Parkinson's Disease Clinical Trials

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Effects of Dual-Task Training on Upper Extremity Function and Muscle Thickness in Parkinson's Disease

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to investigate the effects of dual-task training on upper extremity function and muscle thickness in individuals with Parkinson's disease. The main questions it aims to answer are: Does dual-task training improve upper extremity function in individuals with Parkinson's disease? Does dual-task training lead to changes in upper extremity muscle thickness measured by ultrasonography? Researchers will compare a dual-task training group with a control group receiving routine care to determine whether 8 weeks of dual-task training results in greater improvements in upper extremity outco Participants will: complete baseline and post-intervention assessments of upper extremity function, muscle thickness, grip strength, and pinch strength be assigned to either a control group or a dual-task training group receive dual-task training 3 days per week for 8 weeks if assigned to the intervention group

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 65
Healthy Volunteers: f
View:

• Diagnosis of idiopathic Parkinson's disease confirmed by a neurologist

• Modified Hoehn and Yahr stage 2 to 3

• No medication or dosage change within the last 6 months

• Cognitive capacity sufficient to understand and follow instructions, defined as Montreal Cognitive Assessment score ≥21

• Voluntary participation with written informed consent

Locations
Other Locations
Turkey
Hacettepe University
RECRUITING
Ankara
Contact Information
Primary
Büşra Seçkinoğulları Korkusuz, PhD
bskorkusuz@ankara.edu.tr
+905442436914
Time Frame
Start Date: 2026-04-24
Estimated Completion Date: 2026-08-01
Participants
Target number of participants: 38
Treatments
Experimental: Dual-Task Training Group
Participants will receive dual-task training in addition to their routine daily activities. The training program will be performed 3 times per week for 8 weeks, with each session lasting 60 minutes and consisting of combined motor and cognitive tasks.
No_intervention: Control Group
Participants will continue their routine daily activities without receiving any additional exercise, training, or rehabilitation intervention during the study period.
Related Therapeutic Areas
Sponsors
Leads: Ankara University
Collaborators: Hacettepe University

This content was sourced from clinicaltrials.gov