- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06219265
Neuropsychological and Electrophysiological Effects of Dance Therapy With People With Severe Mental Disorders
A single-centre prospective randomised controlled trial will be conducted with a minimum of 47 patients with severe mental disorder (SMD) who will be randomly assigned into two groups, 1 intervention group receiving dance therapy (n=26) and 1 control group who will not receive any intervention or added treatment apart from continuing with their usual treatment (pharmacological), but will not receive intervention with dance therapy (n=21).
In summary, the groups are:
- Experimental group (n=26): people with SMD receiving dance therapy.
- Control group (n=21): people with SMD who do not receive the dance therapy intervention but do receive their usual pharmacological treatment.
Tests will be administered before the start of the study and at the end of the study, as well as 3 months after the end of the study in order to compare the results between groups.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
All the tests (BASC, MoCA, PANSS and EEG) will be carried out with the 47 patients with SMD to find out their baseline status. The people with SMD will be randomly assigned to an experimental group (dance therapy program) or a control group (without intervention in dance therapy but with regular pharmacological treatment). The study will last approximately 1 year between the administration of tests, the program and the analysis of results. The dance therapy program will last 20 sessions over 10 weeks. The sessions will take place at the headquarters of the Canarian Association of Creative Therapies (ASCATEC) in the 21st century space in Santa Cruz de Tenerife.
The 26 people with SMD in the experimental group will participate in a 10-week intervention program with 2 sessions per week in which they will work for 1 hour on memory, attention and executive functions through dance and movement, ending with 10 minutes of Mindfulness.
The 21 people in the control group will not receive any type of dance therapy intervention, but will continue with their usual pharmacological treatment.
The effects will be measured after a treatment of 20 sessions (twice a week). Results will be obtained by analysing EEG parameters (EEG amplitude and frequency) and cognitive functions (BACS and MoCA). On the other hand, at the end of the 20-session programme, tests will also be administered to assess the symptomatology of the severe mental disorder suffered by the person (PANSS) to assess the effects of the program on these variables.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Islas Canarias
-
Santa Cruz De Tenerife, Islas Canarias, Spain, 38003
- ASCATEC
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Persons diagnosed with a serious mental disorder according to the Diagnostic and Statistical Manual of Mental Disorders -V.
- Have the capacity to decide and consent.
- Be between 18 and 75 years of age.
- No active consumption of toxic substances (except nicotine).
- Commitment to attend for the entire study period from December 2023 to December 2024.
Exclusion Criteria:
- Not having given free consent to participate in the study.
- Having a comorbid severe mental disorder, associated intellectual disability, history of severe brain damage or neurological disorder that may function as a confounding factor (Associated organic-type disorder, borderline or lower IQ)
- Active substance abuse (except nicotine)
- Having a cochlear implant, fixed hearing aids or plates in the head.
- Having suffered a concussion to the head with loss of consciousness that subsequently triggered symptoms related to the pathology.
- Having suffered from epileptic seizures.
- Not having the desire to participate in dance therapy sessions for any reason or to undergo electroencephalogram testing.
- Currently involved and participating in another cognitive rehabilitation program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group 1: people with SMD receiving dance therapy
Intervention group of people with SMD (n=26) who receive a 20-session dance therapy program for 10 weeks with 2 sessions per week in which they work for 1 hour on memory, attention and executive functions through dance and movement, ending with 10 minutes of Mindfulness.
|
A single-centre prospective randomised controlled trial will be conducted with a minimum of 48 patients with severe mental disorder (SMD) who will be randomised into two groups, 1 intervention group receiving dance therapy (n=24) and 1 control group receiving no intervention or treatment (n=24). In addition, there will be an intervention group of healthy people who will receive dance therapy (n=20). All the tests, will be carried out with patients with SMD and only the EEG for healthy people, in order to determine their baseline state. The dance therapy program will last for 20 sessions over 10 weeks. The 44 people in the two experimental groups will participate in a 10-week intervention program with 2 sessions per week in which they will work for 1 hour on memory, attention and executive functions through dance and movement, ending with 10 minutes of Mindfulness. The 24 people in the control group will not receive any type of intervention. |
|
No Intervention: Control group: people with SMD who do not receive any intervention
This group of 21 persons with SMD will not receive any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brief Assessment of Cognition in Schizophrenia (BACS)
Time Frame: At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
It is used to quantify cognitive impairment in schizophrenia. BACS includes assessments of verbal memory, working memory (Digit Span), motor speed (Motor Token), verbal fluency, attention and processing speed (Symbol Encoding) and executive function (Tower of London). Each item assessed has its own specific score. These scores are used to assess performance on each of the BACS subtests. Subsequently, a composite score is usually calculated that summarises the individual's overall cognitive performance. |
At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
|
Montreal Cognitive Assessment (MoCA)
Time Frame: At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
30-question test to assess mild cognitive dysfunction by assessing executive function and visuospatial ability, identification, short-term memory, delayed recall, attention, language, abstraction, animal naming and orientation.
Scores range from 0 to 30 and the cut-off point value for a normal score is >26 points.
The test is administered in about 10-12 minutes.
|
At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
|
Electroencephalogram (EEG)
Time Frame: At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
The brain wave signals shall be recorded by a 14-channel electroencephalogram, whose electrodes (salt sensors) are arranged at positions A F 3, F7, F3, F C 5, T7, P7, O1, O2, P8, T8, F C 6, F4, F8 and A F 4, according to the international 10-20 system.
The device also has 2 reference points at positions P3 and P4.
|
At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Positive and Negative Symptom Scale (PANSS)
Time Frame: At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
It monitors the progress of symptoms in severe mental disorders by means of 30 items that are grouped into three main dimensions: positive symptoms, negative symptoms and general symptoms.
Each item is scored from 0 (no symptoms) to 7 (extreme severity) points.
|
At baseline, up to 10 weeks of dance therapy program and 3 months after the end of the program.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Nayra Caballero Estebaranz, ASCATEC and European University of the Canary Islands
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
- TFM_01_DANZA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Severe Mental Disorder
-
Alejando Vargas RubioCompletedSevere Mental Disorder | Severe Mental IllnessSpain
-
Alejando Vargas RubioActive, not recruitingSevere Mental Disorder | Severe Mental IllnessSpain
-
IRCCS Centro San Giovanni di Dio FatebenefratelliRecruitingSevere Mental Disorder | Severe Mental IllnessItaly
-
Instituto Nacional de Psiquiatría Dr. Ramón de...Columbia University; Research Foundation for Mental Hygiene, Inc.; Instituto...Enrolling by invitation
-
Norwegian Institute of Public HealthUniversity of Tromso; Nordlandssykehuset HF; University of Melbourne; The University... and other collaboratorsUnknownSevere Mental DisorderNorway
-
Versailles HospitalAgence régionale de santé Ile de France; UNION NATIONALE DE FAMILLES ET AMIS...Not yet recruiting
-
University of Roma La SapienzaNot yet recruitingSevere Mental Disorder
-
Temple UniversityNational Institute on Disability, Independent Living, and Rehabilitation...CompletedSevere Mental DisorderUnited States
-
University of BernUniversity of Zurich; Swiss National Science FoundationCompletedSevere Mental DisorderSwitzerland
-
Fundació Institut de Recerca de l'Hospital de la...University Ramon LlullActive, not recruiting
Clinical Trials on Dance Therapy
-
Ospedale Generale Di Zona Moriggia-PelasciniUnknown
-
University of Illinois at ChicagoNational Institute on Aging (NIA)CompletedMild Cognitive Impairment | Older Adults | Neurological InjuryUnited States
-
Centre Médical Porte VerteNot yet recruiting
-
Centre Hospitalier Emile RouxRecruiting
-
Centre Médical Porte VerteCompleted
-
Helsinki University Central HospitalUniversity of Helsinki; Finnish Institute for Health and Welfare; Finnish Medical...Recruiting
-
Ankara Medipol UniversityCompletedMotor Skills | Dyslexia | Executive Function | Dance TherapyTurkey
-
Hospices Civils de LyonNot yet recruitingChronic Pain | Complex Regional Pain Syndromes | Tension-Type HeadacheFrance
-
The University of Hong KongTung Wah Group of HospitalsCompleted