Feasibility of Virtual, Tailored, Music-Based Relaxation for Anxiety in Adolescent and Young Adult Cancer Survivors

Completed · Not applicable

Conditions studied: Anxiety

In brief

Demonstrate the feasibility of conducting an eight-week, (45 min/week), theory driven, virtually-delivered, tailored music-based relaxation (TiMBRe) intervention to decrease anxiety in adolescent and young adult (AYA) cancer survivors with clinically-relevant anxiety.

Key facts

Study ID

NCT05911269

Run by

University of Michigan Rogel Cancer Center

People needed

50

Starts

2025-01-21

Expected to finish

2026-07-24

Last updated by the study team

2026-07-28

Who can join

Age: 15 and older, up to 39. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 15 - 39 years old
• at least one month post cancer treatment
• report clinically relevant anxiety in the past seven days (PROMIS Anxiety 4a scores ≥ 55)35
• speak/read English.

You may not qualify if…

• prognosis less than 3 months
• documentation of significant hearing impairment
• plan to receive surgery, radiation, or chemotherapy for cancer treatment during the study period
• plans in place to begin new psychosocial (i.e., cognitive behavioral therapy14 or mindfulness-based stress reduction15) or pharmacological treatments for anxiety during the study. Although, participants may continue psychosocial or pharmacological treatments for anxiety if the treatments were initiated at least eight weeks prior to study enrollment, the dose has not changed, and they report clinically relevant anxiety in the last week.

Where it is running

• University of Michigan — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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