Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12617001616369
Ethics application status
Approved
Date submitted
22/11/2017
Date registered
11/12/2017
Date last updated
25/06/2021
Date data sharing statement initially provided
21/01/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
This research study will use Magnetic Resonance Imaging (MRI) techniques to learn whether hearing aids do have an effect on cognitive function and the brain of older adults with hearing loss.
Scientific title
Using Magnetic Resonance Imaging to Investigate the Effects of Hearing Aid Use on Brain Activity and Cognitive Function in Older Adults with Sensorineural Hearing Loss.
Secondary ID [1] 293394 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hearing loss 305539 0
Cognitive decline 305540 0
Depression 305541 0
Condition category
Condition code
Ear 304771 304771 0 0
Deafness
Mental Health 304772 304772 0 0
Studies of normal psychology, cognitive function and behaviour
Mental Health 304773 304773 0 0
Depression

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
First-time hearing aid users will wear a pair of hearing aids for six (6) months to address their hearing loss. These are MoxiFit Flex trial hearing aids supplied by Unitron which will be worn by participants at all convenient times (except when asleep or in water). Practice of lipreading is not part of the intervention but it is expected to occur in response to hearing loss. Therefore, a simple lipreading test will be conducted before each MRI scan.
Only a random sample of first time hearing aid users will have extensive MRI scanning at baseline (i.e. before hearing aid fitting) and at six months (i.e. after using hearing aids for a period of six months).
Intervention code [1] 299642 0
Treatment: Devices
Comparator / control treatment
Long-term hearing aid users, with at least one year hearing aid use experience, will continue to wear their hearing aids for the study period (six (6) months).
Control group
Active

Outcomes
Primary outcome [1] 303994 0
The Incongruent Stroop cognitive performance task using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB) measures is primary outcome [1]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [1] 303994 0
Six months after baseline assessments
Secondary outcome [1] 340674 0
Depression, Anxiety and Stress (DASS) composite score.
Timepoint [1] 340674 0
From baseline to six months.
Secondary outcome [2] 340675 0
The Berkman-Syme Social Network Index aggregated into a single score
Timepoint [2] 340675 0
From baseline to six months
Secondary outcome [3] 340733 0
Pure Tone Audiometric (PTA) hearing measure
Timepoint [3] 340733 0
Baseline to 6 months
Secondary outcome [4] 341000 0
Lipreading Ability Test
Timepoint [4] 341000 0
Baseline to 6 months
Secondary outcome [5] 365929 0
Brain activity which will be measured using MRI technology (SPM12 - Wellcome Department of Neurology) for a random sample of first-time hearing aid users.
Timepoint [5] 365929 0
Baseline to 6 months
Secondary outcome [6] 365930 0
The Simple Reaction Time cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [6]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [6] 365930 0
Baseline to 6 months
Secondary outcome [7] 365931 0
The Complex Reaction Time cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [7]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [7] 365931 0
Baseline to 6 months
Secondary outcome [8] 365932 0
The Immediate Recognition Memory cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [8]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [8] 365932 0
Baseline to 6 months
Secondary outcome [9] 365933 0
The Delayed Recognition Memory cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [9]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [9] 365933 0
Baseline to 6 months
Secondary outcome [10] 365934 0
The Spatial Working Memory cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [10]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [10] 365934 0
Baseline to 6 months
Secondary outcome [11] 365935 0
The Contextual Recognition Memory cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [11]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [11] 365935 0
Baseline to 6 months
Secondary outcome [12] 365936 0
The Congruent Stroop cognitive performance task, assessed using Swinburne University Computerised Cognitive Assessment Battery (SUCCAB), is secondary outcome measure [12]. This outcome will be measured at baseline and at six months, after hearing aid intervention.
Timepoint [12] 365936 0
Baseline to 6 months

Eligibility
Key inclusion criteria
1) 55 to 90 years
2) A good working knowledge of English
3) Mild or moderate sensorineural hearing loss with a pure-tone average (PTA) of thresholds at 0.5 – 6 kHz in both ears
4) Willing to undergo two (2) one hour MRI scans over a period of 6 months
5) Willing to wear hearing aids for six (6) months
6) Must have been wearing hearing aids for at least one (1) year (only for people with hearing aid experience)
7) Written consent to participate in the study
Minimum age
55 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 reading
2) Suspected cognitive impairment (defined as a score less than or equal to 23 on the MMSE)
3) Severe or profound hearing loss
4) Any person suffering from claustrophobia
5) Any person with a pacemaker, metal clips or arteries or certain implanted devices
6) Any left-handed person

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



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Methods:
No previous studies exist to determine what effect sizes can be expected for this study. This is only a pilot study which will provide initial estimates for the relevant means, standard deviations and effect sizes.

Chi-squared and MANOVA analyses will be used to compare the groups in terms of demographics and baseline outcome measures. Mixed Model Repeated Measures analyses will be conducted to test for significant differences between the groups in terms of changes that occur in the outcome measures from baseline to 6 months.

Recruitment
Recruitment status
Stopped early
Data analysis
No data analysis planned
Reason for early stopping/withdrawal
Lack of funding/staff/facilities
Other reasons/comments
Other reasons
Study has stopped early due to changes in MRI requirements
Date of first participant enrolment
Anticipated
11/12/2017
Actual
8/01/2018
Date of last participant enrolment
Anticipated
Actual
31/10/2018
Date of last data collection
Anticipated
31/07/2019
Actual
Sample size
Target
60
Accrual to date
Final
25
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment postcode(s) [1] 18133 0
3132 - Mitcham
Recruitment postcode(s) [2] 18134 0
3122 - Hawthorn

Funding & Sponsors
Funding source category [1] 298020 0
University
Name [1] 298020 0
Swinburne University of Technology
Country [1] 298020 0
Australia
Primary sponsor type
Individual
Name
Professor Denny Meyer
Address
Centre for Mental Health
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Country
Australia
Secondary sponsor category [1] 297093 0
Individual
Name [1] 297093 0
Ms. Joanna Nkyekyer
Address [1] 297093 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Country [1] 297093 0
Australia
Secondary sponsor category [2] 297098 0
Individual
Name [2] 297098 0
Dr. Matthew Hughes
Address [2] 297098 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Country [2] 297098 0
Australia
Secondary sponsor category [3] 297099 0
Individual
Name [3] 297099 0
Associate Professor Andrew Pipingas
Address [3] 297099 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Country [3] 297099 0
Australia
Secondary sponsor category [4] 297100 0
Individual
Name [4] 297100 0
Associate Professor Sunil Bhar
Address [4] 297100 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Country [4] 297100 0
Australia
Other collaborator category [1] 279820 0
Individual
Name [1] 279820 0
Ms. Alison Hennessy
Address [1] 279820 0
Alison Hennessy Audiology,
444 Mitcham Road,
Mitcham Vic 3132
Country [1] 279820 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 299055 0
Swinburne's Human Research Ethics Committee (SUHREC)
Ethics committee address [1] 299055 0
Ethics committee country [1] 299055 0
Australia
Date submitted for ethics approval [1] 299055 0
22/09/2017
Approval date [1] 299055 0
18/11/2017
Ethics approval number [1] 299055 0
SHR Project 2017/266

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

Contacts
Principal investigator
Name 79130 0
Prof Denny Meyer
Address 79130 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Melbourne - Australia
Country 79130 0
Australia
Phone 79130 0
+61 3 92144824
Fax 79130 0
Email 79130 0
[email protected]
Contact person for public queries
Name 79131 0
Joanna Nkyekyer
Address 79131 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Melbourne - Australia
Country 79131 0
Australia
Phone 79131 0
+61 4 22733157
Fax 79131 0
Email 79131 0
[email protected]
Contact person for scientific queries
Name 79132 0
Denny Meyer
Address 79132 0
Swinburne University of Technology
John Street, Hawthorn Vic 3122
Melbourne - Australia
Country 79132 0
Australia
Phone 79132 0
+61 4 22733157
Fax 79132 0
Email 79132 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
Summarized data will be made available in publications.


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
1068Study protocol    Hughes ME, Nkyekyer J, Innes-Brown H, Rossell SL, ... [More Details]



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.