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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05009108
Other study ID # 21/05/2021
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 16, 2021
Est. completion date December 30, 2024

Study information

Verified date April 2024
Source Charles University, Czech Republic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main aim of the pilot project is to establish inter-rater reliability, internal variability and variability of results got by testing adults patients after a stroke by the use of Purdue Pegboard Test administered according to the new Czech extended version of its manual.


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 31
Est. completion date December 30, 2024
Est. primary completion date October 21, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Purdue Pegboard Test
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.

Locations

Country Name City State
Czechia Rehabilitacní ústav Kladruby Kladruby
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 Purdue Pegboard Test number of parts put in the Pegboard according to the rules 25 minutes
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