Impact of the Implementation of Dance Therapy Workshops on the Quality of Life of Adults With Disabilities Institutionalized Within the Medico-social Establishments of the Univi Group
NCT ID: NCT05915533
Last Updated: 2025-05-15
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
57 participants
INTERVENTIONAL
2023-09-08
2024-09-08
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The Associative Group UNIVI wants to evaluate through this study the effects of the practice of dance on the quality of life of the disabled adults accomodates in social medical establishments of UNIVI group
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of the Implementation of Dance Therapy Workshops on the Quality of Life of Dependent Elderly People Institutionalized Within the Establishments of the Univi Group
NCT05436574
Community Based Music and Dance Movement Therapy Group for Older Adults With Dementia
NCT03404050
Dance Intervention to Improve Executive Function and Physical Performance in Older Adults With Cognitive Impairment
NCT07105800
Movement and Music Intervention for Individuals With Dementia
NCT03121950
danceSing Care Evaluation: Testing the Feasibility
NCT05559203
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The dance therapy will be deployed in all the medico-social establishments participating in the study over a period of 12 weeks.
To do this, dance therapists will be recruited to provide these classes.
The dance-therapy will be carried out:
* in groups of 10 to 12 people who have given their informed consent,
* at least twice a week per group,
* over a period of 30 to 45 minutes maximum twice a week for 3 months. Several groups per establishment can be planned depending on the number of people who can and want to be included in the dance workshop.
940 participant in the study will be inclued and followed at 1 month, 3 months and 6 months after the end of the dance therapy workshops.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Before/after study
Dance therapy
Before/after study to measure the effects of the dance therapy activity on the quality of life of the disabled adults housed in the establishments of UNIVI group.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Dance therapy
Before/after study to measure the effects of the dance therapy activity on the quality of life of the disabled adults housed in the establishments of UNIVI group.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* informed consent to participate in the study
* Participant with a minimum of language skills to understand instructions and simple questions
Exclusion Criteria
* Adults with disabilities temporarily housed
* Severe cognitive and/or behavioral disorders that do not allow you to follow a dance workshop
* Permanent bed rest
* Non-affiliation to a social security scheme
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Médical Porte Verte
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hopital La Porte Verte
Versailles, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023-A01119-36
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.