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Clinical Trials/NCT02150395
NCT02150395CompletedNot Applicable

The Impact of Music Therapy on Anxiety in Patients Newly Diagnosed With Cancer & Undergoing Simulation for Radiation Therapy

Beth Israel Medical Center1 site in 1 country82 target enrollmentStarted: July 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
82
Locations
1
Primary Endpoint
Reduction in state anxiety

Study Overview

Brief Summary

This study looks at the effects of a protocolized music therapy intervention on state anxiety for patients with cancer undergoing simulation for radiation therapy. Simulation, which is an imaging and diagnostic procedure, has been identified as producing significantly high levels of anxiety in many cancer patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Newly diagnosed patients with breast cancer, and newly diagnosed patients with head and neck cancer.
  • •18 or over.
  • •Fluent in English.

Exclusion Criteria

  • •Under 18 years.
  • •Pre-existing anxiety disorders.

Arms & Interventions

music therapy

Experimental

pt received a protocolized music therapy intervention that included altered state induction, music driven guided visualiztion, and psychoeducation on relaxation techniques to be used during simulation for radiation therapy. Prescribed pre-recorded music program provided to be used during simulation.

Intervention: music therapy (Other)

control

No Intervention

no intervention

Outcomes

Primary Outcomes

Reduction in state anxiety

Time Frame: 20 minutes

pt received a protocolized music therapy intervention that included altered state induction, music driven guided visualiztion, and psychoeducation on relaxation techniques to be used during simulation for radiation therapy. Prescribed pre-recorded music program provided to be used during simulation.

Secondary Outcomes

  • reduced distress(20 minutes)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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