NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

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

RecruitingNA

Sponsor: Ankara University

Conditions: Parkinson Disease (PD)

Interventions: Dual-Task Training

Countries: Turkey (Türkiye)

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 overview

Sex: ALL

Age: 40 Years to 65 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* 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

Exclusion Criteria:

* Atypical or secondary parkinsonism
* Advanced orthopedic condition affecting the upper extremity
* Surgery, trauma, or immobilization involving the upper extremity within the last 6 months
* Wound or dermatological condition preventing upper extremity ultrasonographic evaluation
* Severe visual or hearing loss
* Severe depression, psychosis, or communication difficulty
* Any additional health problem preventing regular participation in the study

Locations (1)

Ankara, Turkey (Türkiye)