Variability of Healthy People and People After Stroke Results in the Nine Hole Peg Test

March 24, 2026 updated by: Kateřina Rybářová, Charles University, Czech Republic
Main aim of the study is to find out how many attempts of each subtest in the Nine Hole Peg Test should be done in clinical practice during testing people after stroke who are 20-64 years old.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Czechia
      • Kladruby, Czechia
        • Rehabilitační ústav Kladruby
      • Prague, Czechia
        • Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Czech healthy people and Czech people after stroke

Description

Inclusion Criteria:

  • age: 20-64 years (inclusive)
  • hospitalized patient in Rehabilitation Centre Kladruby
  • women and men with Czech as their mother tongue
  • signed Informed consent
  • ability to maintain a stable sitting position for the duration necessary for testing
  • comprehension of verbal instructions and recordings for the Nine Hole Peg Test

Exclusion Criteria:

  • inability to successfully complete a pilot attempt of the Nine Hole Peg Test using the right and left hand
  • severe spastic paresis of the upper limb, which would make the test impossible
  • plegia of the upper limb
  • failure to complete the test to visual or hearing impairment
  • inability to understand verbal instructions
  • inability to maintain attention during testing
  • severe attention deficit disorder
  • neglect syndrome
  • fatigue
  • external factors that prevent the complete completion of the test

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
People after stroke
Czech people after stroke, aged 20 - 64 years
Diagnostic test: Nine Hole Peg Test
3 attempts of each subtest of the Nine Hole Peg Test performed according to the Czech Extended Version of Manual for the Nine Hole Peg Test; questionnaire
Other Names:
  • questionnaire
Healthy population
Czech healthy people, aged 20 - 64 years
Diagnostic test: Nine Hole Peg Test
3 attempts of each subtest of the Nine Hole Peg Test performed according to the Czech Extended Version of Manual for the Nine Hole Peg Test; questionnaire
Other Names:
  • questionnaire

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
results from the Nine Hole Peg Test
Time Frame: 30 minutes
time
30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Charles University, Czech Republic

Investigators

  • Principal Investigator: Kateřina Rybářová, Mgr., Charles University, Czech Republic

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 6, 2023

Primary Completion (Actual)

December 19, 2023

Study Completion (Actual)

December 30, 2023

Study Registration Dates

First Submitted

April 29, 2024

First Submitted That Met QC Criteria

April 29, 2024

First Posted (Actual)

May 2, 2024

Study Record Updates

Last Update Posted (Actual)

March 27, 2026

Last Update Submitted That Met QC Criteria

March 24, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 23/4

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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