Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
80 participants
INTERVENTIONAL
2024-03-01
2025-07-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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No Intervention: Control Group
Patients who receive the treatment program, will previously constitute their own control group (waiting list control group).
No interventions assigned to this group
Experimental group
Patients admitted to the brain injury unit will participate in a music therapy protocol starting one week after admission. Prior to the group session, three evaluations will be conducted over six days. Post-treatment assessments will also be conducted to enable longitudinal evaluation of the patient over the course of a week.
MERAKI_ABI
The music therapy session will focus on the themes of reidentification and involvement. The aim is to accompany the patient during the illness process, allowing them to express their emotional state, relate to music, promote listening and communication between family members, help and value preserved abilities, and promote personal involvement in the rehabilitation process.
The session will work with songs, taking into account musical preferences.
Interventions
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MERAKI_ABI
The music therapy session will focus on the themes of reidentification and involvement. The aim is to accompany the patient during the illness process, allowing them to express their emotional state, relate to music, promote listening and communication between family members, help and value preserved abilities, and promote personal involvement in the rehabilitation process.
The session will work with songs, taking into account musical preferences.
Eligibility Criteria
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Inclusion Criteria
* Be over 18 years of age.
* The participant or their relatives have signed the informed consent form.
* They have completed the group music therapy intervention session, as well as the pre-test and post-test evaluations.
Exclusion Criteria
* The Barthel Index score is below 60, indicating functional dependency.
18 Years
ALL
No
Sponsors
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University of Valencia
OTHER
Responsible Party
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M. Antonia Pérez-Marín
Associate Professor
Principal Investigators
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Marián Pérez-Marín, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Valencia
Locations
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Hospital Dr. Moliner
Serra, Valencia, Spain
Countries
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Central Contacts
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Facility Contacts
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Miguel Fombuena, PhD
Role: primary
Selene Valero-Moreno, PhD
Role: backup
Isabel Bellver Vercher
Role: backup
Ana Alegre Soler
Role: backup
José Jorge Botella Trellis, Dr.
Role: backup
Cristina Rocío Espejo Fernández, Dra.
Role: backup
María Carmen Badía Picazo, Dra.
Role: backup
Other Identifiers
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Meraki_Acquired Brain Injury
Identifier Type: -
Identifier Source: org_study_id