Actively Recruiting
Benefits of Choir for Older Adults With Unaddressed Hearing Loss (WP2)
Led by Toronto Metropolitan University · Updated on 2025-09-18
210
Participants Needed
7
Research Sites
72 weeks
Total Duration
On this page
Sponsors
T
Toronto Metropolitan University
Lead Sponsor
M
Memorial University of Newfoundland
Collaborating Sponsor
AI-Summary
What this Trial Is About
Unaddressed age-related hearing loss is highly prevalent among older adults, typified by negative consequences for speech-in-noise perception and psychosocial wellbeing. There is promising evidence that group singing may enhance speech-in-noise perception and psychosocial wellbeing. However, there is a lack of robust evidence, primarily due to the literature being based on small sample sizes, single site studies, and a lack of randomized controlled trials. Hence, to address these concerns, this SingWell Project study utilizes an appropriate sample size, multisite, randomized controlled trial approach, with a robust preplanned statistical analysis. The objective of the study is to explore if group singing may improve speech-in-noise perception and psychosocial wellbeing for older adults with unaddressed hearing loss. The investigators designed an international, multisite, randomized controlled trial to explore the benefits of group singing for adults aged 60 years and older with unaddressed hearing loss. After undergoing an eligibility screening process and completing an information and consent form, the investigators intend to recruit 210 participants that will be randomly assigned to either group singing or an audiobook club (control group) intervention for a training period of 12-weeks. The study has multiple timepoints for testing, that are broadly categorized as macro (i.e., pre- and post-measures across the 12-weeks), or micro timepoints (i.e., pre- and post-measures across a weekly training session). Macro measures include behavioural measures of speech and music perception, and psychosocial questionnaires. Micro measures include psychosocial questionnaires and heart-rate variability. The investigators hypothesize that group singing may be effective at improving speech perception and psychosocial outcomes for older adults with unaddressed hearing loss-more so than participants in the control group.
CONDITIONS
Official Title
Benefits of Choir for Older Adults With Unaddressed Hearing Loss (WP2)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 60 years and older
- Bilateral mild-to-moderate hearing loss (20-49 dB hearing level) measured by four-frequency pure-tone average at 500 Hz, 1000 Hz, 2000 Hz, and 4000 Hz
- Unaddressed hearing loss (no current use of hearing aids, cochlear implants, or assistive listening devices)
- No significant cognitive impairment with a Montreal Cognitive Assessment for hearing impairment (MoCA-H) score of 24 or higher
- Do not use a pacemaker or anti-arrhythmic medications
- Not currently involved in regular active music learning or audiobook clubs within the last year
- Sufficient language ability to understand and complete test materials in English, Dutch, or German depending on the study site
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 7 locations
1
Brain and Creativity Institute, University of Southern California
Los Angeles, California, United States, 90089
Not Yet Recruiting
2
Flinders University
Adelaide, South Australia, Australia, 5042
Not Yet Recruiting
3
Memorial University of Newfoundland
St. John's, Newfoundland and Labrador, Canada, A1C 5S7
Not Yet Recruiting
4
Toronto Metropolitan University
Toronto, Ontario, Canada, M5B 2K3
Actively Recruiting
5
Concordia University
Montreal, Quebec, Canada, H3G 1M8
Not Yet Recruiting
6
Carl von Ossietzky Universitat Oldenburg
Oldenburg, Germany, D-26129
Not Yet Recruiting
7
University of Groningen
Groningen, Netherlands, 9700 AB
Actively Recruiting
Research Team
C
Chi Yhun Lo, PhD
CONTACT
K
Kay F Wright-Whyte, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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