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Clinical Trial 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.


Clinical Trial Description

Audiologic rehabilitation aims to improve communication for people with hearing impairment. Education is widely regarded as an integral part of rehabilitation, but the effect of the delivery method of an educational program on the experience of hearing problems has rarely been investigated in controlled trials. Internet as a complement to audiological rehabilitation has been tested in different studies with promising results. Though, until now not applied clinically as a part of an audiological rehabilitation, focused on hearing aid users with persistent self- reported activity limitation and participation restriction.

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

Hearing aid users will randomly be assigned to an intervention group or a control group. The intervention group is going to have access to a book and to a prepared compendium about communication strategies via the Internet and will receive weekly topic-based reading instructions related to the different chapters of the book or the compendium. The group will also have access to online and telephone support and access to an online discussion forum where new discussion topics will be posted each week. The project leader will evaluate the weekly data via the Internet. The control group will only have access to the book's content via the Internet and will be asked to read and evaluate the content.

The Hearing Handicap Inventory for the Elderly, the Communication Strategies Scale, the Hospital Anxiety and Depression Scale, and the International Outcome Inventory for Hearing Aids will be used to measure the outcomes of this study. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT01837550
Study type Interventional
Source Sodra Alvsborgs Hospital
Contact
Status Completed
Phase N/A
Start date April 2013
Completion date June 2014

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