- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05009108
Establishing of the Reliability of the Purdue Pegboard Test in Adults After a Stroke
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
New Czech manual for the Purdue Pegboard Test which is updated and extended by new rules for unification of their performing will be used for testing adult people with disability - adults after a stroke. The manuals include instructions for performing three trials of each subtest.
At least 30 adult patients after a stroke will be tested by use of Purdue Pegboard test administrated according to the new Czech extended version of its manual. Video of performance of each adult will be obtained. Performance of each patient, firstly in real time and secondly from video record will be evaluated twice, to obtain result for establishing all types of variability and reliability mentioned below.
The inter-rater reliability, internal variability and variability of results will be established.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Kladruby, Czechia
- Rehabilitační ústav Kladruby
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Praha, Czechia
- Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Czech language as a mother tongue
- age from 18 to 65 years
- patient after a stroke hospitalized at Rehabilitation institute Kladruby
- fine motor skills allowing them correct manipulation with components of Purdue Pegboard Test
Exclusion Criteria:
- severe disorder of orientation (neglect syndrome)
- use of drugs affecting attention
- vision impairment uncorrectable with glasses
- severe hearing loss
- inability to understand instructions
- inability to read or write
- inability to complete complete testing due to severe spasticity or spastic dystonia
- failure to sign Informed consent for probation with inclusion to research and Consent to the collection and processing of personal data during the study at the Rehabilitation institute Kladruby
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Czech adult patients after a stroke
Czech adults patients after a stroke will be asked to fill in a informed agreement and as well to answer short questionnaire.
Then they will be tested by the Purdue Pegboard Test in only one session.
Video of their performance will be obtained as well.
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At first, each person will be asked to fill in the informed agreement and answer short questionnaire. Than he/she will be tested by the Purdue Pegboard Test according to the Czech version of extended manuals for those tests in only one session. Audio recording of verbal instructions will be used and whole testing process will be video recorded which is necessary for establishing the internal variability and variability of results of the Purdue Pegboard Test. The results will be used only for establishing of the variability and inter-rater reliability of the Purdue Pegboard Test, not for patients' other interventions.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
results from the Purdue Pegboard Test
Time Frame: 25 minutes
|
number of parts put in the Pegboard according to the rules
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25 minutes
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21/05/2021
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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