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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03112850




Registration number
NCT03112850
Ethics application status
Date submitted
1/04/2017
Date registered
13/04/2017

Titles & IDs
Public title
Cognition Effects of Hearing Aids and Auditory Training in Older Age
Scientific title
Investigating the Impact of Hearing Aid Use and Auditory Training on Cognition, Mood and Social Interaction in Older Adults With Hearing Loss
Secondary ID [1] 0 0
SHR Project 2016/159
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hearing Loss, Sensorineural 0 0
Condition category
Condition code
Ear 0 0 0 0
Deafness

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - Hearing aid

Active comparator: Group A - Participants who will be fitted with hearing aids for the first 3 months of 6 months auditory training program

Active comparator: Group B - Participants who will be fitted with hearing aids for the second 3 months of 6 months auditory training program


Treatment: Devices: Hearing aid
LOF hearing aid

Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change over six months in SUCCAB performance (accuracy/reaction time) measures
Timepoint [1] 0 0
Change from baseline to six months
Secondary outcome [1] 0 0
Change in the Geriatric Depression Scale (GDS) aggregated into a single score
Timepoint [1] 0 0
Change from baseline to six months
Secondary outcome [2] 0 0
The Berkman-Syme Social Network Index aggregated into a single score
Timepoint [2] 0 0
Change from baseline to six months

Eligibility
Key inclusion criteria
1. Be aged between 50 and 90 years
2. Have good working knowledge of English
3. Mild or moderate symmetric sensorineural hearing loss with a pure-tone average (PTA) of thresholds at 0.5 - 6 kHz in both ears
4. Willing to wear hearing aids for three (3) months
5. Willing to undergo weekly auditory training for a period of six (6) months.
6. Submit written consent to participant in study
Minimum age
50 Years
Maximum age
90 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Any significant visual impairment that would prevent them from reading or performing computer based tasks.
2. Suspected cognitive impairment (defined as a score less or equal to 24 on the MMSE)
3. Severe or profound hearing loss

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Swinburne University of Technology - Melbourne
Recruitment postcode(s) [1] 0 0
3122 - Melbourne

Funding & Sponsors
Primary sponsor type
Other
Name
Swinburne University of Technology
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Denny Meyer, PhD
Address 0 0
Swinburne University of Technology
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
No/undecided IPD sharing reason/comment
There is no plan


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.