NCT05909813

Brief Summary

The purpose of this study is to test the study method and procedure for individualized piano instruction (IPI) and its impact on chemotherapy related cognitive impairment (CRCI) symptoms. There have been studies that show the benefits of leaning to play the piano keyboard on cognitive skills in children and elderly populations. The information collected from the program will be used to examine the feasibility of implementing this program permanently

Trial Health

87
On Track

Trial Health Score

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

Enrollment
6

participants targeted

Target at below P25 for not_applicable breast-cancer

Timeline
Completed

Started Jan 2018

Shorter than P25 for not_applicable breast-cancer

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 8, 2018

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 4, 2018

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 29, 2018

Completed
4.9 years until next milestone

First Submitted

Initial submission to the registry

May 25, 2023

Completed
24 days until next milestone

First Posted

Study publicly available on registry

June 18, 2023

Completed
Last Updated

May 16, 2024

Status Verified

May 1, 2024

Enrollment Period

3 months

First QC Date

May 25, 2023

Last Update Submit

May 14, 2024

Conditions

Outcome Measures

Primary Outcomes (6)

  • Post-Individualized Piano Instruction Feasibility Questionnaire

    An investigator-designed questionnaire will be administered to participants, assessing their opinions about the program. The questionnaire includes multiple sections assessing participant session attendance, the effectiveness of the program, and how enjoyable it was. Total percentage scores will be calculated for each section. The Participants' attendance section scores range from "1" to "4" sessions. A higher number of sessions attended indicates greater perceived program feasibility. Questions assessing program effectiveness asked participants about their daily and weekly piano routines. Responses range from "not very easily" to "very easily". A higher positive response percentage indicates greater perceived program feasibility. Program enjoyment questions asked participants to rate their satisfaction. Responses range from "not enjoyable" to "very enjoyable".A higher positive response percentage indicates greater perceived program feasibility.

    Up to 8 weeks

  • Change in Cognition Scores: NIH Toolbox Cognition Battery

    The National Institutes of Health Toolbox Cognition Battery (NIHTB-CB) will be administered to participants to measure change in cognition after individualized piano instruction. The NIHTB-CB consists of tests of multiple constructs, yielding individual test scores and the following summary scores: Total Cognition Composite, Fluid Composite (includes Dimensional Change Card Sort, Flanker Inhibitory Control and Attention, Picture Sequence Memory (Form A), List Sorting Working Memory, and Pattern Comparison tests), and Crystallized Composite (includes Picture Vocabulary and Oral Reading Recognition tests). Scores on the NIHTB-CB will be used to assess severity of chemotherapy-related cognitive injury (CRCI) in participants. Scores range from 59-140, higher scores mean better cognition.

    Weeks 1, 4 and 8, Up to 8 weeks

  • Change in Quality of Life (QOL) Scores: Generalized Anxiety Disorder Assessment (GAD-7)

    The Generalized Anxiety Disorder Assessment (GAD-7) questionnaire will be administered to participants to measure the change in anxiety levels after individualized piano instruction. The GAD-7 consists of seven questions with each possible response scored on a four-point Likert scale ranging from "0" (not at all) to "4" (nearly every day). Higher total scores indicate greater severity of anxiety: 0-4 no to low-risk, 5-9 mild, 10-14 moderate, 15+ severe.

    Weeks 1, 4 and 8, Up to 8 weeks

  • Change in Quality of Life (QOL) Scores: Patient Health Questionnaire (PHQ-9)

    A Patient Health Questionnaire (PHQ-9) will be administered to participants to measure changes in mood after individualized piano instruction. The PHQ-9 consists of nine questions, with each possible response scored on a four-point Likert scale ranging from "0" (not at all) to "3" (nearly every day). Higher total scores indicate greater severity of depression: 0-4 none, 5-9 minimal, 10-14 moderate, 15-19 moderately severe, and 20-27 severe.

    Weeks 1, 4 and 8, Up to 8 weeks

  • Change in Cognition Scores: FACT-Cog

    The Functional Assessment of Cancer Therapy Cognitive Function (FACT-Cog) will be administered to participants to measure change in cognition after individualized piano instruction. The FACT-B is a 33-item questionnaire designed to assess perceived cognitive function and impact on quality of life in cancer patients within four domains: Perceived cognitive impairments, comments from others, perceiving cognitive abilities, and impact on quality of life. Each response within each domain is scored on a five-point Likert scale ranging from "0" (not at all) to 4 (very much). Higher total scores indicate a higher level of cognition and quality of life.

    Weeks 1, 4 and 8, Up to 8 weeks

  • Change in Quality of Life (QOL) Scores: FACT-B

    The Functional Assessment of Cancer Therapy-Breast (FACT-B) will be administered to participants to measure the change in the quality of life after individualized piano instruction (IPI). The FACT-B is a 36-item questionnaire designed to measure five domains of health-related QOL in breast cancer patients: Physical, social, emotional, and functional well-being as well as a breast-cancer subscale (BCS). Each response within each domain is scored on a five-point Likert scale ranging from "0" (not at all) to 4 (very much). Higher scores indicate a better quality of life.

    Weeks 1, 4 and 8, Up to 8 weeks

Study Arms (1)

Individualized Piano Instruction (IPI)

EXPERIMENTAL

Participants will receive six weeks of individualized piano instruction and two weeks follow-up for a total of eight weeks.

Behavioral: Individualized Piano Keyboard Instruction

Interventions

During weeks two through seven, participants will receive a once a week, hour long, in-person individualized piano keyboard instruction as follows: 1. Warm-up 1. Scales and Chords: Consisting of scales on seven major keys (C, D, E, F, G, A and B), chord progressions on I, IV, V, I. Two different keys will be learned every week. 2. 5-finger exercises will be completed four times per week. 2. Piano Theory and Music 1. Piano Theory: Playing through Alfred's Basic Adult All-in-One Course, Book 1, to be completed at the ability level of participant, with a least two new pages per lesson. 2. Chosen Piece: Playing through an instrumental piece chosen by the participant. Participants will be asked to practice homework from this lesson daily for 20 minutes per day, until their next weekly lesson.

Also known as: Individual Piano Instruction, IPI
Individualized Piano Instruction (IPI)

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients will be included into the study who:
  • Are over 18 years old
  • Speaks and read English
  • Have been diagnosed and treated for breast cancer (no specific etiology);
  • Are experiencing cognitive issues (i.e. actively complain to their physician about struggles with cognitive skills such as memory, attention, executive function, etc.);
  • Are 6 months or more out of active treatment;
  • Are not currently involved in other brain training programs.

You may not qualify if:

  • Adults who are diagnosed with a cognitive condition other than CRCI (Such as Alzheimer's, Parkinson's, dementia, Amyotrophic Lateral Sclerosis (ALS), autism, and cerebral palsy.)
  • Patients who are in active treatment for breast cancer (Currently hospitalized for chemotherapy or still visiting hospital for outpatient infusion treatment)
  • Adults who cannot read and write in English fluently.
  • Adults who do not have functional movements in their hands, as assessed by tendon gliding and finger opposition exercises provided by a physical hand therapist.
  • Adults who plan to not be in Miami for a period eight weeks or are unable to travel to Sylvester Miami on a weekly basis.
  • Adults who are already proficient in piano playing, music theory and play informally or professionally at least once per week.
  • Elderly adults, those older than 65 years old.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Miami

Miami, Florida, 33136, United States

Location

MeSH Terms

Conditions

Breast NeoplasmsChemotherapy-Related Cognitive Impairment

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesDrug-Related Side Effects and Adverse ReactionsChemically-Induced DisordersCognitive DysfunctionCognition DisordersNeurocognitive DisordersMental Disorders

Study Officials

  • Debbie Anglade, PhD, MSN, RN

    University of Miami

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Clinical

Study Record Dates

First Submitted

May 25, 2023

First Posted

June 18, 2023

Study Start

January 8, 2018

Primary Completion

April 4, 2018

Study Completion

June 29, 2018

Last Updated

May 16, 2024

Record last verified: 2024-05

Locations