Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:39 PM
Ignite Modification Date:
2025-12-24 @ 11:39 PM
NCT ID:
NCT07246551
Eligibility Criteria:
Inclusion Criteria Patients:
* Newly developed ear discomfort or symptoms within the past month. The patient seeks care at a participating primary care centre and is assessed by a physician because of these ear-related symptoms. Alternatively, for young children: respiratory tract infection with concurrent signs or symptoms suggesting possible ear involvement, even if the child cannot clearly express ear pain.
* Age: Children and adults of all ages are eligible to participate.
* Informed consent: The patient (or guardian for minors) agrees to participate and provides written informed consent. For children under 15 years, consent is obtained from both guardians before any data storage.
* The patient must have been managed by a physician who has consented to participate in the study (as a physician participant) and who is a GP specialist, GP resident, or junior physician (intern or basic training physician) working at the primary care centre.
* At intervention centres, the managing physician must have completed the AOM Diagnosis (Dx) Trainer and reached the required score threshold ("diploma") before including patients.
Inclusion Criteria Physicians:
* General practitioners (GP specialists), GP residents, or junior physicians (interns or basic training physicians) working clinically at participating primary care centres.
* Have provided written informed consent to participate in the study as physician participants.
* At intervention centres, must have completed the AOM Dx Trainer and achieved the required diploma level before patient inclusion.
* At control centres, receive no access to the AOM Dx Trainer during the study period.
Exclusion Criteria:
* Withdrawal of consent by the participant (physician or patient).
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT07246551
Study Brief:
Protocol Section:
NCT07246551