ClinicalTrials.gg
Not yet recruitingNCT07653360Updated Oct 15, 2026

Music Therapy for Oral Mucositis Pain in Pediatric Patients

An interventional study of Semi-Structured Interviews in Oral Mucosa Discomfort, Pediatric Cancer and Mucositis Oral, sponsored by University of California, San Francisco. Not yet recruiting at 1 site in United States. Open to participants aged 6 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-15.

Sponsored by University of California, San Francisco · Not applicable, Interventional, and Supportive care

Updated Oct 15, 2026Start date movedPrimary completion moved+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
6 Years to 64 Years
Sex
All
01

Study summary

This mixed-methods pilot study will examine the effect of music therapy on oral mucositis pain in pediatric oncology patients. Oral mucositis, characterized by painful ulcerative lesions in the mouth, is a common side effect of high-dose chemotherapy and hematopoietic stem cell or bone marrow transplantation. Despite its high prevalence and impact on quality of life, effective pain management strategies for pediatric oral mucositis remain limited and often rely heavily on medications that may cause significant side effects or provide insufficient relief. Music therapy may offer a promising non-pharmacologic adjunct for reducing pain, yet no studies to date have specifically evaluated its use for oral mucositis pain in pediatric patients.

Read the detailed description

Phase 1:

Aim 1a: Explore the experiences of oral mucositis pain in pediatric patients.

Aim 1b: Explore how pediatric patients perceive the involvement of music therapy during oral mucositis pain.

Phase 1 of the study involves semi-structured interviews with parent-child dyads about the child's experiences with oral mucositis and their perceptions of music therapy while experiencing oral mucositis pain. Information obtained in Phase 1 will direct the development and design of the Interventional Phase (Phase 2) not yet enrolling.

02

Conditions studied

  • Oral Mucosa Discomfort
  • Pediatric Cancer
  • Mucositis Oral

Keywords

  • Music Therapy
03

In context

Neoplasms

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

This study's planned enrollment of 50 is below the median of 60 across 7,703 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,169 studies on the registry; 372 are open to participants now.

Of its 267 completed or terminated interventional studies of FDA-regulated products, 202 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Phase 1

  • Child ages 6-18 years old
  • Child has received music therapy and experienced oral mucositis
  • Parent/guardian 18 years and older
  • Able to communicate in English

Exclusion criteria

Exclusion Criteria:

Phase 1

  • Diagnosis of a developmental disorder that would prevent engagement in the active music-making or passive music-listening intervention or completion of study measures.
  • Significant pre-existing hearing loss or impairment that would interfere with participation in the interventions.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Other
    Phase 1: Interview

    Participants will consist of parent-child dyads and will take part in an interview conducted online (over Zoom) about the child's experiences with oral mucositis and perceptions of music therapy while experiencing oral mucositis pain. The interview is expected to last up to 1 hour.

    Other: Semi-Structured Interviews

Interventions

  • OtherSemi-Structured Interviews

    Participants will be interviewed online via Zoom

06

What researchers measure

Primary outcomes

  1. Identify patterns in previous experience with music therapy

    Semi-structured interviews will be audio/video-recorded and transcribed using Zoom's built-in transcription function. Finalized transcripts will be analyzed using reflexive thematic analysis, a qualitative method for identifying and interpreting patterns within the data.

    Time frame: 1 day

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — De-identified data collected may be shared with study collaborators during the course of the study.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Dec 2026; primary completion for Sep 2027, 9 months later.

Of 1,981 non-industry interventional studies with no phase under Neoplasms, half reached primary completion within 29 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 52. This study's planned 9 months is below that.

Counting every sponsor, half of 2,056 studies reached it within 29 months; a quarter within 13 and three quarters within 52.

Neoplasms covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 15, 2026: start Sep 2026 → Dec 2026, primary completion Jul 2027 → Sep 2027 and completion Jul 2027 → Sep 2027.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Jun 11, 2026
First posted
Jun 17, 2026
StartEst.
Dec 15, 2026was Sep 2026
Primary completionEst.
Sep 30, 2027was Jul 2027
CompletionEst.
Sep 30, 2027was Jul 2027
Last update
Oct 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Start date
Sep 1, 2026→Dec 15, 2026
Oct 15, 2026
Primary completion
Jul 31, 2027→Sep 30, 2027
Oct 15, 2026
Study completion
Jul 31, 2027→Sep 30, 2027
Oct 15, 2026
Show all 1 update
  1. Oct 15, 2026
    Start date Sep 1, 2026→Dec 15, 2026
    Primary completion Jul 31, 2027→Sep 30, 2027
    Study completion Jul 31, 2027→Sep 30, 2027
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07653360
Collaborators
Perloff Family Foundation
Responsible party
Sponsor
First posted
Jun 17, 2026
Start date
Dec 15, 2026 (estimated)
Primary completion
Sep 30, 2027 (estimated)
Completion
Sep 30, 2027 (estimated)
Last update
Oct 15, 2026

Study contacts

Jonathan Tang, MT-BC, PhD
Contact
Jonathan.Tang2@ucsf.edu
(415) 353-3327
Wei Li Jonathan Tang, MT-BC, PhD
principal investigator · University of California, San Francisco

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion