Establishing Czech Norms of Selected Standardized Tests

February 14, 2024 updated by: Kateřina Rybářová, Charles University, Czech Republic

Establishing Czech Norms of Selected Standardized Tests for Use in Rehabilitation and Upper Limbs Functional Evaluation

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.

Study Overview

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

Observational

Enrollment (Estimated)

540

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

Study Locations

      • Praha, Czechia
        • Recruiting
        • Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
        • 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

20 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Czech healthy men and women

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

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

  • 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

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

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)

October 18, 2021

Primary Completion (Estimated)

October 31, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

August 12, 2021

First Submitted That Met QC Criteria

August 12, 2021

First Posted (Actual)

August 18, 2021

Study Record Updates

Last Update Posted (Estimated)

February 15, 2024

Last Update Submitted That Met QC Criteria

February 14, 2024

Last Verified

February 1, 2024

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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