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NCT05009121 Clinical Trial

The Reliability of the Box and Block Test in People After Stroke

Motor Activity Clinical Trial

Official title:
The Reliability of the Box and Block Test in People After Stroke

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05009121
Other study ID # 75/21 S-IV
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 31, 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 in Box and Block Test administered according to the new Czech extended version of its manual.

Description:

New Czech manual for the Box and Block Test was made by back-translation method. It was updated and extended by new rules for unification of it´s performing. The manual include instructions for performing three trials. At least 20 adult people after stroke will be tested by this test according to this new Czech manual. Video of patients' performance will be obtained. The inter-rater reliability, internal variability and variability of results will be established.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 20
Est. completion date December 30, 2024
Est. primary completion date February 28, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Czech language as a mother tongue - Adult (age 18 and more) - Patient after Stroke attending the Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague - Able to move 25mm X 25mm block at least by 10 cm - Able to complete testing with full 3 attempts - Able to sit for 20 minutes Exclusion Criteria: - use of drugs affecting attention - vision impairment uncorrectable with glasses - severe hearing loss - inability to understand instructions - 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:
• Box and Block Test
At first, each person will be asked basic questions about present feelings according to their condition using a questionnaire. Than he/she will be tested by the Box and Block Test according to the Czech version of extended manual for this test in only one session. Audio recording of verbal instructions will be used. The results will be used only for establishing of the variability and inter-rater reliability of the Box and Block Test, not for patients' other interventions.

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 Box and Block Test number of transported blocks 30 minutes
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