- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06600685
Functionally Oriented Music Therapy (FMT) In The Treatment Of Long Term Pain
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Eskilstuna
-
Eskilstuna, Eskilstuna, Sweden, 633 42
- FMT centrum
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- People with long-term musculoskeletal pain that occurred for at least three months.
- People over 18 years of age.
- People able to understand and speak Swedish or English
Exclusion Criteria:
- Severe hearing loss
- Visual impairment
- Cognitive impairment.
Pain conditions caused by:
- malignancy
- severe spinal pathology or
- neurological disease that severely limit the ability to perform activities.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: FMT arm
|
There are different methods of music therapy and one of these is FMT.
It is a body-based and music therapeutic treatment method that is used for health-promoting purposes.
With the help of i.e. drums, cymbals, various custom-made drumsticks, flutes, chairs, balance balls and balance cushions.
FMT strives to support, strengthen and develop the person's physical, mental and social abilities.
FMT-sessions (20 minuets/1 time a week) are performed individuelly (a patient with a educated music therapist).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improved quality of life
Time Frame: Assessed every 2 weeks for 10 weeks.
|
Support, strengthen and develop the person's physical, mental and social abilities. Questionnaires concerning; body awareness, pain level, management of pain and fear of movement, pain-related activity limitations, emotions, depressive symptoms and anxiety, self-reported sick-leave and general perceived health will be used. The questionnaires are validated and psychometrically evaluated. Self-estimation (using different Lickert-scales). The results of phase 1 can contribute to the addition of more outcome measures in phase 2. |
Assessed every 2 weeks for 10 weeks.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-04082-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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