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Music Listening for Chronic Pain (FAMILIA Trial)
FAMILIA Trial Summary
This trial looks at whether two music interventions can help people with chronic pain and whether they are acceptable to patients.
FAMILIA Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.FAMILIA Trial Design
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Who is running the clinical trial?
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- You are not currently receiving music therapy services.You are currently receiving treatment through music therapy.You are currently having thoughts of harming yourself and have a plan to do so.You have hearing or thinking problems that may affect your ability to listen to music or imagine things.You have been experiencing moderate to severe musculoskeletal pain for at least six months. On a scale of 0 to 10, your pain level is at least 5.
- Group 1: Music Imagery
- Group 2: Music Listening
- Group 3: Usual care
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Is this clinical research available to participants at the present time?
"Affirmative. Clinicaltrials.gov data shows that, since its initial posting on September 1st 2021 and last modification on June 28th 2022, this study is actively seeking participants with an aim of recruiting 60 individuals from a single site."
How many participants have volunteered for this clinical trial?
"Affirmative. Clinicaltrials.gov documents the fact that this clinical trial, which became visible on September 1st 2021, is still open for recruitment. 60 individuals need to be welcomed from one centre in total."
What specific end goal is the research team striving to achieve?
"The primary aim of this 3-month clinical trial is to evaluate how many eligible veterans accept and complete the study's protocol, including intervention sessions. Secondary objectives include an assessment of pain interference using the Brief Pain Inventory (score range: 0 - 10; higher scores indicating more disruption), a Centrality of Pain Scale (score range: 10 - 50; worse outcomes associated with greater centrality) and a Numerical Rating Scale for Pain Intensity (score range: 0 - 10; higher values representing increased intensity)."
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