Actively Recruiting
Effects of Group Leisure Activities and Musical Training on Hospital Stroke Rehabilitation.
Led by Escola Universitària d'Infermeria i Teràpia Ocupacional de Terrassa · Updated on 2026-04-21
90
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
Sponsors
E
Escola Universitària d'Infermeria i Teràpia Ocupacional de Terrassa
Lead Sponsor
U
University Rovira i Virgili
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn whether adding group leisure activities and musical training can help people recover better after a stroke during their hospital rehabilitation. The study will include adults who had a recent stroke and are staying in the neurological rehabilitation unit. The main questions the study aims to answer are: Does adding leisure activities and musical training help people become more independent in their daily activities? Does this combined approach improve movement, thinking skills, mood, and quality of life more than standard rehabilitation alone? Researchers will compare three groups to see which approach works best: Standard hospital rehabilitation. Standard rehabilitation plus individual musical training. Standard rehabilitation plus group leisure activities and group musical training. Participants will: Take part in their usual rehabilitation sessions in the hospital. Depending on their assigned group, also do individual or group musical training and/or group leisure activities. Complete evaluations at the start of the study, at hospital discharge, and one month later. Have a brain scan and wear a wrist device that tracks daily movement. Share their experiences in an interview.
CONDITIONS
Official Title
Effects of Group Leisure Activities and Musical Training on Hospital Stroke Rehabilitation.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Diagnosis of ischemic or hemorrhagic stroke confirmed by neuroimaging
- Stroke occurred less than 4 weeks before enrollment
- Doctor's evaluation occurred less than 48 hours before enrollment
- No previous stroke with lasting motor or cognitive deficits
- Ability to provide informed consent and follow study procedures
- Neurological or major psychiatric conditions must be clinically stable if present
- Ability to understand Spanish, Catalan, or English
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
Physical Medicine and Rehabilitation Department, Esperança Centre, Hospital del Mar; Parc de Salut Mar (PSMar)
Barcelona, Catalonia, Spain, 08024
Actively Recruiting
Research Team
J
Jennifer Grau Sánchez, PhD
CONTACT
D
Dra. Cindry Ramírez Fuentes, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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