Greater working memory and speech perception scores in cochlear implant users predict better subjective quality of life and hearing

Abstract

A common concern in individuals with cochlear implants (CIs) is difficulty following conversations in noisy environments and social settings. The ability to accomplish these listening tasks relies on the individual working memory abilities and draws upon limited cognitive resources to accomplish successful listening. For some individuals, allocating too much, can result deficits in speech perception and in long term detriments of quality of life. For this study, 31 CI users and NH controls completed a series of online behavioural tests and quality of life surveys, in order to investigate the relationship between visual and auditory working memory, clinical and behavioural measures of speech perception and quality of life and hearing. Results showed NH individuals were superior on auditory working memory and survey outcomes. In CI users, recall performance on the three working memory span tests declined from visual reading span to auditory listening in quiet and then listening in noise and speech perception was predictably worse when presented with noise maskers. Bilateral users performed better on each task compared to unilateral/HA and unilateral only users and reported better survey outcomes. Correlation analysis revealed that memory recall and speech perception ability were significantly correlated with sections of CIQOL and SSQ surveys along with clinical speech perception scores in CI users. These results confirm that hearing condition can predict working memory and speech perception and that working memory ability and speech perception, in turn, predict quality of life. Importantly, we demonstrate that online testing can be used as a tool to assess hearing, cognition, and quality of life in CI users.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Mason Scientific Discovery Fund

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Research Ethics Board of Sunnybrook Health Sciences Centre gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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