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Enrolling by invitation NCT06576219

'My Life is Music' Group Therapy Model - a Feasibility Study for Adolescents With Persistent Pain

No phase Interventional Pediatric Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Group Music Therapy.
Who it may be relevant to
Registry conditions: Pediatric Pain. Basic parameters: 13 years — 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Finland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of this multi-method feasibility study is to learn if a group therapy model using music can be applied in the treatment of adolescents with persistent pain. We are interested how the patients find participating in the group therapy as part of their rehabilitation and if the patient´s experience of music changes during the therapy process.

Interventions

  • Behavioral Group Music Therapy
    My Life Is Music group therapy model

Primary outcome measures

  • Semi-structured interviews [Time frame: 12 weeks]
  • Patient Diaries [Time frame: Weekly entries for 8 weeks during intervention]
Secondary outcome measures (3)
  • PROMIS Pediatric Profile [Time frame: Baseline, 12 weeks]
  • Music Questionnares [Time frame: Baseline, 12 weeks]
  • Feedback Informed Treatment (FIT) [Time frame: Baseline, weekly entries for 8 weeks during intervention]

Eligibility criteria

Inclusion criteria

  • persistent pain (3 months)
  • fluency in finnish language

Exclusion criteria

\- a psychiatric illness that significantly impairs functioning

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Finland · 1 center
  • New Children´s Hospital — Helsinki

Identifiers

NCT: NCT06576219 · HUS/564/2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗