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Evaluation of the Effect of a Spatial Localization Training Program on Auditory Comprehension

Evaluation of the Effect of a Spatial Localization Training Program on Auditory Comprehension in Noise in Bi-implanted Subjects With Post-lingual Deafness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05237180
Acronym
CAudiBruit
Enrollment
12
Registered
2022-02-14
Start date
2022-02-15
Completion date
2022-03-01
Last updated
2022-10-20

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

Conditions

Hearing Loss, Cochlear

Brief summary

Hearing comprehension under complex listening conditions is considered to be the central complaint of everyday life for patients with cochlear implants. Localization is one of the cues for listening comprehension. However, only few studies have investigated the effect of spatial localization training on listening comprehension performance in noise. None of these studies correspond to the desire to purpose training by speech therapists while using affordable equipment. The main objective of this study is to evaluate the effect of a spatial localization training protocol in cochlear bi-implanted subjects with post-lingual deafness on their ability to understand in noise. 2 groups of 10 subjects each will be recruited: a patient group and a control group. The patient group will undergo 8 sessions of spatial localization rehabilitation lasting an average of 45 minutes each. After this programme, the pre-test and post- test results obtained will be compared.

Interventions

OTHERspatial localisation training

8 spatial localization training sessions MBAA and SSQ tests before and after training sessions.

Sponsors

Centre Hospitalier Universitaire de la Réunion
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* post-lingual deafness * implanted bilaterally for at least 1 year * score ≥ 70 at LAFON scale * score ≥ 70 at MBAA scale * score ≥ 5/9 at CAP scale * good command of the French language * accepts to participate in the study

Exclusion criteria

* do not realize speech reeducation (spatial localisation and speech perception) during the study * no change in setting of cochlear implants

Design outcomes

Primary

MeasureTime frameDescription
Change of Hearing comprehension performance in noise10 weeks after inclusionMBAA (Marginal Benefic from Acoustical Amplification) scale. Minimal score = 0 and maximal score =540. minimum score means that the patient is unable to repeat phrases and maximal score means that the patient is able to repeats all phrases.

Countries

Reunion

Outcome results

None listed

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