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Clinical Trials in Spain / NCT07106255
Enrolling by invitation Not applicable

Task-oriented Training Intervention for Multiple Sclerosis Patients.

NCT07106255 · tracked via the Priya Life Science Spain tracker
Sponsor
Universidad de Granada
Phase
Not applicable
Started
2024-09-01
Last updated
2025-08-06

Condition(s) studied

Multiple Sclerosis

Investigational drug(s) / intervention(s)

Task-oriented trainingStandar medical care and leaflet fatigue management

Task-oriented training: Participants included in the experimental group will underwent an 8-week TOT intervention, administered twice weekly, with each session lasting 45 minutes. Within this framework, the intervention will comprise sessions involving meaningful and repetitive activities tailored to both the patient and their specific context. The occupations will be selected by each participant through the Canadian Occupational Performance Measure (COMP) tool in the initial assessment. The activities were randomly ordered and focused on the reconstruction of complete tasks. To support task segmentation, a range of custom-designed materials will be employed, alongside therapeutic tools and materials such as therapeutic putty, TheraBand, and others commonly used in physical rehabilitation interventions. Throughout the intervention, participants will receive positive reinforcement that will fade over the time to prevent unnecessary dependency.

Standar medical care and leaflet fatigue management: Participants included in the control group will continue with their usual treatment and will receive a pamphlet containing information on fatigue management.

Study summary

This study aims to evaluate the effectiveness of a Task-oriented program in improving functional performance and health outcomes in patients with Multiple Sclerosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of Multiple Sclerosis by a neurologist. * Aged over 18 years old. * Acceptance and signature of the informed consent. Exclusion Criteria: * A cognitive level or condition that did not allow completion of the evaluations. * An exacerbation of MS during the previous 3 months. * Presence of interfering musculoskeletal, neurological, orthopaedic, and/or rheumatic disorders affecting hand and/or finger mobility, including previous trauma or fracture of the upper extremity.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Health Sciences. University of Granada Granada Granada

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Other trials for the same condition

Pregnancy Exposure Registry for Vumerity (Diroximel Fumarate) Recruiting
Short Sprint Interval Training in People With Multiple Sclerosis Recruiting
Safety and Efficacy of Fingolimod in Pediatric Patients With Multiple Sclerosis Active, not recruiting
Effects of DHA in Patients With Multiple Sclerosis Enrolling by invitation
Pilot Study of tSCS for Improving Upper Limb Function in People With Multiple Sclerosis Starting soon
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07106255 on ClinicalTrials.gov ↗ ← All trials in Spain