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AI and blood tests aim to predict hearing loss in seniors

NCT ID NCT07612618

Knowledge-focused Sponsor: Chinese PLA General Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to create a tool that predicts age-related hearing loss using artificial intelligence and blood samples. Researchers will analyze 15 years of data from 1,000 older adults and also test 100 seniors for proteins linked to memory problems. The goal is to identify risks early and help prevent both hearing loss and dementia.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 1,000 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

This study enrolls community-dwelling adults aged ≥60 years from multiple Chinese centers. Inclusion: occupational noise exposure, longitudinal pure-tone audiometry, complete clinical data. Exclusion: non-age/noise hearing loss (e.g., otitis media, otosclerosis, Meniere's disease), missing data \>20%, severe mental/cognitive impairment. The prospective cohort (n=100) recruited from community health centers in North and East China. Inclusion: permanent local residents (≥9 months/year), able to complete assessments, WHO ARHL criteria (PTA≥25 dB HL), written consent. Exclusion: severe psychiatric disorders, major organ failure (NYHA III-IV, eGFR\<30), life expectancy \<3 years, non-ARHL loss, diagnosed dementia, Parkinson's, stroke with severe sequelae, or other unsuitable conditions. Prospective participants followed at baseline, 12 months. Among them, 50 ARHL with cognitive impairment (MoCA\<26) and 50 with ARHL+normal cognition (MoCA≥26) receive proteomics analysis for biomarker discovery

Ages

60 to 100 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Age ≥ 60 years; 2. Availability of longitudinal pure-tone audiometry data; 3. Documented history of occupational noise exposure; 4. Complete clinical data (including past medical history and medication history). Exclusion Criteria: 1. Hearing loss caused by non-age or non-noise factors (e.g., otitis media, otosclerosis, Meniere's disease); 2. Missing clinical data \>20%; 3. Concurrent severe mental illness or cognitive impairment (unable to complete audiological assessment).

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Conditions

The condition(s) this trial relates to.

Cognitive Dysfunction presbycusis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Age related hearing loss

How to take part

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  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

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More trials for these conditions

Other studies related to the condition(s) this trial covers.