Mental Imagery on Upper Extremity Skills

December 18, 2025 updated by: Hatice Adiguzel, Kahramanmaras Sutcu Imam University

The Immediate Effect of Mental Imagery on Upper Extremity Skills With the Patients of Parkinson's Disease

Parkinson's disease (PD) is the second most common neurodegenerative disease, characterized pathologically by the progressive loss of dopaminergic neurons in the substantia nigra and clinically by the presence of motor symptoms such as bradykinesia, resting tremor, and/or rigidity. Among the motor deficits frequently observed in PD, patients are known to frequently report difficulties with manual dexterity. Many upper extremity and manual dexterity deficits are present in PD. Motor imagery (MI) is the imaginal execution of motor activities or the activation of specific muscles in the absence of any explicit feedback. This area of rehabilitation has been shown to be effective in improving and developing motor skills in many neurological conditions where patients exhibit motor recognition and execution impairments. MI can be applied at all stages of recovery from PD, is highly effective in movement-related pathologies, and can be performed independently.There is sufficient evidence that MI improves motor performance and learning in individuals with neurological disorders such as multiple sclerosis, stroke, and spinal cord injury. The study was designed to investigate the immediate effects of mental imagery, which is thought to be effective in controlling difficulties in planning and initiating movements in PD, on upper extremity skills. Therefore, the aim of this study was to determine the effect of mental imagery on upper extremity skills in PD.

Study Overview

Status

Recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: hatice Adiguzel tat, Associate Proffessor
  • Phone Number: +903443002647
  • Email: fzthatis@gmail.com

Study Contact Backup

  • Name: Hatice adıgüzel tat, Associate Proffessor
  • Phone Number: +903443002647
  • Email: fzthatis@gmail.com

Study Locations

    • Onikişubat
      • Kahramanmaraş, Onikişubat, Turkey (Türkiye), 46100
        • Recruiting
        • Kahramanmaraş Sütçü İmam University
        • Sub-Investigator:
          • Yusuf Şinasi Kırmacı, Asisstant Prof
        • Sub-Investigator:
          • Abdulkadir Ertürk, Msc
        • Sub-Investigator:
          • Tuğçe Simay Özbay, Msc
        • Sub-Investigator:
          • Buket Tuğan Yıldız, Associate Professor
        • Sub-Investigator:
          • Hatice adıgüzel tat, Associate Professor
        • Sub-Investigator:
          • Deniz Tuncel Berktaş, Proffessor
        • Principal Investigator:
          • Asiya uzun, Asisstant Prof
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Healthy individuals aged 40-75 years, diagnosed with idiopathic PD according to the UK Parkinson's Disease Association Brain Bank criteria by a specialist neurologist, with a Modified Hoehn & Yahr (m-HY) scale stage ≤4, and with a Mini Mental State Examination score of ≥24 for those with training and ≥18 for those without training, and with no known disease, volunteered to participate in the study.
  • PD individuals with no other known neurological and/or systemic disease
  • PD individuals without any upper extremity contractures

Exclusion Criteria:

  • Individuals with diagnosed and/or treated psychiatric illnesses who are considered unable to complete the tests.
  • Individuals who is taking neuroleptic medications or antidepressants.
  • Individuals with orthopedic conditions that interfere with manual dexterity tests, such as severe dyskinesia, carpal tunnel syndrome, tendon injuries, or finger amputations; rheumatological conditions such as rheumatoid arthritis and osteoarthritis; and individuals with any neurological condition other than PD.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 1/study group
Upper extremity skill tests will be performed on individuals diagnosed with idiopathic Parkinson's disease and recorded with a mental stopwatch using mental imagery.
The Nine-Hole Peg Test (9 DPT) will be performed with a mental chronometer.the duration between actually physically performing the movement and mentally imagining the same movement will be recorded.
No Intervention: 2/control group
Upper extremity skill tests will be performed on individuals diagnosed with idiopathic Parkinson's disease.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Nine-Hole Peg Test (9PPT) with Mental Chronometry
Time Frame: first day of the assesment

Mental Chronometry: Mental chronometry is a method that measures imagery time, considered more objective than questionnaires in the assessment of MI. It examines the time difference between the actual physical execution of a movement and the mental image of the same movement.

The Nine-Hole Peg Test (9PPT) is frequently used in the literature, although its validity and reliability as a mental chronometry test are lacking. In this task, the participant is required to remove nine pegs from the board to which they are fixed as quickly as possible and place them in a container on the board. The pegs used in the test (8 mm in diameter, 3 cm long) can be made of wood or plastic. The board (23 cm long, 10 cm wide, and 2 cm high) has a section at one end where the pegs are fixed (arranged in a 3x3 matrix) and a container-shaped space on the side for the pegs to be placed. Participants perform the test on both upper extremities. Before the test, all participants are given the opportunity to ho

first day of the assesment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
sosyodemographic form
Time Frame: first day of the assesment
Medical history (disease duration and symptoms), demographic information, will be recorded.
first day of the assesment
Modified Hoehn & Yahr (m-HY) scale
Time Frame: first day of the assesment
PD disability will be assessed with the m-HY scale. All of the patients with PD will be staged according to the Hoehn Yahr scale as follows: stage 1.0 (unilateral involvement only); stage 1.5 (unilateral and axial involvement); stage 2.0 (bilateral involvement without balance impairment); stage 2.5 (mild bilateral disease with improvement in the pull test); stage 3.0 (mild to moderate bilateral disease; some postural impairment; physically independent); stage 4.0 (severe disability; still able to walk or stand unaided).
first day of the assesment
Unified Parkinson's Disease Rating Scale (UPDRS)
Time Frame: first day of the asessment
Symptom severity in PD is rated using the Unified Parkinson's Disease Rating Scale (UPDRS). Several items on this scale assess upper extremity and hand function. The Activities of Daily Living section assesses handwriting, cutting food, and grasping utensils. The Motor section assesses finger tapping, hand movements, and rapid alternating hand movements. These test items are scored from 0 to 4, with 4 representing maximum impairment and 0 representing normal movement ability. The UPDRS sections are subdivided into: Section I (mental dysfunction and mood); Section II (activities of daily living); Section III (motor); and Section IV (treatment-related complications).
first day of the asessment
Mini Mental State Examination (MMSE)
Time Frame: first day of the assessment
This test was developed by Folstein in 1975. Its Turkish validity and reliability study was conducted by Güngen et al. in 2002. The MMSE, which is quite suitable for screening cognitive function in the elderly and assesses cognitive functions in five separate areas (orientation, registration, attention and calculation, recall, and language), is frequently used. A score below 24 on the MMSE indicates dementia, 24-26 indicates mild cognitive impairment, and 26 or above indicates normal cognitive function.
first day of the assessment
Muscle Strength Measurement
Time Frame: first day of the assesment
Isometric strength will be measured using a digital muscle strength measurement device (KFORCE KINVENT) for the bilateral serratus anterior, upper trapezius, latissimus dorsi, deltoid, supraspinatus, teres minor, subscapularis, and biceps brachii muscles of the upper extremity.
first day of the assesment
Grip Strength Measurement
Time Frame: first day of the assesment
A Jamar hand dynamometer (Baseline®) (and a PinchMeter (Baseline Mechanical Pinch Gauge with Case, Blue, 30 lb) will be used for grip strength measurement.
first day of the assesment
The Kinesthetic and Visual Imagery Questionnaire (KVIQ)
Time Frame: first day of the assesment
The Kinesthetic and Visual Imagery Questionnaire (KVIQ), Short Form, was developed to determine the extent to which individuals visualize and feel imaged movements. It consists of a total of 10 movements measuring five visual and five kinesthetic imagery skills (23). The questionnaire is not a self-report measure but is administered by an assessor. All movements are assessed in a sitting position. The assessor first performs the relevant movement on themselves, and then the participant is asked to perform the same movement only once. The participant then imagines the movement and is asked to rate the visual clarity or intensity of sensations of the imagined movement using a five-point ordinal scale. Higher scores indicate greater visual clarity or intensity of sensations. This questionnaire will be used to assess mental imagery ability in our study.
first day of the assesment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Yusuf Şinasi Kırmacı, Asisstant Prof, Kahramanmaraş Sütçü İmam University
  • Study Chair: hatice adıgüzel tat, Associate Professor, Kahramanmaraş Sütçü İmam University
  • Study Chair: Abdulkadir Ertürk, Msc, Kahramanmaraş Sütçü İmam University
  • Study Chair: Tuğçe Simay Özbay, Msc, Kahramanmaraş Sütçü İmam University
  • Study Chair: Buket Tuğan Yıldız, Associate Professor, Kahramanmaraş Sütçü İmam University
  • Principal Investigator: Asiya Uzun, Asisstant Prof, Kahramanmaraş Sütçü İmam University
  • Study Chair: Deniz Tuncel, Proffessor, Kahramanmaraş Sütçü İmam University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2025

Primary Completion (Estimated)

December 31, 2025

Study Completion (Estimated)

January 30, 2026

Study Registration Dates

First Submitted

September 12, 2025

First Submitted That Met QC Criteria

September 18, 2025

First Posted (Estimated)

September 25, 2025

Study Record Updates

Last Update Posted (Actual)

December 19, 2025

Last Update Submitted That Met QC Criteria

December 18, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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