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Recruiting Not applicable

Influence of Autonomy on Motor Learning in People With Parkinson's Disease

NCT05960331 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2023-08-21
Last updated
2025-11-18

Condition(s) studied

Parkinson Disease

Investigational drug(s) / intervention(s)

Autonomy supported learningPractice with predetermined feedback

Autonomy supported learning: The ability of learners to participate in determining their own behaviour, which is the feedback schedule regarding their practice performance in this study.

Practice with predetermined feedback: Learners practice the motor task, while the feedback is provided according to their counterpartner

Study summary

The goal of this clinical trial is to explore the benefits of autonomy supported learning in patients with Parkinson's disease. The main questions to answer are:

* Whether autonomy supported learning can benefit motor learning in PD patients
* Whether autonomy supported learning can enhance intrinsic motivation and/ or information processing of PD patients in learning a new task.
* Whether autonomy supported learning can facilitate cortical excitability change after practicing a new task.

Participants will be recruited into two groups (Self-control group, SC; and yoked group, YK) to learn a finger-pressing trajectory matching task

* Participants in SC group will have choice over feedback schedule during trial practice
* Participants in YK group will receive feedback with no-choice during trial practice Researchers will compare the retention test performance to see if autonomy supported learning will lead to better learning effect.

Eligibility

Sex
ALL
Min age
20 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * age above 20-years-old * able to follow instructions to perform the tasks (Montreal Cognitive Assessment ≥ 24) * no surgery and injury in upper extremities in recent 6 months Exclusion Criteria: * other neurological disorders in addition to Parkinson's disease * Parkinson's disease dementia * symptom of severe tremor in upper extremities (score ≥ 3 in Question 15 to 18 of UPDRS-III) * deep brain stimulation or pacemaker implanted * medical history of seizure * a blood-relative with history of epilepsy * unstable medical conditions * pregnancy

Primary outcome measure(s)

  • Performance accuracy — up to day 7
    Overall performance accuracy relative to the target waveform was assessed using root mean square error (RMSE), which is the mean difference between the target waveform and the participant's movement trajectory calculated over their actual movement time.

Trial sites (1)

FacilityCityRegionStatus
National Taiwan University Hospital Taipei Taiwan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05960331 on ClinicalTrials.gov ↗ ← All trials in Taiwan