Robotic Neurorehabilitation in Patients With Ataxia | NCT07733687

NCT07733687

Overview

NCT ID: NCT07733687
Lead Sponsor: Somogy Megyei Kaposi Mór Teaching HospitalOTHER
Official Title: Assessment of the Effectiveness of Robotic Neurorehabilitation Treatment in Patients With Ataxia
Brief Summary: This interventional study evaluates the effectiveness of robot-assisted neurorehabilitation in patients with ataxia. Participants will receive a structured robotic neurorehabilitation treatment program, and changes in motor function, coordination, balance, gait, and functional performance will be assessed using clinical outcome measures before and after the intervention.
Conditions: Ataxia - Other
Interventions: Robot-Assisted Neurorehabilitation

Status and Timeline

Status: Active, not recruiting
Last Update Posted: Jul 29, 2026Actual
Start Date: Jun 2, 2026Actual
Primary Completion Date: Nov 2, 2027Estimated
Completion Date

Participation Criteria

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: All
Accepts Healthy Volunteers?: Yes
Eligibility Criteria: Inclusion Criteria:

Adults diagnosed with ataxia

Age 18 years or older

Ability to participate in a robot-assisted neurorehabilitation program

Stable clinical condition allowing participation in rehabilitation treatment

Ability to understand and follow study instructions

Ability to complete the planned clinical and functional assessments

Written informed consent provided by the participant

Exclusion Criteria:

Severe cognitive impairment preventing cooperation with the intervention or assessments

Severe musculoskeletal or neurological condition that prevents safe participation in robot-assisted rehabilitation

Unstable cardiovascular, respiratory, or other medical condition contraindicating rehabilitation treatment

Severe pain or orthopedic limitation preventing participation in the rehabilitation program

Severe visual or vestibular impairment that would interfere with study assessments

Acute medical condition or acute neurological deterioration at the time of enrollment

Participation in another interventional clinical study that could affect the study outcomes

Pregnancy, if participation is considered unsafe by the investigator

Any condition judged by the investigator to make participation unsafe or unsuitable

Study Plan

Study Type: Interventional
Phase: Not Applicable
Enrollment: 100Estimated
Primary Purpose: Treatment
Allocation: Randomized
Interventional Model: Single Group Assignment
Masking: None (Open Label)

Contacts and Locations

Central Contacts: No data available
Locations: Somogy County Kaposi Mór Teaching Hospital

Similar Studies

Participant Group/Arms

Robot-Assisted NeurorehabilitationExperimental

Participants in this arm will receive robot-assisted neurorehabilitation treatment aimed at improving motor function, coordination, balance, gait, and functional mobility in patients with ataxia.

Other: Robot-Assisted Neurorehabilitation

Conventional NeurorehabilitationActive Comparator

Participants in this arm will receive conventional neurorehabilitation according to standard clinical practice. Outcomes will be assessed using the same clinical and functional measures as in the robot-assisted neurorehabilitation arm.

Other: Conventional Neurorehabilitation

Control GroupNo Intervention

Participants in this arm will not receive robot-assisted neurorehabilitation as part of the study. They will undergo the planned clinical and functional assessments for comparison with the intervention arm.