What are the best fitting practices for hearing aids?

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Last updated: November 11, 2025View editorial policy

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Best Fitting Practices for Hearing Aids

Hearing aid fitting should be based on a prescriptive procedure that incorporates individual real-ear measures accounting for each patient's ear-canal acoustics and hearing loss, with verification that amplified speech is comfortably above sensory threshold but below discomfort level across the speech frequency range. 1

Core Fitting Principles

Goal of Amplification

  • The primary objective is to provide maximum access to all acoustic features of speech within an intensity range that is safe and comfortable 1
  • Amplified speech must be comfortably above the patient's sensory threshold but below the level of discomfort across the entire speech frequency range for both ears 1

Essential Pre-Fitting Assessment

  • Hearing aid fitting proceeds optimally when results of physiologic audiological assessment including diagnostic ABR, OAE, and tympanometry are in accord with medical examination 1
  • For infants below developmental age of 6 months, hearing aid selection must be based on physiologic measures alone 1
  • Behavioral threshold assessment with visual reinforcement audiometry should be obtained as soon as possible to cross-check and augment physiologic findings 1
  • A comprehensive audiologic evaluation must include pure-tone testing, word recognition testing, speech-in-noise testing, and loudness discomfort level measures 2

Verification and Validation Protocol

Real-Ear Measurements (Critical)

  • Amplification-device selection, fitting, and verification must be based on a prescriptive procedure that incorporates individual real-ear measures 1
  • Real-ear (microphone verification) measures determine if hearing aids are meeting actual prescriptive targets and can identify under-amplification as a cause of patient dissatisfaction 1

Validation Requirements

  • Validation of amplification benefits, particularly for speech perception, should be examined in both the clinical setting and the child's typical listening environments 1
  • Self-assessment measurement tools such as the Hearing Handicap Inventory for the Elderly (HHIE) or Hearing Handicap Inventory for Adults (HHIA) should be used to determine impact on quality of life 1

Ongoing Monitoring and Adjustment

Regular Follow-Up Schedule

  • Monitoring of amplification requires ongoing audiological assessment along with electroacoustic, real-ear, and functional checks of the hearing instruments 1
  • Periodic evaluations of hearing to monitor stability and evaluation of amplification/assistive listening devices should occur at least annually for adults and children aged >5 years 1
  • More frequent monitoring may be warranted in individuals with fluctuating hearing loss 1
  • For infants and young children, developmental monitoring should occur at regular 6-month intervals 1

Refinement Over Time

  • As hearing loss becomes more specifically defined through audiological assessments and as the child's ear-canal acoustics change with growth, refinement of individual prescriptive hearing-aid gain and output targets is necessary 1
  • Monitoring must include periodic validation of communication, social-emotional, and cognitive development and, later, academic performance to ensure progress is commensurate with the child's abilities 1

Timing Considerations

Prompt Fitting

  • If the family chooses personal amplification, hearing-aid selection and fitting should occur within 1 month of initial confirmation of hearing loss, even when additional audiological assessment is ongoing 1
  • Delay between confirmation of hearing loss and fitting of an amplification device should be minimized 1
  • Audiological habilitation services should be provided by an audiologist who is experienced with these procedures 1

Technology Level Considerations

Evidence on Premium vs. Basic Technology

  • Research demonstrates no statistically significant or clinically important differences in speech understanding improvement or quality of life between premium-level and basic-level hearing aids 3
  • It should not be assumed that more costly hearing aids always produce better outcomes 3
  • Regardless of technology level, comprehensive best-practice fitting protocols should be followed to optimize results for every patient 3

Special Considerations

Complementary Technology

  • Frequency modulation (FM) systems or cochlear implants may be recommended as primary and/or secondary listening devices depending on the degree of hearing loss, goals of auditory habilitation, acoustic environments, and family's informed choices 1

Cochlear Implant Referral Criteria

  • Patients should be referred for cochlear implant evaluation when they have appropriately fit amplification and persistent hearing difficulty with poor speech understanding 1
  • The "60/60" guideline (pure tone average thresholds ≥60 dB and word recognition ≤60%) has 96% sensitivity for identifying cochlear implant candidates 1, 4

Sound Tolerance Issues

  • Problems related to loudness of sounds and reduced sound tolerance can adversely impact adaptation to amplification and quality of life 5
  • A structured assessment tool should be used to evaluate reduced sound tolerance and its impact on hearing aid use 5

Common Pitfalls to Avoid

  • Do not rely on patient self-report alone for determining adequacy of hearing aid fitting, as patients cannot accurately differentiate degree of hearing loss or identify losses requiring intervention 1
  • Avoid under-amplification by confirming prescriptive targets are met through real-ear measurements 1
  • Do not assume infants and young children with well-fit amplification devices will automatically develop auditory skills—ongoing validation is essential 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Audiologic Assessment.

Seminars in hearing, 2022

Guideline

Cochlear Implantation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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