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AI-assisted Diagnosis, Triage and Assessment of Hearing Loss and Tinnitus

7 de mayo de 2026 actualizado por: Royal Cornwall Hospitals Trust

Artificial Intelligence for the Automated Diagnosis, Triage, and Assessment of Patients With Hearing Loss and Tinnitus: A Pilot Comparative Study With Clinical Evaluation by Otolaryngologists

Hearing loss affects approximately 11 million people in the UK, while tinnitus impacts around 7 million. Both conditions can significantly reduce quality of life and are linked to poorer mental health and employment challenges. Each year, tinnitus alone accounts for more than one million GP appointments, and patients referred to hospital ear, nose and throat (ENT) services often face long delays, sometimes exceeding a year, before their first assessment.

To address this demand, the Royal Cornwall Hospitals NHS Trust has developed a virtual ENT clinic. Patients undergo a validated hearing test in person and complete online questionnaires. Clinicians then review these data to determine next steps, which may include discharge with advice, referral for imaging, or a face-to-face consultation. Initial trials demonstrated that the majority of patients could be managed virtually, substantially reducing waiting times. However, clinicians must still review every case, limiting capacity for patients who require direct care.

This project builds on the virtual clinic by introducing artificial intelligence (AI) to support the assessment process. Using explainable AI methods, the system will be trained to replicate clinician-level decision-making while providing transparent reasoning for its recommendations. The study will evaluate how closely AI-generated outcomes align with clinician assessments, with all cases continuing to receive a clinician's final review. Clinicians will not be aware of the recommendations produced by the AI tool, but the study aims to measure how concordant AI recommendations are with clinician assessments.

If the AI tool's clinical recommendations closely align with clinician recommendations (the gold standard for care), the AI tool could be introduced as a clinical recommendation assistant tool, streamlining the triage and management of hearing loss and tinnitus, enabling clinicians to focus on complex cases, accelerating access to care, and improving efficiency.

Descripción general del estudio

Descripción detallada

BACKGROUND

Hearing loss affects approximately 11 million people in the UK, while tinnitus impacts around 7 million.1,2 Both conditions can significantly reduce quality of life and are linked to poorer mental health and employment challenges.3 Each year, tinnitus alone accounts for more than one million GP appointments, and patients referred to hospital ear, nose and throat (ENT) services often face long delays, sometimes exceeding a year, before their first assessment.4 This was exacerbated even further following the coronavirus (COVID-19) pandemic.5

To address this demand, the Royal Cornwall Hospitals NHS Trust has developed a virtual ENT clinic to manage patients with hearing loss and/or non-pulsatile tinnitus. Patients undergo a validated hearing test in person and complete online questionnaires. Clinicians then review these data to determine next steps, which may include discharge with advice, referral for imaging, or a face-to-face consultation. Inclusion criteria for the virtual clinic for hearing loss and non-pulsatile tinnitus were: ≥16 years of age; subjective bilateral hearing loss and/or tinnitus that did not fulfil the criteria for direct referral to audiology (they would see patients ≥50 years of age); subjective asymmetrical sensorineural hearing loss; and subjective unilateral non-pulsatile tinnitus. Exclusion criteria for the virtual clinic for hearing loss and non-pulsatile tinnitus were: cognitive, motor or visual impairment that may preclude use of an iPad®; patients who had been referred back to ENT having previously been fully medically assessed (redirected to audiology or hearing therapy where appropriate); and symptoms that required a face-to-face appointment (conductive hearing loss, pulsatile tinnitus, vertigo or dizziness, pain, discharge, infections, abnormal ear examination, and history of ear disease, surgery or ear injury).6

Published results demonstrated that most patients could be managed virtually, substantially reducing waiting times.6 However, clinicians must still review every case, limiting capacity for patients who require direct care. This project builds on the virtual clinic by introducing artificial intelligence (AI) to support the assessment process, as a clinical decision support system (CDSS). Using explainable AI methods, the system is trained to replicate clinician-level decision-making while providing transparent reasoning for its recommendations. This retrospective and prospective observational feasibility pilot study aims to evaluate how closely AI-generated outcomes align with clinician assessments, with all cases continuing to receive a clinician's final review. Clinicians will be blind to the recommendations produced by the AI tool, but the study aims to measure how concordant AI recommendations are with clinician assessments.

If the AI tool's clinical recommendations closely align with clinician recommendations (the gold standard for care), the AI tool could be introduced as a clinical recommendation assistant tool, streamlining the triage and management of hearing loss and tinnitus, enabling clinicians to focus on complex cases, accelerating access to care, and improving efficiency.

RATIONALE

The primary rationale for the study is to assess the concordance between AI-generated and clinician-generated outcomes within a real-world virtual hearing loss and tinnitus clinic environment. Demonstrating strong alignment would support the future integration of AI-assisted clinical decision support systems into routine clinical workflows, with the potential to improve service capacity, reduce waiting times, and allow clinicians to focus on more complex cases requiring direct specialist expertise.

In parallel with this work, the research team is undertaking a systematic review examining the use of artificial intelligence in the diagnosis, triage, and management of patients with hearing loss and tinnitus within otolaryngology settings. Although this review has not yet reached the stage of full-text screening, preliminary scoping suggests that, to date, there are no published studies directly evaluating an AI tool used to diagnose, triage, and manage hearing loss and tinnitus patients within an ENT outpatient pathway overseen by otolaryngologists. While the use of AI as a clinical decision support tool is a recognised and growing field, there remains a notable evidence gap in its application to this specific clinical context.

The study design ensures patient safety and ethical integrity by maintaining full clinician oversight for all cases. During this evaluation phase, the AI system will function solely as a research tool and will not influence clinical decision-making, i.e. a shadow implementation. This phased, comparative approach enables a rigorous assessment of feasibility, safety, and acceptability before any consideration of broader clinical implementation.

Ultimately, the findings will help determine whether AI-assisted clinical triage could offer a sustainable and scalable response to rising demand in hearing loss and tinnitus services, enhancing patient access, efficiency, and satisfaction while maintaining the highest standards of clinical care.

THEORETICAL FRAMEWORK

This study is grounded in the intersection of clinical decision-making theory, artificial intelligence (AI) in healthcare, and health systems efficiency models. Its theoretical foundation integrates concepts from evidence-based medicine, human-AI collaboration, and service redesign in healthcare delivery.

  1. Clinical Decision-Making and Diagnostic Reasoning

    Clinical decision-making in otolaryngology involves interpreting complex data from hearing tests, patient histories, and symptom questionnaires to generate diagnostic and management recommendations. According to dual-process theory, clinicians use both analytical (systematic reasoning based on evidence) and non-analytical (pattern recognition and intuition) approaches.7 These cognitive processes underpin expert clinical judgement but are also limited by human variability, cognitive load, and time constraints-particularly in high-demand services within the NHS.

    By modelling clinician decision-making algorithmically, AI systems can emulate these cognitive processes, providing structured, data-driven, explainable recommendations that complement human expertise. This study therefore builds on clinical reasoning theory, assessing whether AI can achieve concordance with clinician judgement within a controlled, supervised framework.

  2. Artificial Intelligence and Explainability in Medicine

    The study applies explainable AI (XAI) principles, which emphasise transparency, interpretability, and accountability in algorithmic decision-making. Traditional "black box" AI models have raised ethical concerns about opacity and trust in clinical contexts. Explainable AI provides interpretable outputs that allow researchers and clinicians to understand why an AI system reached a particular decision, supporting both clinical safety and regulatory compliance.

    This theoretical stance draws on socio-technical systems theory, which views AI not as a replacement for clinicians but as part of an "intervention ensemble approach".8 Within this framework, AI serves as a clinical decision support tool designed to augment human expertise, reduce administrative burden, and enhance diagnostic efficiency, while clinicians retain final authority over all patient care decisions.

  3. Health Systems Efficiency, Virtual Care, and National AI Strategy

This study is grounded in the framework of health service efficiency and equitable access to care. Virtual clinics have already proven effective in reducing waiting times and improving access for patients with hearing loss and tinnitus.6 However, efficiency remains constrained by the requirement for clinicians to personally review every case in detail. Integrating AI-assisted triage models offers a mechanism to streamline this process, supporting clinicians by automating routine assessments while preserving human oversight. This approach aligns with lean healthcare principles, which emphasise reducing non-value-adding steps and directing clinical expertise toward complex or high-risk cases.9

The study also aligns with national healthcare policy promoting digital transformation. The UK Government's "Fit for the Future: 10-Year Health Plan for England" identifies AI and data-driven technologies as central to improving NHS capacity, efficiency, and patient experience through innovation and smarter service delivery.10 In parallel, NHS England's Artificial Intelligence Information Governance Guidance outlines the ethical and governance standards for deploying AI in clinical settings-framing AI as a decision-support tool that complements rather than replaces clinician judgement, ensuring accountability, transparency, and patient trust.11

The integration of AI in this study therefore reflects not only a local initiative to enhance virtual care, but also a broader policy-aligned commitment to digital innovation within the NHS. This framework is informed by the Technology Acceptance Model (TAM), which suggests that successful adoption of new technologies depends on perceived usefulness, ease of integration, and professional trust.12 By evaluating the concordance between AI-generated and clinician-generated outcomes-and later, patient satisfaction-the study contributes empirical evidence on the acceptability, feasibility, and safety of AI-assisted clinical workflows within the NHS.

This study is a prospective and retrospective observational mixed-methods service evaluation study, with elements of a diagnostic accuracy and implementation evaluation framework.

Tipo de estudio

De observación

Inscripción (Estimado)

1500

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Neil C Tan, MEd PhD FRCS(ORL-HNS)
  • Número de teléfono: +441872 253404
  • Correo electrónico: neil.tan@nhs.net

Copia de seguridad de contactos de estudio

  • Nombre: Christian JW Grimes, BMBS MRCS (ENT) PGCert ClinEd
  • Número de teléfono: +447970780502
  • Correo electrónico: christian.grimes@nhs.net

Ubicaciones de estudio

    • Cornwall
      • Truro, Cornwall, Reino Unido, TR1 1LJ
        • Treliske Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

The study population comprises adult patients managed through the virtual hearing loss and tinnitus clinic, in the Ear, Nose and Throat Department at the Royal Cornwall Hospitals Trust. Patients included are seen in the virtual clinic during the study period, as well as clinical staff involved in reviewing and making decisions within the service. Patient data are analysed observationally, and a subset of patients and clinicians may be invited to provide questionnaire or interview data to explore experiences of the AI-assisted clinic. Patients will comprise of those living in the county of Cornwall and considered under the care of the Royal Cornwall Hospitals Trust.

Descripción

Inclusion Criteria:

  • Patients assessed in the RCHT virtual hearing loss and tinnitus clinic.
  • Presenting symptoms of hearing loss and/or tinnitus.
  • Ability to provide informed consent to participate in the study.

Exclusion Criteria:

  • Individuals under 18 years of age.
  • Patients unable to provide informed consent.
  • Patients without sufficient English proficiency where translation services cannot be arranged.
  • Cases where data quality is insufficient for analysis.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Phase 1 - Patients undergoing the standard virtual hearing loss and tinnitus clinic
Phase 1 consists of a retrospective and prospective observational evaluation of consecutive adult patients managed through the virtual hearing loss and tinnitus clinic at the Royal Cornwall Hospitals Trust, between August 2025 and August 2026. No additional interventions.
An explainable AI-based clinical decision support tool within an existing virtual hearing loss and tinnitus clinic. The tool provides non-binding triage and investigation recommendations based on routinely collected patient data, with all final clinical decisions remaining the responsibility of the clinician and no change to standard care pathways
Phase 2 - Patients undergoing the AI-assisted virtual hearing loss and tinnitus clinic
Phase 2 consists of a prospective observational evaluation of consecutive adult patients managed through the AI-assisted virtual hearing loss and tinnitus clinic at the Royal Cornwall Hospitals Trust, between August 2026 and August 2027. The AI-assisted clinic is the intervention.
An explainable AI-based clinical decision support tool within an existing virtual hearing loss and tinnitus clinic. The tool provides non-binding triage and investigation recommendations based on routinely collected patient data, with all final clinical decisions remaining the responsibility of the clinician and no change to standard care pathways
Phase 2 - Staff involved in providing an AI-assisted virtual hearing loss and tinnitus clinic
Staff involved in running the artificial intelligence-assisted virtual hearing loss and tinnitus clinic at the Royal Cornwall Hospitals Trust from August 2026 to August 2027. They include doctors, healthcare assistants, administrative staff and nurses. The AI-assisted clinic is the intervention.
An explainable AI-based clinical decision support tool within an existing virtual hearing loss and tinnitus clinic. The tool provides non-binding triage and investigation recommendations based on routinely collected patient data, with all final clinical decisions remaining the responsibility of the clinician and no change to standard care pathways

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
MRI internal auditory meatus (IAM) referral recommendation
Periodo de tiempo: March 2026 - August 2026

Agreement between the clinical outcomes generated by the AI clinical decision support system and the clinician-derived "gold standard" outcomes within the virtual hearing loss and tinnitus clinic. Agreement will be evaluated for:

MRI internal auditory meatus (IAM) referral recommendation (binary outcome: yes/no). Agreement will be quantified using sensitivity and specificity with 95% confidence intervals, derived from contingency tables and one-vs-rest analyses for categorical outcomes, as specified in the statistical analysis plan.

March 2026 - August 2026
Clinical triage outcome
Periodo de tiempo: March 2026 - August 2026

Agreement between the clinical outcomes generated by the AI clinical decision support system and the clinician-derived "gold standard" outcomes within the virtual hearing loss and tinnitus clinic. Agreement will be evaluated for: Clinical triage outcome (categorical outcome: refer to face-to-face ENT clinic, refer to audiology, refer to audiology plus hearing therapy, or discharge).

Agreement will be quantified using sensitivity and specificity with 95% confidence intervals, derived from contingency tables and one-vs-rest analyses for categorical outcomes, as specified in the statistical analysis plan.

March 2026 - August 2026

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Patient experience and satisfaction with the AI-assisted virtual hearing loss and tinnitus clinic
Periodo de tiempo: August 2026 - August 2027

Patient experience and satisfaction with the AI-assisted virtual hearing loss and tinnitus clinic, assessed using structured satisfaction questionnaires administered by telephone. Outcomes will include:

Quantitative measures (e.g. Likert-scale ratings of confidence, satisfaction, and acceptability), and

Qualitative data from open-ended responses and semi-structured interviews, analysed using a directed content analysis informed by the NASSS framework.

August 2026 - August 2027
Staff experience, usability, and acceptability of the AI-assisted clinical decision support system
Periodo de tiempo: August 2026 - August 2027
Staff experience, usability, and acceptability of the AI-assisted clinical decision support system, explored through qualitative interviews with clinicians and relevant stakeholders involved in delivering or implementing the virtual clinic pathway.
August 2026 - August 2027

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

30 de mayo de 2026

Finalización primaria (Estimado)

13 de agosto de 2026

Finalización del estudio (Estimado)

31 de agosto de 2027

Fechas de registro del estudio

Enviado por primera vez

7 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de mayo de 2026

Publicado por primera vez (Actual)

14 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

14 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

7 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

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INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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