- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03589872
The Fine Motor Dexterity Under Dual Task in Parkinson's Disease
The Contribution of the Dual Task Interference on the Dexterity Related Activities of Daily Living in Parkinson's Disease
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Altinordu
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Ordu, Altinordu, Turkey, 52100
- Sevim ACARÖZ CANDAN
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diagnosis of idiopathic Parkinson's disease according to the criteria of the United Kingdom brain Bank by neurologist
- Age 50-90 range
- having sufficient cognitive status according to the Mini Mental Status Evaluation (24 or above from the Mini Mental Test)
Exclusion Criteria:
- Having orthopedic and neurological disorders affecting hand function,
- Having sensory problems,
- Having Diabetus mellitus
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Study Group
patients with parkinson disease
|
The nine hole peg test will be performed under two different task (1)single task, (2)adding a cognitive task
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Nine hole peg test
Time Frame: 5 minutes
|
The Nine-Hole Peg Test is used to measure finger dexterity in patients with various neurological diagnoses. The patient must pick up the pegs from the holes and replace them back as fast as possible. The Nine Hole Peg Test should be conducted with the dominant arm first, then nondominant hand. The time will be recorded in second to complete the test. The test will be performed under three task;
|
5 minutes
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ADL-related dexterity Questionnaire 24 (DextQ-24)
Time Frame: 10 minutes
|
Dexterity-related ADL difficulties were measured by the ADL-related dexterity Questionnaire 24 (DextQ-24), including 24 question dealing with bimanual and unimanual activities, which is a reliable and valid disease specific questionnaire to evaluate dexterity in patients with PD.
Each question is scored between 1 (no problems) and 4 (need aid to perform task) by the patient's experience.
Total score ranged from 24 points to 96 points.
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10 minutes
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Unified Parkinson's Disease Rating Scale (UPDRS) - Section of Activities of Daily Living (ADL)
Time Frame: 10 minutes
|
The UPDRS- ADL section evaluates the impact of Parkinson disease on ADL according to patient's perspective.
The ADL section consists of 13 items for gathering information on the patient's own perception of functional impairment due to PD.
Each item scores between 0-4.
0 means normal and 4 means severe impairment.
The total score change between 0-52.
High scores indicate severe impairment.
|
10 minutes
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Modified Hoehn and Yahr Scale
Time Frame: 2 minutes
|
Disease progression will be assessed with modified Hoehn and Yahr Scale. The original scale included stages 1 through 5. Since then, stage 0 has been added, and stages 1.5 and 2.5 have been proposed. This modified scale allocates stages from 0 to 5 to indicate the relative level of disability. Stage 0: No signs of disease. Stage 1: Unilateral symptoms only. Stage 1.5: Unilateral and axial involvement. Stage 2: Bilateral symptoms. No impairment of balance. Stage 2.5: Mild bilateral disease with recovery on pull test. Stage 3: Balance impairment. Mild to moderate disease. Physically independent. Stage 4: Severe disability, but still able to walk or stand unassisted. Stage 5: Needing a wheelchair or bedridden unless assisted. |
2 minutes
|
Unified Parkinson's Disease Rating Scale (UPDRS) - Motor Section
Time Frame: 10 minutes
|
Motor section of UPDRS determines the impairment due to the Parkinson's disease.
Rigidity, bradykinesia and tremor items which are relating with upper extremity function will be assessed.
Each item scores between 0-4.
0 means normal and 4 means severe impairment.
The total scores of rigidity, bradykinesia, and tremor, respectively range between 0-8, 0-24 and 0-16.
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10 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: SEVİM ACARÖZ CANDAN, Ordu University, Department of Physiotherapy and Rehabilitation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
- OrduU3
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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