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Effects of Using Advanced NEUROrehabilitation TECHnologies in Upper Limb Motor Function and Capacity Recovery in People With Stroke

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

This study aims to evaluate the effect of a personalized technology-based rehabilitative intervention on Upper Limb (UL) motor function and capacity recovery in People with Stroke (PwS). The study is single-cohort study in which eligible participants will undergo baseline and follow-up clinical and instrumental assessments over a 4-5 week period. The intervention consists of a personalized and specific upper limb technology-based rehabilitation programme delivered three times per week for a total of 12-15 sessions. Each session lasts approximately one hour and is integrated with conventional rehabilitation treatments. Primary outcomes include Fugl-Meyer Assessment for Upper Extremity (FMA-UE) and Action Research Arm Test (ARAT). Secondary outcomes include instrumental assessment of active range of motion and grip strength.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years;

• First-ever unilateral ischemic or hemorrhagic stroke;

• Presence of upper limb motor impairment;

• Modified Ashworth Scale (MAS) \< 3;

• Montreal Cognitive Assessment (MoCA) \> 24;

• Medically stable and able to participate in an intensive rehabilitation programme;

• Ability to understand and follow study procedures;

• Written informed consent.

Locations
Other Locations
Italy
Fiorenzuola d'Arda Hospital - AUSL Piacenza
RECRUITING
Fiorenzuola D'arda
Contact Information
Primary
Gianfranco Lamberti, MD
g.lamberti2@ausl.pc.it
+39 0523 404656
Time Frame
Start Date: 2026-06-15
Estimated Completion Date: 2027-08
Participants
Target number of participants: 25
Treatments
PwS
Adult People with Stroke (PwS) with Upper Limb (UL) motor function impairment
Related Therapeutic Areas
Sponsors
Leads: Azienda Unita Sanitaria Locale di Piacenza

This content was sourced from clinicaltrials.gov