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Recruiting NCT07218055

Assessment of Music Experiences in Navigating Depression Part 2

No phase Interventional Depression

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: Music therapy.
Who it may be relevant to
Registry conditions: Depression. Basic parameters: 7 years — 15 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
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Assessment of Music Experiences in Navigating Depression (AMEND)

Overview

This study is again looking at the use of music and music therapy experiences in navigating depression. The researchers will provide 11 sessions of music therapy and half will be followed by recitals at the Third Street School Music Settlement where the kids enrolled in our study will observe and interact with the performers and discuss and reflect on anxiety and performance and how sharing personal creativity affects them intra and interpersonally.

Detailed description

The researchers will provide hourly weekly music therapy sessions and then go to the Third Street Music School and work with their kids and our kids providing insights and feedback. The researchers will test their depression (CDI) and Resilience (Connor Davidson)

Interventions

  • Other Music therapy
    hourly weekly music therapy sessions

Primary outcome measures

  • Conor-Davidson Resilience Scale [Time frame: end of 6 months]
Secondary outcome measures (1)
  • CDI2 or Children's Depression Inventory, Second Edition [Time frame: end of 6 months]

Eligibility criteria

Inclusion criteria

  • Must indicate depression -or symptoms thereof by parent in writing
  • We are including children only in Amend II

Exclusion criteria

\- none

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

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Diagnostic

Study locations

United States · 1 center
  • Mount Sinai Union Square — New York

Identifiers

NCT: NCT07218055 · STUDY-22-01609-CR004 · STUDY-22-01609-CR004

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗