- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07193303
- Original Trial
Mental Imagery on Upper Extremity Skills
The Immediate Effect of Mental Imagery on Upper Extremity Skills With the Patients of Parkinson's Disease
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
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
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Kahramanmaraş, Onikişubat, Turkey (Türkiye), 46100
- Recruiting
- Kahramanmaraş Sütçü İmam University
-
Sub-Investigator:
- Yusuf Şinasi Kırmacı, Asisstant Prof
-
Sub-Investigator:
- Abdulkadir Ertürk, Msc
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Sub-Investigator:
- Tuğçe Simay Özbay, Msc
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Sub-Investigator:
- Buket Tuğan Yıldız, Associate Professor
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Sub-Investigator:
- Hatice adıgüzel tat, Associate Professor
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Sub-Investigator:
- Deniz Tuncel Berktaş, Proffessor
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Principal Investigator:
- Asiya uzun, Asisstant Prof
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Contact:
- Asiya Uzun, assistant professor
- Phone Number: +903443002621
- Email: asiyeaycicek@gmail.com
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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.
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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
|
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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
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
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- mental imagination
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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