Stream Segregation and Speech Recognition in Noise in Individuals With Cochlear Implants

Sponsor
Father Flanagan's Boys' Home (Other)
Overall Status
Recruiting
CT.gov ID
NCT04854031
Collaborator
(none)
30
1
14.9
2

Study Details

Study Description

Brief Summary

Individuals with cochlear implants will complete tasks which measure auditory resolution, working memory, stream segregation, and speech recognition in the presence of competing speech using their everyday clinical device settings. The relationship between these tasks will be examined to identify the factors which predict successful speech recognition in the presence of competing speech.

Condition or Disease Intervention/Treatment Phase
  • Device: Cochlear Implants

Detailed Description

Individuals with cochlear implants struggle to understand speech in the presence of competing talkers because they have trouble segregating auditory streams. The premise of this project is that individual differences in auditory resolution and cognitive ability across individuals with cochlear implants determine the extent to which they can segregate auditory streams from one another and hear out target speech embedded in competing talkers. Our goal is to test whether the link between speech recognition in noise and individual differences in auditory resolution and working memory in individuals with cochlear implants is due to the limitations that these individual differences place on stream segregation. The outcome measure to be predicted is sentence recognition in two-talker babble. Previous work has found that spectral and temporal modulation detection thresholds (measures of auditory resolution) and performance on the reading span task (a measure of working memory that is closely linked to fluid intelligence) are predictors of speech recognition in quiet. To account for these sources of variability in speech recognition, we will verify that these tasks jointly predict individual differences in sentence recognition in quiet. Adding competing talkers during the speech recognition task will introduce additional variability beyond the variability of speech recognition in quiet. We hypothesize that this additional variability with competing talkers should be predicted by individual differences in stream segregation ability, which will in turn be predicted by auditory resolution and working memory. Obligatory and voluntary stream segregation ability will be measured using rapidly presented digit sequences manipulated to have alternating fundamental frequencies (F0) for each digit. Participants will resist integration and repeat back only the digits presented with the higher F0. The magnitude of the F0 alternation will be manipulated to control the difficulty of segregating streams. The predicted relationship between stream segregation and sentence recognition will be tested for auditory resolution and working memory in independent and combined models. Completing this goal will identify the auditory and cognitive factors that support stream segregation in post-lingually deafened adults with cochlear implants. This identification will enable development of cochlear implant design and rehabilitation strategies to facilitate stream segregation in these patients as well as investigation of the developmental trajectories of these factors in children with cochlear implants. We plan to implement this study in at-home testing conditions to avoid risking COVID transmission in the lab, so this work will also determine the feasibility of at-home testing of individuals with cochlear implants. At-home testing would expand the amount and diversity of participants we are able to recruit for future studies.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Stream Segregation and Speech Recognition in Noise in Individuals With Cochlear Implants
Actual Study Start Date :
Aug 2, 2021
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Oct 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Cochlear Implant Recipients

30 participants who lost their hearing and received one or two cochlear implants as adults will participate in this study. We will include unilaterally and bilaterally implanted individuals listening with their everyday hearing configuration. Individuals with residual acoustic hearing better than 60 dBA at any audiometric frequency will be excluded. Participants will range in age between 19 and 80 years old, although most are expected to be within 50 - 75 years of age.

Device: Cochlear Implants
Individuals with cochlear implants will be tested on their hearing ability. Auditory recordings of speech will be played to participants from a loudspeaker. Recordings will be edited to add competing noise sources and to adjust talker voice pitch. Synthetic sounds will be manipulated to control auditory cue salience in detection tasks.

Outcome Measures

Primary Outcome Measures

  1. Speech Recognition [Up to 1 hour]

    The metric for speech recognition will be the proportion of target sentence keywords correctly repeated in order

  2. Working Memory [Up to 2 hours]

    The metrics for working memory will be the total number of memoranda recalled in each task

  3. Auditory cue detection [Up to 1 hour]

    The metric for auditory cue detection will be the magnitude of the cue which the participant can detect 71% of the time.

  4. Stream Segregation [Up to 1 hour]

    The metric for stream segregation will be the change in target digit recall that occurs with differences in voice pitch between target and distractor digits.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Has at least one cochlear implant.

  • Lost their hearing during adulthood.

  • Native English speaker.

Exclusion Criteria:
  • Cognitive impairment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Boys Town National Research Hospital Omaha Nebraska United States 68131

Sponsors and Collaborators

  • Father Flanagan's Boys' Home

Investigators

  • Principal Investigator: Adam K Bosen, Father Flanagan's Boys' Home

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Adam Bosen, Director, Auditory Perceptual Encoding Laboratory, Father Flanagan's Boys' Home
ClinicalTrials.gov Identifier:
NCT04854031
Other Study ID Numbers:
  • 5P20GM109023-07
First Posted:
Apr 22, 2021
Last Update Posted:
Mar 8, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes

Study Results

No Results Posted as of Mar 8, 2022