A Study of Strengthening Teen Brain Resilience Using Music During Cancer Treatment

July 22, 2026 updated by: Mayo Clinic

Strengthening Teen Brain Resilience Using Music (STRUM) During Cancer Treatment: A Pilot Feasibility Trial

This clinical trial tests the feasibility and acceptability of the Strengthening Teen Brain Resilience Using Music (STRUM) intervention to improve radiation induced cognitive decline for adolescents undergoing radiation therapy for cancer treatment. Adolescents treated with radiation therapy for cancer often experience persistent cognitive deficits and reduced brain resilience or the ability to preserve cognitive and emotional functioning despite stressors. Musical instrument training has been shown to enhance memory, academic skills, and emotional well-being in youth. Although guitars are often the most preferred instrument, ukuleles offer greater accessibility due to their simplicity, affordability, and suitability for younger users. The STRUM intervention consists of virtual active music therapy ukulele lessons, which may be a feasible and acceptable way to improve radiation induced cognitive decline for adolescents undergoing radiation therapy for cancer treatment.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

30

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 Contact

Study Locations

    • Arizona
      • Scottsdale, Arizona, United States, 85259
        • Mayo Clinic in Arizona
        • Principal Investigator:
          • C. Robert Bennett, PhD, RN
        • Contact:
          • Robert Bennett, PhD, RN
          • Phone Number: 480-301-4394

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

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Aged 12-17 years at the time of enrollment
  • Receiving initial radiation therapy (RT) for cancer treatment with curative intent at the Mayo Clinic Arizona
  • Able to provide assent
  • Able to read and write in English
  • Have access to an electronic device with videoconferencing capability

Exclusion Criteria:

  • Less than three-month prognosis
  • Past history of RT
  • Self-reported visual, hearing, or cognitive impairment impeding the ability to complete the STRUM intervention
  • Prior receipt of ukulele or guitar lessons
  • Actively receiving musical instrument lessons

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: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Supportive care (STRUM sessions)
Patients receive a ukulele, tuner, and songbook and attend virtually delivered ukulele lessons over 30 minutes each, once weekly, for 10 weeks. Intervention sessions are structured with stair-stepping difficulty with each lesson concluding with learning a new song. Ten optional supplemental video-recorded lessons (approximately 15 minutes each) will be available for patients to view asynchronously and use for independent practice between weekly sessions. Patients are encouraged to practice their skills independently for at least 90 minutes per week. At the conclusion of the study, patients may attend an optional virtual "Encore Concert Event" remotely, featuring audio-video clips compiled from participants' lessons.
Ancillary studies
Ancillary studies
Attend STRUM sessions

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of eligible participants who consent to participate in this study (feasibility)
Time Frame: At time of enrollment
Feasibility defined as achieving a ≥ 70% consent rate among eligible participants.
At time of enrollment
Proportion of STRUM sessions completed (feasibility)
Time Frame: Up to 10 weeks
Participants will receive 10 weekly 30-minute virtual ukulele lessons over ten weeks. Basic descriptive statistical analyses will be performed.
Up to 10 weeks
Average weekly practice minutes
Time Frame: Up to 10 weeks
Assessed by patient self-report. Participants will be encouraged to practice their skills independently for at least 90 minutes per week. Basic descriptive statistical analyses will be performed.
Up to 10 weeks
Percentage of participants who complete ≥ 90% of the measures at each timepoint (feasibility)
Time Frame: Baseline, week 6, week 12, week 20
Basic descriptive statistical analyses will be performed.
Baseline, week 6, week 12, week 20
Acceptability of the Strengthening Teen Brain Resilience Using Music (STRUM) intervention
Time Frame: Approximately 2 weeks following end of intervention (week 12)
Defined as mean Acceptability of Intervention Measure (AIM) score of ≥ 3/4, supported by exit interview feedback. Basic descriptive statistical analyses will be performed. The AIM is a study-specific measure that consists of 4 questions, each answered on a scale of 1 (completely disagree) to 5 (completely agree). Higher scores indicate greater acceptability.
Approximately 2 weeks following end of intervention (week 12)
Participant perspective on meaningfulness of the STRUM intervention
Time Frame: Approximately 2 weeks following end of intervention (week 12)
Assessed by exit interview feedback. Participants will complete semi-structured exit interviews (approximately 30-minute duration). Exit interview transcripts will be analyzed and coded using thematic analyses. Thematic findings will be used to refine the intervention design and delivery.
Approximately 2 weeks following end of intervention (week 12)
Change in brain resilience
Time Frame: Baseline, week 6, week 12, week 20
Assessed by cognitive testing using the BrainCheck Assess™ digital platform. Each testing session should take approximately 15 minutes. Standard aggregate scores range from 0-200 with lower scores generally suggesting greater cognitive impairment.
Baseline, week 6, week 12, week 20

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: C. Robert Bennett, PhD, RN, Mayo Clinic

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 (Estimated)

October 1, 2026

Primary Completion (Estimated)

November 1, 2028

Study Completion (Estimated)

November 1, 2028

Study Registration Dates

First Submitted

July 22, 2026

First Submitted That Met QC Criteria

July 22, 2026

First Posted (Actual)

July 27, 2026

Study Record Updates

Last Update Posted (Actual)

July 27, 2026

Last Update Submitted That Met QC Criteria

July 22, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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