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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05661617
Other study ID # 219/22 S-IV
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 19, 2023
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source Charles University, Czech Republic
Contact Katerina Rybárová, Mgr.
Phone 224968517
Email katerina.rybarova@lf1.cuni.cz
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the research study is to find out how the results of healthy women aged 20-24 years (inclusive) differ in the Nine Peg Test, the Purdue Pegboard Test and the Box and Block Test, depending on the laterality of the research participants and the order of the performed subtests of the investigated tests. In this way, it will be preliminarily determined whether it is necessary to create normative data separately for right-handed and left-handed people for the tests.


Description:

Research participants will be tested in one meeting after giving informed consent, answering a few short questions regarding health status and filling out a short questionnaire using the Czech extended version of the manual for all three standardized tests, and always according to a predetermined order. Intentionally, all research participants with a dominant right upper limb will be tested as if they were left-handed, and vice versa. The results of the research participants tested in this way will be compared with the results of women from the same age category who have already been properly tested as part of an ongoing research study entitled: "Establishing Czech Norms of Selected Standardized Tests".


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2024
Est. primary completion date October 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 24 Years
Eligibility Inclusion Criteria: - Czech language as a mother tongue - age from 20 to 24 years (inclusive) - female 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Nine Hole Peg Test, Purdue Pegboard Test, Box and Block Test
Research participants were tested in one meeting after giving informed consent, answering a few short questions regarding health status and filling out a short questionnaire using the Czech extended version of the manual for the Nine Hole Peg Test, Purdue Pegboard Test and Box and Block Test, and always according to a predetermined order. Intentionally, all research participants from experimental group with a dominant right upper limb will be tested as if they were left-handed, and vice versa. All research participants from normative study were tested normally according to the Czech extended manuals for those tests.

Locations

Country Name City State
Czechia Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague Praha

Sponsors (1)

Lead Sponsor Collaborator
Charles University, Czech Republic

Country where clinical trial is conducted

Czechia, 

Outcome

Type Measure Description Time frame Safety issue
Primary results from the Nine Hole Peg Test time in seconds and hundreds of seconds 10 minutes
Primary results from the Purdue Pegboard Test number of parts put in the Pegboard according to the rules 25 minutes
Primary results from the Box and Block Test number of transported blocks 30 minutes
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