- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02564601
The Impact of Piano Training on Cognitive Performance and Psychosocial Well-Being in Older Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The project purpose is to scientifically examine the benefits of piano training as compared to computer cognitive training and no treatment controls on cognitive (processing speed, task-switching, verbal fluency, verbal memory, and working memory), psychosocial (mood, self-efficacy, and quality of life), and physiological variables (biomarkers) in healthy older adult participants in a randomized clinical trial design.
Participants: Ninety community dwelling older adults will be recruited from the community. Criteria for enrollment are: between the ages of 60-80, native English speakers, not currently taking medications affecting memory performance, have no pre-existing cognitive impairment or neurological disorders, (as indicated by the Telephone Interview for Cognitive Status > 30), no moderate to severe depression (as indicated by the Geriatric Depression Scale), no difficulty with hand movements, less than three years of prior musical training, not currently engaged in music reading or musical performance, and less than ten hours of prior computer brain training experience. Participants will be randomly assigned to one of three groups stratified by intelligence and gender: piano instruction, computerized cognitive training or a no treatment control group. Informed written consent will be obtained in accordance with the Institutional Review Board.
Procedure: Participants will be tested in three visits: pre-training, immediately post-training, and three months follow-up. Those randomized to piano training or computerized cognitive training will complete their assigned training between pre-training and post-training visits. Measures of music aptitude and intelligence will be administered at the pre-training visit. These factors can influence cognitive performance. Any significant differences at baseline between the three assigned groups will be statistically controlled for in the analyses. Standardized cognitive measures will be used to examine processing speed, task-switching, verbal fluency, verbal memory, and working memory at each visit. Psychosocial outcomes (mood, self-efficacy, and quality of life) and physiological biomarkers will also be evaluated at each visit.
The goal for both interventions will be to complete 48 hours of group training over a four month period (16 weeks). Sixty participants (30 piano training; 30 auditory computer training) will be asked to attend three hours of training each week. Thirty participants will serve in the no treatment control group. Piano training will consist of basic piano technique, dexterity exercises, piano literature, and music theory. Participants will be expected to perform all major scales, repertoire from the Alfred All-in-One Method, and complete weekly theory assignments. Each class session is structured as a cognitive intervention that focuses upon review of materials (15-20 min), and the remaining portion of the class focuses upon learning new skills and concepts. Computerized cognitive training involves computerized perceptual practice exercises that vary in difficulty ranging from basic auditory processing speed to application through memory exercises. Within each exercise, the stimuli (i.e., tones, speech sounds, words, sentences) become less discriminable and speed of presentation increases (making the exercises more difficult) as performance improves. The Brain Fitness training program with working memory exercises will be used.
Data source(s). Data will consist of a series of standardized cognitive, psychosocial, and neurophysiological measures administered at three time points: pre-training, post-training, and at a three month follow-up. All standardized measures have been previously used to assess the efficacy of cognitive training approaches and demonstrate good psychometric properties.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Florida
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Tampa, Florida, United States, 33620
- University of South Florida
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Between the ages of 60-80
- native English speakers
- no pre-existing cognitive impairment or neurological impairment
- not taking medications affecting memory performance (sleep meds, antidepressants, etc.)
- Telephone Interview for Cognitive Status (score >30)
- no moderate to severe depression
- no difficulty with hand movements
- less than three years of formal music training
- no difficulty with the movement of their hands
- not currently engaged in music reading or musical performance
- < 10 hours of previous cognitive training
Exclusion Criteria:
- Those not between 60-80
- those taking medications affecting memory performance
- Non-Native English Speakers
- Those with pre-existing cognitive impairment
- Telephone Interview for Cognitive Status (score < 30)
- Those with difficulty in the movement of their hands
- Those with more than three years of formal music training or currently engaged in music reading or music performance
- Those with more than ten hours of cognitive training
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: A1 Piano Training
16 weekly classes will be provided to the piano training group.
Each piano class session will focus upon review of materials (15-20 min), and the remaining portion of the class will focus upon learning new skills and concepts.
This course includes finger dexterity exercises, basic piano technique, and basic piano repertoire.
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The intervention focuses upon progressively difficult piano performance exercises (repertoire), technique, and finger dexterity exercises.
|
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Experimental: A2 Computer Cognitive Training
16 weekly classes will be provided to the computerized cognitive training group.
Computerized cognitive training involves process-based computerized practice of adaptive perceptual exercises.
Each computer cognitive training class session will focus upon practice of cognitive exercises that vary in difficulty ranging from basic auditory processing speed to application through memory and working memory exercises.
Within each exercise, the stimuli (i.e., tones, speech sounds, words, sentences) become less discriminable and speed of presentation increases (making the exercises more difficult) as performance improves.
|
The intervention focuses upon progressively difficult perceptual exercises using the Brain Fitness program plus working memory exercises.
|
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No Intervention: A 3 No Treatment Controls
No classes will be provided to our control group.
This is a no-treatment control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
N-Back
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Working Memory Measure in the Visual Domain
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Cued Color Word Stroop
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Cognitive Control, Inhibition
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Digit Coding- WAIS IV subtest
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Simple Processing Speed
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Symbol Search- WAIS IV subtest
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Visual Scanning
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Paced Auditory Serial Addition Task (PASAT)
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Complex processing speed
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Rey Auditory Verbal Learning Test
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Verbal Memory
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Delis Kaplan Executive Function Verbal Fluency subtest
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Category Fluency, Letter Fluency, Category Switching
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(CHANGE) up to 16 weeks and after study completion 7 months
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|
Trail Making Test
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
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Planning and Processing Speed
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
Finger Tapper Test
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
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Motor Speed
|
(CHANGE) up to 16 weeks and after study completion 7 months
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|
Salivary Cortisol
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Stress Levels
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
|
SIgA levels
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Immune Function
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(CHANGE) up to 16 weeks and after study completion 7 months
|
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Musical Performance Self-Efficacy
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
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Musical Self-Efficacy
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(CHANGE) up to 16 weeks and after study completion 7 months
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General Self-Efficacy
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
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General Self-Efficacy
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(CHANGE) up to 16 weeks and after study completion 7 months
|
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Cognitive Self-Report Questionnaire (25)
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
|
Mood
|
(CHANGE) up to 16 weeks and after study completion 7 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jennifer Bugos, PhD, Assistant Professor
Publications and helpful links
General Publications
- Smith GE, Housen P, Yaffe K, Ruff R, Kennison RF, Mahncke HW, Zelinski EM. A cognitive training program based on principles of brain plasticity: results from the Improvement in Memory with Plasticity-based Adaptive Cognitive Training (IMPACT) study. J Am Geriatr Soc. 2009 Apr;57(4):594-603. doi: 10.1111/j.1532-5415.2008.02167.x. Epub 2009 Feb 9.
- Duff K, Tometich D, Dennett K. The Modified Telephone Interview for Cognitive Status is More Predictive of Memory Abilities Than the Mini-Mental State Examination. J Geriatr Psychiatry Neurol. 2015 Sep;28(3):193-7. doi: 10.1177/0891988715573532. Epub 2015 Feb 26.
- Bugos JA, Perlstein WM, McCrae CS, Brophy TS, Bedenbaugh PH. Individualized piano instruction enhances executive functioning and working memory in older adults. Aging Ment Health. 2007 Jul;11(4):464-71. doi: 10.1080/13607860601086504.
- Bugos JA, Wang Y. Piano Training Enhances Executive Functions and Psychosocial Outcomes in Aging: Results of a Randomized Controlled Trial. J Gerontol B Psychol Sci Soc Sci. 2022 Sep 1;77(9):1625-1636. doi: 10.1093/geronb/gbac021.
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 (Estimate)
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
- 19415
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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