- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05010993
Establishing Czech Norms of Selected Standardized Tests
Establishing Czech Norms of Selected Standardized Tests for Use in Rehabilitation and Upper Limbs Functional Evaluation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The main aim of the project is to establish Czech updated manuals for the Nine Hole Peg Test, Purdue Pegboard Test and Box and Block Test to be used in rehabilitation to evaluate upper limb functions, including establishing norms for the Czech healthy population.
The Czech updated manuals for those tests were made by back-translation method and updated for unification of recommended three trials of each subtest administration and interpretation of tested individuals performance.
At least 540 individuals (20-65 years old) will be tested by the updated Czech manuals till the end of 2023 by those three tests. The Czech norms will be established from acquired data.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Kateřina Rybářová, Mgr.
- Phone Number: 224968517
- Email: katerina.rybarova@lf1.cuni.cz
Study Locations
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-
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Praha, Czechia
- Recruiting
- Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
-
Contact:
- Kateřina Rybářová, Mgr.
- Phone Number: 224968517
- Email: katerina.rybarova@lf1.cuni.cz
-
-
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 20 to 65 years
Exclusion Criteria:
- diagnosed pathology of the upper limbs or diseases that negatively affect the dexterity of their limbs
- 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 testing
- 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 General University Hospital in Prague
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Czech healthy people
Czech healthy men and women will be asked to fill in a questionnaire.
Then they will be tested by the Nine Hole Peg Test, the Purdue Pegboard Test and the Box and Block Test.
|
Each person will be tested by the Nine Hole Peg Test (3 attempts per subtest)
Each person will be tested by the Purdue Pegboard Test (3 attempts per subtest)
Each person will be tested by the Box and Block Test (3 attempts per subtest)
|
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
|
25 minutes
|
|
results from the Nine Hole Peg Test
Time Frame: 10 minutes
|
time in seconds and hundreds of seconds
|
10 minutes
|
|
results from the Box and Block Test
Time Frame: 30 minutes
|
number of transported blocks
|
30 minutes
|
Collaborators and Investigators
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 (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- EK-1340.14/20
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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