NCT07772765

Brief Summary

The proposed study will enroll healthy older adult participants to examine the effectiveness of music listening activities to promote hearing and cognition. Participants will be randomized into one of four experimental groups and can expect to participate for up to 21 hours of research distributed over 20 weeks.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
216

participants targeted

Target at P75+ for not_applicable

Timeline
11mo left

Started Oct 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 14, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 19, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

October 19, 2026

Expected
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2027

3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2027

Last Updated

September 30, 2026

Status Verified

August 1, 2026

Enrollment Period

7 months

First QC Date

August 14, 2026

Last Update Submit

September 29, 2026

Conditions

Keywords

Cognitive TrainingAuditory TrainingMusicAging

Outcome Measures

Primary Outcomes (3)

  • Digits-in-Noise Task

    The Digits-in-Noise (DIN) test presents trials of three sequential spoken digits against a broad-band, speech-shaped masker. Signal/noise ratio is varied adaptively to track 50% correct. The dependent variable is the threshold noise tolerance in dB. Lower scores indicate better performance.

    Pre-test (week 1), Mid-test (week 5), Post-test (week 10), Follow-up (week 18)

  • Spatial Release From Masking Task

    Tests the ability to distinguish speech from competing speech. Collocated condition uses target and two competing maskers all located directly in front of the listener, and spatially separated condition uses two masking sentences sent from 45 degrees to the left and right of center. Sentences are correctly identified as part of a series of test trials in which TMR progressively reduced every two trials. The dependent variable is the threshold target-to-masker ratio (TMR) as estimated based on the number of sentences correctly identified. Lower scores indicate better performance.

    Pre-test (week 1), Mid-test (week 5), Post-test (week 10), Follow-up (week 18)

  • Dichotic Sentence Identification Task

    The DSI test simultaneously presents two nonsense sentences, one to each ear. Participants indicate two sentences heard from a list of alternatives. DSI sentences are presented at a comfortable listening level, usually 50 dB above pure-tone average of each ear. The dependent variable is the percentage of sentences correctly identified. Higher scores indicate better performance.

    Pre-test (week 1), Mid-test (week 5), Post-test (week 10), Follow-up (week 18)

Secondary Outcomes (9)

  • Revised Hearing Handicap Inventory for the Elderly (RHHI)

    Pre-test (week 1), Post-test (week 10), Follow-up (week 18)

  • Speech Recognition Threshold using Coordinate Response Measure

    Pre-test (week 1), Mid-test (week 5), Post-test (week 10), Follow-up (week 18)

  • Gap Detection Task

    Pre-test (week 1), Post-test (week 10)

  • Spectrotemporal Sensitivity Task

    Pre-test (week 1), Post-test (week 10)

  • Monaural and Binaural Sensitivity to Frequency Modulation Task

    Pre-test (week 1), Post-test (week 10)

  • +4 more secondary outcomes

Other Outcomes (6)

  • POMS 2-A

    Pre-test (week 1), Post-test (week 10), Follow-up (week 18)

  • Ryff's Scale of Psychological Well-being Score

    Pre-test (week 1), Follow-up (week 18), Follow-up (week 18)

  • Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS)

    Pre-test (week 1), Follow-up (week 18), Follow-up (week 18)

  • +3 more other outcomes

Study Arms (4)

Sound of Music Plus Attention

EXPERIMENTAL
Behavioral: Music Listening with Attentional prompts

Sound of Music

EXPERIMENTAL
Behavioral: Music Listening

Sound of Tones Plus Attention

EXPERIMENTAL
Behavioral: Tone listening with Attentional prompts

Business as usual Control

NO INTERVENTION

Interventions

Participants will listen to musical excerpts, and guided instructions will be provided to tell the participants what aspect of the music to pay attention to and how to respond. Participants will log responses on an interactive tablet-based interface.

Sound of Music Plus Attention
Music ListeningBEHAVIORAL

Participants will listen to musical excerpts and will be provided with guided instructions directing their attention to specific aspects of the music. Participants will report when they perceive a noticeable change in the music (e.g., changes in instrumentation, rhythm, texture, or intensity). Participants will log responses on an interactive tablet-based interface.

Sound of Music

Participants will be asked to attend to auditory stimuli and respond to them according to guided instructions. Participants will log responses on an interactive tablet-based interface.

Sound of Tones Plus Attention

Eligibility Criteria

Age60 Years - 101 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age: 60+
  • No self-reported auditory difficulties and normal or near-normal hearing sensitivity as measured by SRTs.
  • Should have no more than typical hearing loss for their age and no evidence of dementia.
  • Fluent in English and/or Spanish
  • No more than two years of formal music training in childhood OR in the past 20 years

You may not qualify if:

  • Abnormal vision or hearing prohibitive of training
  • History of seizures, focal brain lesion, or head injury with loss of consciousness
  • Physical handicap (motor or perceptual) that would impede training procedures
  • Social, educational or economic hardship prohibitive to training schedule Concurrent enrollment in other cognitive training studies
  • History of major psychiatric illness, including psychosis, bipolar disorder, depression, alcohol or substance abuse, recent bereavement
  • Geriatric Depression Scale-15 (GDS-15) score of 6 or higher, indicating clinically significant depressive symptoms
  • Not being proficient enough in English or Spanish that would prevent following and understanding all instructions and completing all testing sessions
  • Diagnosis of dementia or other neurological disease, including mild cognitive impairment (MCI)
  • Telephone-Montreal Cognitive Assessment (t-MoCA) score of 16 or less

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northeastern University

Boston, Massachusetts, 02115, United States

RECRUITING

Study Officials

  • Susanne Jaeggi, PhD

    Northeastern University

    PRINCIPAL INVESTIGATOR
  • Aaron Seitz, PhD

    Northeastern University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Psychology, Applied Psychology, Music

Study Record Dates

First Submitted

August 14, 2026

First Posted

August 19, 2026

Study Start (Estimated)

October 19, 2026

Primary Completion (Estimated)

May 31, 2027

Study Completion (Estimated)

August 31, 2027

Last Updated

September 30, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will share

All individual participant data (anonymized)

Shared Documents
SAP, ICF
Time Frame
Data will be available persistently at the conclusion of the study.
Access Criteria
There are no access criteria.

Locations