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Motor ActivityNCT05009108

Establishing of the Reliability of the Purdue Pegboard Test in Adults After a Stroke

An observational study of Motor Activity, run by Charles University, Czech Republic at 2 sites in Czechia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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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. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Motor Activity
What is being tested?
Purdue Pegboard Test
How many people
31 participants
Where
2 sitesCzechia
Study dates
16 Jul 2021to 30 Dec 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Czech adult patients after a stroke

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

2 sites in 1 country.

Czechia2 sites
  • Rehabilitační ústav Kladruby

    Kladruby

  • Department of Rehabilitation Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague

    Prague

Other trials in Czechia

About this study

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.

Read the detailed 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.

Conditions
Motor Activity
Being tested
Purdue Pegboard Test
Keywords
Standardized test, Occupational therapy, Fine motor skills, Purdue Pegboard Test, Czech language, Inter-rater reliability, Internal variability, Stroke, Adults
Medical subject headings
Motor Activity, Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Purdue Pegboard TestDiagnostic test

    Also called questionnaire

    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.

Study groups in NCT05009108
Study groupRoleWhat they receive
Czech adult patients after a strokeCzech adults patients after a stroke will be asked to fill in a informed agreement and as well to answer short questionnaire. Then they will be tested by the Purdue Pegboard Test in only one session. Video of their performance will be obtained as well.
Receives: Diagnostic Test: Purdue Pegboard Test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. results from the Purdue Pegboard Test

    number of parts put in the Pegboard according to the rules

    Measured: 25 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Aug 2021
  2. Study start16 Jul 2021
  3. Primary completion21 Oct 2022
  4. Study completion30 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
31 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05009108
Sponsor's protocol ID
21/05/2021
Status last verified
Apr 2024
First submitted
12 Aug 2021
Last updated
30 Apr 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Motor Activity, run by Charles University, Czech Republic at 2 sites in Czechia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 30 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

results from the Purdue Pegboard Test (time frame: 25 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2024.

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