- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03999606
Short-Term Music Training and Auditory Processing in Older Adults
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Los Angeles, California, United States, 90089
- Brain and Creativity Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Native English speaker with experience of subjective hearing loss;
- Normal IQs (standard score of >85) as measured by the two-subtest Abbreviated Wechsler's Adult Scale of Intelligence.
Exclusion Criteria:
- Use of prescribed hearing aids;
- Sever hearing loss (thresholds of 60 and 95 dB)
- Current diagnosis of neurological or psychiatric disorders
- Impaired cognitive function (all participants will be screened with the Montreal Cognitive Assessment Battery)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Mindfulness Training
Participants in the control group will be assigned to a online based mindfulness training.
|
Sixty participants, ages 50-65, will be recruited to partake in this study and will be randomly assigned to two groups: participants in the experimental group will join a weekly on-line choir via Zoom, for ten weeks, directed by a professionally trained conductor from USC Department of Choral Music. The group practice will be accompanied by individual singing lessons (online or CDs) for home practice. Participants in the control group will be provided with weekly remote mindfulness lessons also on an online platform. |
Experimental: Music Training
Participants in the experimental group will be assigned to a online based choir program.
|
Sixty participants, ages 50-65, will be recruited to partake in this study and will be randomly assigned to two groups: participants in the experimental group will join a weekly on-line choir via Zoom, for ten weeks, directed by a professionally trained conductor from USC Department of Choral Music. The group practice will be accompanied by individual singing lessons (online or CDs) for home practice. Participants in the control group will be provided with weekly remote mindfulness lessons also on an online platform. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Enhanced speech in noise perception
Time Frame: 15 weeks
|
The effects of age on participants' ability to detect speech in noise will be assessed using the QuickSIN test (Speech-In-Noise; Version 1.3).
|
15 weeks
|
Enhanced speech in noise perception
Time Frame: 15 weeks
|
EEG data will be collected using the speech syllable /da/, spoken in isolation by an American female.
The stimulus will be presented in four conditions, in quiet and in presence of an 8-talker babble noise at three SNRs (10, 5 and 0 dB), presented in a random order for each participant, with an inter-stimulus interval of 1000 ms.
|
15 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Psychological Well-Being
Time Frame: 15 weeks
|
Ryff's Psychological Well-Being Scale (2007) will be used to measure six aspects of wellbeing and happiness including autonomy, environmental mastery, personal growth, positive relations, purpose in life, and self-acceptance
|
15 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- UP-19-00350
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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