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RecruitingNCT05925231Updated Apr 30, 2024

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

An observational study in Motor Activity, sponsored by Charles University, Czech Republic. Recruiting at 2 sites in Czechia. Open to participants aged 20 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-04-30.

Sponsored by Charles University, Czech Republic · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2024, 2 years ago, but the record still lists the study as recruiting.
  • Started Jul 2023; still recruiting 3 years 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
20 Years to 64 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Motor Activity

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Keywords

  • Box and Block Test
  • Stroke
  • Czech Extended Version of Manual for the Box and Block Test
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 60 is below the median of 160 across 1,692 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Charles University, Czech Republic is the lead sponsor of 220 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

People after stroke, healthy people

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

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
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • People after stroke

    Czech people after stroke, aged 20 - 64 years

    Diagnostic Test: Box and Block Test

  • Healthy population

    Czech healthy people, aged 20 - 64 years

    Diagnostic Test: Box and Block Test

Interventions

  • Diagnostic testBox 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

    Also known as: questionnaire

06

What researchers measure

Primary outcomes

  1. results from the Box and Block Test

    number of transported blocks

    Time frame: 30 minutes

07

Study locations

2 of 2 sites recruiting
  • Rehabilitation Hospital of Beroun
    Beroun, Czechia
    Recruiting
  • Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
    Praha, Czechia
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05925231
Lead sponsor
Charles University, Czech Republic
Responsible party
Kateřina Rybářová (Occupational therapist, Charles University, Czech Republic) — Principal investigator
First posted
Jun 29, 2023
Start date
Jul 1, 2023
Primary completion
Sep 30, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Apr 30, 2024

Study contacts

Kateřina Rybářová, Mgr.
Contact
katerina.rybarova@lf1.cuni.cz
224968517

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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