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N/A N=74 Randomized Single-blind Supportive Care

Educational Program for Hearing Aid Users With Internet Support

Hearing Impaired

Enrolled (actual)
74
Serious AEs
0.0%
Results posted
Apr 2016
Primary outcome: Primary: The Hearing Handicap Inventory for the Elderly (HHIE) — 42.0; 36.1; 35.8; 31.3 units on a scale — p=0.685

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Intervention group (Behavioral); Control group (Behavioral)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
Sodra Alvsborgs Hospital
Primary completion
Dec 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
The Hearing Handicap Inventory for the Elderly (HHIE)
42.0; 36.1; 35.8; 31.3; 36.0; 34.0 0.685
SECONDARY
International Outcome Inventory for Hearing Aids (IOI-HA)
4.1; 4.4; 3.8; 4.1; 3.1; 3.1
SECONDARY
Hospital Anxiety and Depression Scale (HADS)
8.5; 7.4; 7.5; 6.5; 4.8; 6.8
SECONDARY
Communication Strategies Scale (CSS)
68.1; 67.2; 74.7; 68.5; 70.9; 66.7

Summary

The purpose of this study is to examine the short-term effects of complementing an educational program for hearing aid users with Internet support.

Eligibility Criteria

Inclusion Criteria

  • the hearing aid users to be between 20 and 80 yr of age,
  • the hearing aid users to have conductive or sensorineural hearing loss of mild to moderate degree (20-60 decibel Hearing Level pure-tone average measured across 500, 1000, and 2000 Hertz),
  • the hearing aid users to have completed a hearing aid fitting at least 3 months before the study began (regardless of hearing aid manufacturer, model, or hearing aid outcomes),
  • the hearing aid users to have a Hearing Handicap Inventory for the Elderly (HHIE) score of >20 points (indicative of some residual self-reported hearing problems),
  • the hearing aid users to provide informed consent to participate

Exclusion Criteria

  • the hearing aid users who are not fulfilling the conditions to participate
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01837550). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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