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Clinical Trial Summary

This RCT will have two arms: A control group that receives the standard of care from audiologists and an experimental group that receives both the standard of care and the at-home use of the TELLYHealth intervention. Subjects in each group will complete questionnaires at enrollment, mid-study and at the end of the study.


Clinical Trial Description

HTM will develop the "TELLYHealth (tm) system" that will provide education on hearing aid use and maintenance. HTM will conduct a randomized controlled trial (RCT) to quantify the benefits of TELLYHealth to patients and audiologists including: reductions in hearing handicap, improved knowledge of hearing aid handling, use and communications strategies; and improved audiologist aftercare. The investigators will recruit 80 subjects (half in each group) and each subject will participate in the study for 8-12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02839759
Study type Interventional
Source Healthcare Technologies and Methods, LLC
Contact
Status Completed
Phase N/A
Start date August 31, 2018
Completion date April 30, 2020

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