Neuroplasticity in Auditory Aging_Project 2 Aims 1 and 2

Sponsor
University of Maryland, College Park (Other)
Overall Status
Recruiting
CT.gov ID
NCT03475043
Collaborator
National Institute on Aging (NIA) (NIH), National Institutes of Health (NIH) (NIH)
405
1
3
63.2
6.4

Study Details

Study Description

Brief Summary

Millions of elderly adults in the USA have age related hearing loss (ARHL), a malady that affects half of adults 60-69 years, and the majority of older adults. This hearing loss not only impacts communication and functional ability, but also is strongly associated with cognitive decline and decreased quality of life. This project aims to develop effective strategies to compensate and reverse this process through a deeper understanding of plasticity and adaptive auditory function, and how to engage it and harness it to remedy ARHL.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Auditory training: temporal cues
N/A

Detailed Description

The detrimental effects of aging on auditory temporal processing have been well documented in humans and animal models. At present, there are gaps in knowledge of the extent to which these auditory temporal processing deficits can be mitigated in older adults with or without hearing loss through auditory training and neuroplasticity, to improve precision of neural timing and speech understanding. The long-term goal is to determine the extent to which hearing deficits in older adults can be ameliorated with auditory training. The investigators propose an innovative approach to the investigation of aging, hearing, and neuroplasticity by marrying perceptual training experiments with electrophysiological measurements. The objectives are to compare young normal-hearing (YNH), older normal-hearing (ONH), and older hearing-impaired (OHI) adult listeners, and evaluate the improvements in perceptual and electrophysiological measures of temporal processing after explicit training on auditory temporal processing tasks. The central hypothesis is that training of auditory temporal processing will produce concomitant improvements in both perceptual performance and neural encoding, which will close the gap in the age-related differences between groups. The central hypothesis will be tested by pursuing two specific aims: (Aim 1) Determine the extent to which perceptual training on temporal rate discrimination using simple non-speech stimuli improves perceptual and neural encoding in YNH, ONH, and OHI listeners; and (Aim 2) Determine the extent to which perceptual training on the processing of sentences with increasing presentation rate can improve behavioral performance and neural encoding in YNH, ONH, and OHI listeners. The expected outcomes are that the investigators will learn what perceptual training tasks lead to simultaneous improvements in perceptual and neural auditory temporal processing and the findings will produce a significant impact in older listeners who experience difficulty in communicating in daily life because they will lead directly to focused and novel forms of rehabilitation. This research is innovative because the investigators will have established techniques that are proven to provide significant improvements in auditory temporal processing and speech perception, combined with evidence of improvements to neural encoding. These studies will serve the larger goals of the program project grant because they will help identify the neuroplastic mechanisms in the brain of humans that correspond to successful behavioral outcomes in younger and older adults.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
405 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Experimental group Active control group Passive control groupExperimental group Active control group Passive control group
Masking:
Single (Outcomes Assessor)
Masking Description:
Examiners who conduct pre, post, and retention tests with participants do not know to which group a participant is assigned (experimental group, active control group, passive control group).
Primary Purpose:
Health Services Research
Official Title:
Neuroplasticity in Auditory Aging_Auditory Temporal processing_Project 2
Actual Study Start Date :
Feb 21, 2018
Anticipated Primary Completion Date :
May 31, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Auditory training: temporal cues

Aim 1: Listeners will hear target acoustic stimuli that vary in a temporal (timing/duration) cue for 9, 1-hour training sessions and will receive correct-answer feedback. Aim 2: Listeners will hear sentences that vary in speech rate for 6, 1-hour training sessions and will receive correct-answer feedback.

Behavioral: Auditory training: temporal cues
Behavioral training for 6-9 hours in listening to specific characteristics of acoustic signals. Listeners receive correct-answer feedback on each trial.
Other Names:
  • Auditory training: non-temporal cues
  • Active Comparator: Auditory training: non-temporal cues

    Aim 1: Listeners will hear target acoustic stimuli that vary in either stimulus intensity or stimulus frequency during 9, 1-hour training sessions and will receive correct-answer feedback. Aim 2: Listeners will hear speech in varying levels of noise during 6, 1-hour training sessions and will receive correct-answer feedback.

    Behavioral: Auditory training: temporal cues
    Behavioral training for 6-9 hours in listening to specific characteristics of acoustic signals. Listeners receive correct-answer feedback on each trial.
    Other Names:
  • Auditory training: non-temporal cues
  • No Intervention: Passive control group (Aims 1 and 2)

    Listeners will be evaluated on pre-training and post-training tests, but will receive no training at all.

    Outcome Measures

    Primary Outcome Measures

    1. Improvement in behavioral auditory temporal processing measures (Aim 1) [completion of study, approximately 30 months]

      Decrease in threshold (in msec) for discriminating a comparison pulse train to a standard, decrease in cross-over points (in msec) for trained word contrasts, and increase in rate of speech for 50% correct recognition

    2. Improvement in recognition of trained stimuli - fast speech (Aim 2) [completion of study, approximately 24 months]

      Increase in speech rate at which listener maintains 50% and 80% correct recognition

    Secondary Outcome Measures

    1. Change in spectral energy and neural phase locking for trained stimuli (Aim 1) [completion of study, approximately 30 months]

      Increase in spectral energy for pulse trains, cessation of neural phase locking for trained words during silent intervals of the word, and increase in phase-locking factor following training of time-compressed speech, as measured on the Auditory Steady-State Response

    2. Change in phase locking to trained or equivalent stimuli (Aim 2) [completion of study in approximately 24 months]

      Increase in phase-locking factor following training of time-compressed speech, as measured in the frequency-following response

    3. Change in reconstruction accuracy to trained or equivalent stimuli (Aim 2) [completion of study in approximately 24 months]

      Increase in reconstruction accuracy following training of time-compressed speech, as measured with envelope tracking to five-minute speech samples

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • native speaker of English

    • normal cognitive function as measured on Montreal Cognitive Assessment

    • pass screening auditory brainstem response test to make sure they have recordable brainwaves to acoustic stimuli

    • age and hearing sensitivity:

    • young normal-hearing listeners, 18-35 years, hearing thresholds less than 25 decibels (dB) HL from 250 - 4000 Hz;

    • older normal-hearing listeners, 65-85 years, hearing thresholds less than 25 dB HL, from 250-4000 Hz;

    • older hearing-impaired listeners, 65-85 years, with mild-to-moderate, high frequency sensorineural hearing loss;

    • high school diploma

    Exclusion Criteria:
    • absence of conductive hearing loss and middle-ear disease

    • no neurological disease

    • severe or profound hearing loss

    • non-native speaker of English

    • cognitive impairment

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Maryland College Park Maryland United States 20742

    Sponsors and Collaborators

    • University of Maryland, College Park
    • National Institute on Aging (NIA)
    • National Institutes of Health (NIH)

    Investigators

    • Principal Investigator: Sandra Gordon-Salant, Ph.D., University of Maryland

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sandra Gordon Salant, Professor, University of Maryland, College Park
    ClinicalTrials.gov Identifier:
    NCT03475043
    Other Study ID Numbers:
    • UMDCP_P01P2
    • P01AG055365
    First Posted:
    Mar 23, 2018
    Last Update Posted:
    Mar 14, 2022
    Last Verified:
    Feb 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:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 14, 2022