- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03212924
Listening Effort in Cochlear Implant Users
August 21, 2018 updated by: Oticon Medical
Evaluation of Listening Effort With Pupillometry in Cochlear Implant Users
Listening with a cochlear implant remains difficult and most listeners will report high levels of listening effort.The present study is a "pilot" aiming to evaluate listening effort for cochlear implant users.
The listening effort is measured with pupillometry, by monitoring the variations of pupil size in response to different stimuli.
The size of the pupil is known to increase with the listening effort.
The listening effort is evaluated in two different situation: speech perception in quiet and speech perception in noise.
The pupillometry measures will be compared for the two listening conditions.
Moreover, the study will evaluate the relationship between objective (pupil dilatation) and subjective measures (auto evaluation) of listening effort, and between speech comprehension, cognitive abilities and listening effort.
Study Overview
Status
Completed
Conditions
Detailed Description
Nowadays, cochlear implants (CI) are successfully used to rehabilitate severe to profound sensorineural hearing loss.
Most CI users can understand speech in quiet, but comprehension scores drop in the presence of background noise and in adverse conditions.
Listening with a cochlear implant remains very demanding and most listeners report high levels of listening effort.
The aim of current auditory prostheses and cochlear implants is not only restore speech understanding, but also to restore all the cognitive functions that are associated to a listening task (e.g., memory, executive functions, attention).
Evaluating the listening effort is a new way to assess the efficiency of the hearing aids or cochlear implants.
The listening effort indicates the amount of cognitive resources that are dedicated to a listening task; it evaluates also the cognitive resources remaining available for the other cognitive functions.
The present study is a "pilot" aiming to evaluate listening effort for cochlear implant users.
The listening effort is measured with pupillometry, i. e. by measuring the pupil dilatation in response to different stimuli.
The size of the pupil is known to increase with the listening effort.
The listening effort is evaluated in two different situation: speech perception in quiet and speech perception in noise.
Speech comprehension is measured for the two listening conditions and cognitive functions are assessed by the MOCA (Montreal Cognitive Assessment).
In addition, the subjects are asked to subjectively evaluate the amount of listening effort they used in each listening situation.
The pupillometry measures will be compared for the two listening conditions.
Moreover, the study will evaluate the relationship between objective (pupil dilatation) and subjective measures (self evaluation) of listening effort, and between speech comprehension, cognitive abilities and listening effort.
Study Type
Interventional
Enrollment (Actual)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Paris, France, 75013
- Hôpital Pitié Salpétrière - APHP
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 66 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- informed consent
- Native French speaker or fluent French speaker
- Patient already fitted with one or two cochlear implants Oticon Medical
- Can correctly identify at least 10 % of the words in monosyllabic Lafon lists in quiet
- Normal or corrected to normal vision
Exclusion Criteria:
- vulnerable patients (kids, pregnant women, persons under guardianship)
- No Social security affiliation
- blindness
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pupillometry
Measure of pupil dilatation while listening to speech (monosyllabic words) in quiet and in noise. Evaluation of speech comprehension in quiet Evaluation of speech comprehension in noise Measure of cognitive functions with the MOCA (Montreal Cognitive Assessment) Auto evaluation of listening effort in quiet Auto evaluation of listening effort in noise |
Measure of pupil dilatation simultaneously to the evaluation of speech intelligibility.
The variation of the pupil size is monitored during the presentation of speech stimuli in quiet and in the presence of a background noise.
Three lists of 17 monosyllabic words (Lafon) are presented in quiet at 65 dB SPL.
Listeners have to repeat what they understood.
The results correspond to the percent of phonemes correctly identified.
Three lists of 17 monosyllabic words (Lafon) are presented in a wide band noise at 65 dB SPL with a SNR (signal to noise ratio) of +10 dB.
Listeners have to repeat what they understood.
The results correspond to the percent of phonemes correctly identified.
The Montreal Cognitive Assessment (MoCA) is a screening instrument to detect cognitive dysfunction.
It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.
The time to administer the MoCA is approximately 10 minutes.
The total possible score is 30 points.
The test suggests the existence of a cognitive impairment if the participant scores less than 26 points.
The test is presented on a single sheet of paper.
Other Names:
The participant has to represent, on a continuous line, the amount of listening effort he used when listening to the monosyllabic words presented in quiet.
A score from 0 (no listening effort) to 10 (effort maximum) is extracted from his response.
Other Names:
The participant has to represent, on a continuous line, the amount of listening effort he used when listening to the monosyllabic words presented in the background noise.
A score from 0 (no listening effort) to 10 (effort maximum) is extracted from his response.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pupil dilatation (mm)
Time Frame: 1 hour
|
The listening effort while listening to speech stimuli is estimated by measuring the pupil size relative to a baseline.
Measures of pupil dilatation are compared between quiet and noisy conditions (+ 10 SNR: signal to noise ratio).
|
1 hour
|
|
Amplitude of peak of pupil dilatation
Time Frame: 1 hour
|
The listening effort while listening to speech stimuli is estimated by measuring the pupil size relative to a baseline.
The peak is defined as the point in time where the maximum of pupil dilatation occurs.
The amplitude of the peak of dilatation is compared between quiet and noisy conditions (+ 10 SNR: signal to noise ratio).
|
1 hour
|
|
Latency of peak of pupil dilatation (ms)
Time Frame: 1 hour
|
The listening effort while listening to speech stimuli is estimated by measuring the pupil size relative to a baseline.
The peak is defined as the point in time where the maximum of pupil dilatation occurs.
The latency of the peak of dilatation is compared between quiet and noisy conditions (+ 10 SNR: signal to noise ratio).
|
1 hour
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech intelligibility in quiet
Time Frame: 30 mins simultaneously to pupillometry measures
|
percentage of phonemes correctly identify when the speech stimuli (monosyllabic words of Lafon) are presented in quiet at 65 dB SPL
|
30 mins simultaneously to pupillometry measures
|
|
Speech intelligibility in noise
Time Frame: 30 mins simultaneously to pupillometry measures
|
percentage of phonemes correctly identify when the speech stimuli (monosyllabic words of Lafon) are presented in a wide band noise at 65 dB SPL with a +10 dB SNR (signal to noise ratio)
|
30 mins simultaneously to pupillometry measures
|
|
MOCA (Montreal Cognitive assessment)
Time Frame: 15 mins
|
Score at the MOCA.
The maximum score is 30.
The test suggests the existence of a cognitive impairment if the score is lower than 26.
|
15 mins
|
|
VAS quiet
Time Frame: 1 min
|
Auto evaluation of the listening effort in quiet with Visual Analog Scale.
The participant has to indicate, on a continuous line, the listening effort used in the quiet condition.
A score from 0 (no effort) to 10 (maximum effort) is extracted from the VAS.
|
1 min
|
|
VAS noise
Time Frame: 1 min
|
Auto evaluation of the listening effort in quiet with Visual Analog Scale.
The participant has to indicate, on a continuous line, the listening effort used in the noise condition.
A score from 0 (no effort) to 10 (maximum effort) is extracted from the VAS.
|
1 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Isabelle Mosnier, MD, Hôpital Pitié Sapêtrière - APHP
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Kramer SE, Teunissen CE, Zekveld AA. Cortisol, Chromogranin A, and Pupillary Responses Evoked by Speech Recognition Tasks in Normally Hearing and Hard-of-Hearing Listeners: A Pilot Study. Ear Hear. 2016 Jul-Aug;37 Suppl 1:126S-35S. doi: 10.1097/AUD.0000000000000311.
- Steel MM, Papsin BC, Gordon KA. Binaural fusion and listening effort in children who use bilateral cochlear implants: a psychoacoustic and pupillometric study. PLoS One. 2015 Feb 10;10(2):e0117611. doi: 10.1371/journal.pone.0117611. eCollection 2015. Erratum In: PLoS One. 2015;10(10):e0141945.
- Winn MB, Edwards JR, Litovsky RY. The Impact of Auditory Spectral Resolution on Listening Effort Revealed by Pupil Dilation. Ear Hear. 2015 Jul-Aug;36(4):e153-65. doi: 10.1097/AUD.0000000000000145.
- Koelewijn T, Zekveld AA, Festen JM, Kramer SE. Pupil dilation uncovers extra listening effort in the presence of a single-talker masker. Ear Hear. 2012 Mar-Apr;33(2):291-300. doi: 10.1097/AUD.0b013e3182310019.
- Zekveld AA, Kramer SE. Cognitive processing load across a wide range of listening conditions: insights from pupillometry. Psychophysiology. 2014 Mar;51(3):277-84. doi: 10.1111/psyp.12151. Epub 2014 Feb 9.
- Zekveld AA, Heslenfeld DJ, Johnsrude IS, Versfeld NJ, Kramer SE. The eye as a window to the listening brain: neural correlates of pupil size as a measure of cognitive listening load. Neuroimage. 2014 Nov 1;101:76-86. doi: 10.1016/j.neuroimage.2014.06.069. Epub 2014 Jul 3.
- Zekveld AA, Kramer SE, Festen JM. Cognitive load during speech perception in noise: the influence of age, hearing loss, and cognition on the pupil response. Ear Hear. 2011 Jul-Aug;32(4):498-510. doi: 10.1097/AUD.0b013e31820512bb.
- Zekveld AA, Kramer SE, Festen JM. Pupil response as an indication of effortful listening: the influence of sentence intelligibility. Ear Hear. 2010 Aug;31(4):480-90. doi: 10.1097/AUD.0b013e3181d4f251.
- Pals C, Sarampalis A, Baskent D. Listening effort with cochlear implant simulations. J Speech Lang Hear Res. 2013 Aug;56(4):1075-84. doi: 10.1044/1092-4388(2012/12-0074). Epub 2012 Dec 28.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 19, 2017
Primary Completion (Actual)
March 27, 2018
Study Completion (Actual)
March 27, 2018
Study Registration Dates
First Submitted
July 6, 2017
First Submitted That Met QC Criteria
July 6, 2017
First Posted (Actual)
July 11, 2017
Study Record Updates
Last Update Posted (Actual)
August 22, 2018
Last Update Submitted That Met QC Criteria
August 21, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PIC_13
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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