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Validation of uHear™ as a Screening Tool to Detect Hearing Impairment in Elderly Cancer Patients Within a Comprehensive Geriatric Assessment

Validation of uHear™ as a Screening Tool to Detect Hearing Impairment in Elderly Cancer Patients Within a Comprehensive Geriatric Assessment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02381782
Acronym
UHEAR
Enrollment
33
Registered
2015-03-06
Start date
2014-12-31
Completion date
2015-06-30
Last updated
2018-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Hearing Loss

Brief summary

Over the last few years, there has been a considerable interest in the development of screening tools to assess the capability of elderly cancer patients to tolerate anti-cancer treatment. Therefore, the NCCN Guidelines in Senior Adult Oncology recommend an assessment of co-morbid conditions that are likely to interfere with cancer treatment and tolerability. As presbyacusis is common in an older population, elderly cancer patients are at high risk for social isolation and a reduced quality of life. Therefore, in this project the investigators aim to validatie uHear™ as a quick and reliable screening tool to screen for presbyacusisf in routine clinical oncology practice.

Interventions

None listed

Sponsors

General Hospital Groeninge
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients should have reached the age of 70 or more at enrolment * Histologically confirmed diagnosis of solid cancer or hematologic malignancy. All stages of cancer are eligible * Patients should be fluent in Dutch or French * Patients must receive their primary oncology care in the participating hospital * Patients should be cognitively capable of performing the audiology assessment * Patients should have signed informed consent

Exclusion criteria

* Patients who do not match the above inclusion criteria * Patients who are visiting the oncology clinic for a second opinion and do not wish to be treated in this clinic * Patients presenting with clinically diagnosed Ménière's disease, retrocochlear hearing loss, autoimmune inner ear disease, fluctuating hearing loss or a history of sudden sensory neural hearing loss * Patients who already have a hearing aid or a previously diagnosed hearing loss

Design outcomes

Primary

MeasureTime frame
Validation of uHear™ as a screening tool to detect hearing loss in elderly cancer patientsBaseline

Secondary

MeasureTime frame
To determine the prevalence of presbyacusis in an elderly cancer populationBaseline
To compare objective and subjective hearing screening measuresBaseline
To measure hearing impairment in G8 positive patients compared with G8 negative patientsBaseline
To compare uHear™ with the Whispered Voice TestBaseline
To evaluate the use of uHear™ as a measure to determine eligibility for cisplatin treatment in elderly cancer patientsBaseline

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026