of Aeroallergies

Sponsor
Hippocreates (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05918354
Collaborator
(none)
1,000
2
10
500
49.9

Study Details

Study Description

Brief Summary

To improve accuracy and take out human error, Hippo Dx previously developed S.P.A.T., an automated skin prick test. Now, Hippo Dx will develop and evaluate a S.P.A.T. artificial intelligence (AI) medical software to support physicians in the read out of the test results from an automated skin prick test.

In this study 700 images will be collected to develop the AI model, an additional 200 images will be collected to evaluate performance of the AI model. In a last independent cohort of 100 patients, performance of read-out by the physician will be compared with read out by the physician supported by the S.P.A.T. AI medical software.

The primary endpoint is the accuracy of the maximal wheal size measurement by S.P.A.T. AI versus the maximal wheal size measurement by the physician.

It is a prospective multicentric study that will include 1000 study participants from different countries.

Condition or Disease Intervention/Treatment Phase
  • Device: Skin Prick Automated Test

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Development and Evaluation of an Artificial Intelligence Model to Support Read Out of Skin Prick Automated Test Results for the Diagnosis of Aeroallergies
Anticipated Study Start Date :
Jun 30, 2023
Anticipated Primary Completion Date :
Dec 30, 2023
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Allergy

Adults aged 18 years or above, consulting the outpatient clinic for an allergy diagnosis to aeroallergens with skin prick automated test device.

Device: Skin Prick Automated Test
Detection of sensitisation to specific allergens via the skin prick automated test.

Outcome Measures

Primary Outcome Measures

  1. Equivalency of S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    The equivalency of the maximal wheal diameter as measured by S.P.A.T. AI versus the maximal wheal diameter as assessed by the physician.

Secondary Outcome Measures

  1. Precision of S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    Likelihood that the S.P.A.T. AI maximal wheal diameter measurement lays within the range of the maximal wheal size measurement of 3 independent physicians.

  2. Intra-reader variability of S.P.A.T. read out by physicians [15 minutes after the diagnostic test]

    Variation in maximal wheal size diameter of the same image by 3 independent physicians.

  3. Comparison of different methods (maximal wheal diameter) of read out by S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    Accuracy of the maximal wheal diameter by S.P.A.T. AI versus the maximal wheal diameter measurement by the physician.

  4. Comparison of S.P.A.T. artificial intelligence supporting the physician versus physician [15 minutes after the diagnostic test]

    Inter-reader variability of read out of S.P.A.T. results by the physician supported by the S.P.A.T. AI software versus the physician alone.

  5. Time impact of S.P.A.T. artificial intelligence supporting the physician versus physician [15 minutes after the diagnostic test]

    Total time required to perform read out of S.P.A.T. results by the physician supported by the S.P.A.T. AI software versus the physician alone.

  6. Comparison of different methods (mean - maximal wheal diameter) of read out by S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    Accuracy of mean wheal diameter by S.P.A.T. AI versus the maximal wheal diameter measurement by the physician.

  7. Comparison of different methods (wheal area - maximal wheal diameter) of read out by S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    Accuracy of wheal area by S.P.A.T. AI versus the maximal wheal diameter measurement by the physician.

  8. Comparison of different methods (HEP index - maximal wheal diameter) of read out by S.P.A.T. artificial intelligence versus physician [15 minutes after the diagnostic test]

    Accuracy of HEP-index measurement by S.P.A.T. AI versus the maximal wheal diameter measurement by the physician.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults aged 18 years or above, consulting the outpatient clinic for an allergy diagnosis to aeroallergens will be included.
Exclusion Criteria:
  • Skin pathology like chronic or exuberant urticaria, dermographism, chronic dermatitis that needs daily treatment

  • Use of antihistaminic medication < 7 days before the start of the study

  • Use of tricyclic antidepressants (antihistamine activity) < 7 days before the start of the study

  • Use of topical corticoids on the forearm < 7 days before the start of the study

  • Use of Omalizumab < 6 months before the start of the study

  • Pregnancy: there is a remote possibility of inducing a systemic allergic reaction that could induce uterine contractions or necessitate the use of epinephrine (thought to cause constriction of the umbilical artery)

  • Incapacitated individuals

  • Individuals who do not speak the local language (Dutch - French)

  • Individuals who cannot read or write

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinique Universitaires Saint-Luc Brussels Belgium 1200
2 UZ Leuven Leuven Belgium 3000

Sponsors and Collaborators

  • Hippocreates

Investigators

  • Principal Investigator: Mark Jorissen, MD, PhD, UZ Leuven

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hippocreates
ClinicalTrials.gov Identifier:
NCT05918354
Other Study ID Numbers:
  • HDX003
First Posted:
Jun 26, 2023
Last Update Posted:
Jun 26, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 26, 2023