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Study identifier: NCT06906679 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Upper Limb Rehabilitation in People With Parkinson's Disease:

Condition: Parkinson Disease  ·  Sponsor: IRCCS San Raffaele Roma

PhaseNA
Planned participants40
Who can joinAll sexes, 30 Years to 80 Years
Healthy volunteersNo

About this study

This study evaluates the effectiveness of upper limb rehabilitation using an end-effector robotic device with exercises designed to improve movements, strength, and coordination of the shoulder, elbow, and wrist in patients with Parkinson's disease who have mild to moderate disability, compared to conventional rehabilitation treatment. The study protocol will involve individuals diagnosed with PD according to the UK Parkinson's Disease Society Brain Bank criteria, who will be randomly assigned to one of the following groups: A - Experimental Group (EG) - robotic treatment for upper limb rehabilitation. B - Control Group (CG) - conventional treatment for upper limb rehabilitation. Secondary objectives include: \- Evaluating the effectiveness of an end-effector robotic system in terms of improving upper limb coordination and functionality through the ARAT test and the UPDRS. Identifying subgroups of participants who may benefit more from robotic therapy based on PD disease stage (Hoehn \& Yahr), age, and upper limb impairment. Analyzing the effects of robotic rehabilitation on quality of life. Assessing participants' compliance and satisfaction levels with the robotic system in terms of improving participation in upper limb rehabilitation.

This description comes directly from the study's public registry record.

Talk to the study team

Dr. Sanaz Pournajaf, DPT  ·  +39 0652252405  ·  sanaz.pournajfa@sanraffaele.it

Dr. Carrie Louise Thouant, OT  ·  carrielouise.thouant@sanraffaele.it

Always discuss trial participation with your own doctor first.

Locations (2)

San Raffaele CassinoCassino, FR, ItalyNot Yet Recruiting
IRCCS San Raffaele RomaRome, Lazio, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06906679