The Impact of Piano Training on Cognitive Performance and Psychosocial Well-Being in Older Adults

April 29, 2019 updated by: Jennifer Bugos, University of South Florida
This project evaluates the effects of piano training and computerized cognitive training on cognitive performance in healthy older adults compared to controls. The project is intended for healthy older adults (60-80 years) with little to no previous musical training (less than three years of prior musical training or cognitive training and not currently engaged in music reading or musical performance, less than 10 hours of previous cognitive training). Investigators anticipate that musical engagement will serve as an enjoyable cognitive intervention for older adults. Investigators believe that piano training will enhance cognitive performance on executive functions essential for maintaining independence in older adulthood. Learning a musical instrument, while challenging, will improve self-efficacy, mood, and qualtiy of life. Participants engaged in piano training will demonstrate reduced cortisol levels and increased immune function responses. Investigators predict that adults enrolled in computerized cognitive training will demonstrate enhanced memory, working memory and self-efficacy post-training.

Study Overview

Status

Completed

Conditions

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

Interventional

Enrollment (Actual)

93

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Tampa, Florida, United States, 33620
        • University of South Florida

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
The intervention focuses upon progressively difficult piano performance exercises (repertoire), technique, and finger dexterity exercises.
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.
No Intervention: A 3 No Treatment Controls
No classes will be provided to our control group. This is a no-treatment control group.

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
(CHANGE) up to 16 weeks and after study completion 7 months
Trail Making Test
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
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
Motor Speed
(CHANGE) up to 16 weeks and after study completion 7 months
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
(CHANGE) up to 16 weeks and after study completion 7 months
Musical Performance Self-Efficacy
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
Musical Self-Efficacy
(CHANGE) up to 16 weeks and after study completion 7 months
General Self-Efficacy
Time Frame: (CHANGE) up to 16 weeks and after study completion 7 months
General Self-Efficacy
(CHANGE) up to 16 weeks and after study completion 7 months
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jennifer Bugos, PhD, Assistant Professor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2015

Primary Completion (Actual)

June 1, 2017

Study Completion (Actual)

June 1, 2017

Study Registration Dates

First Submitted

September 16, 2015

First Submitted That Met QC Criteria

September 28, 2015

First Posted (Estimate)

October 1, 2015

Study Record Updates

Last Update Posted (Actual)

May 1, 2019

Last Update Submitted That Met QC Criteria

April 29, 2019

Last Verified

April 1, 2019

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)?

NO

IPD Plan Description

No, there is no plan to share individual participant data. We plan on publishing all data collectively.

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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