Variability of Healthy People and People After Stroke Results in the Box and Block Test

Sponsor
Charles University, Czech Republic (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05925231
Collaborator
(none)
60
1
13
4.6

Study Details

Study Description

Brief Summary

Main aim of the study is to find out how many attempts of each subtest in the Box and Block Test should be done in clinical practice during testing people after stroke who are 20-64 years old.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Box and Block Test

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Variability of Healthy People and People After Stroke Results in the Box and Block Test
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
May 30, 2024
Anticipated Study Completion Date :
Jul 31, 2024

Arms and Interventions

Arm Intervention/Treatment
People after stroke

Czech people after stroke, aged 20 - 64 years

Diagnostic Test: Box and Block Test
3 attempts of each subtest of the Box and Block Test performed according to the Czech Extended Version of Manual for the Box and Block Test
Other Names:
  • questionnaire
  • Healthy population

    Czech healthy people, aged 20 - 64 years

    Diagnostic Test: Box and Block Test
    3 attempts of each subtest of the Box and Block Test performed according to the Czech Extended Version of Manual for the Box and Block Test
    Other Names:
  • questionnaire
  • Outcome Measures

    Primary Outcome Measures

    1. results from the Box and Block Test [30 minutes]

      number of transported blocks

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 64 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • people after stroke 20 - 64 years old

    • signed 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

    • ability to sit independently for 15 minutes

    • ability to grasp and move at least one 25 mm wide cube placed on a table using the dominant and then the non-dominant upper limb across the test partition

    • ability to perform a simple task following verbal instructions

    • retained ability to understand - according to psychological examination

    • completion of testing during hospitalization in the Beroun Rehabilitation Hospital

    Exclusion Criteria:
    • severe hearing impairment not corrected by a hearing aid

    • severe visual impairment not corrected by glasses

    • severe comprehension impairment

    • other reasons not allowing the completion of the entire testing using the Box and Block Test

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rehabilitation Hospital of Beroun Beroun Czechia

    Sponsors and Collaborators

    • Charles University, Czech Republic

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kateřina Rybářová, Occupational therapist, Charles University, Czech Republic
    ClinicalTrials.gov Identifier:
    NCT05925231
    Other Study ID Numbers:
    • 75/23 S-IV
    First Posted:
    Jun 29, 2023
    Last Update Posted:
    Jul 3, 2023
    Last Verified:
    Jun 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Kateřina Rybářová, Occupational therapist, Charles University, Czech Republic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 3, 2023