Evaluating a Deep Neural Noise-Reduction Algorithm for Hearing Aids

Part of paid clinical trials in West Lafayette, Indiana.

Sponsor
Purdue University
Study ID
NCT07287774
Status
Recruiting

Conditions

  • Hearing Loss, Cochlear

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Hearing Aid Noise Reduction - Off — DEVICE
    No neural noise suppression applied. Baseline processing condition.
  • Hearing Aid Noise Reduction - Low — DEVICE
    Neural noise suppression using the lower-strength algorithm parameters.
  • Hearing Aid Noise Reduction - High — DEVICE
    Neural noise suppression using the higher-strength algorithm parameters.
  • Negative SNR — OTHER
    Noise levels higher than speech levels
  • Zero signal-to-noise ratio — OTHER
    Equal speech and noise levels
  • Positive SNR — OTHER
    Speech levels higher than noise levels

Study Details

This study is designed to understand how different hearing-aid noise-reduction technologies affect a listener's ability to hear speech in noisy environments. Participants will listen to speech at several background-noise levels while trying different processing settings. By comparing performance across these conditions, the study aims to identify which types of noise reduction improve speech intelligibility the most. We expect that some noise-reduction strategies will help listeners understand speech better than others, especially in more difficult listening situations.

Key Dates

Start date
Oct 16, 2025
Status verified
Dec 2025
Primary completion
Apr 30, 2026
Completion
Apr 30, 2026

Study Design

Enrollment
50 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT

Arms

  • Experimental: Hearing Aid Noise-Reduction Processing
    Participants complete all noise-reduction conditions (Off, Low, High) at all tested signal-to-noise ratios in a within-subject crossover design.
  • Experimental: Signal-to-Noise Ratio
    Relative speech and noise levels

Primary Outcome Measure

Immediate Speech Recall [ Time Frame: During a single study visit (approximately 1-2 hours), assessed immediately following presentation of each dual-sentence trial. ]

Locations (1)

FacilityCityStateZIPSite coordinators
Purdue UniversityWest LafayetteIndiana47905
Joshua Alexander, Ph.D.
765-494-5956

Find similar trials in West Lafayette, IN

Related Studies