Turkish Parkinson's dementia test put under the microscope

NCT ID NCT07815964

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
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The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
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Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Sep 11, 2026 · Last updated Sep 15, 2026 · Updated 2 times

Summary

Researchers are checking whether a Turkish translation of the Parkinson Neuropsychometric Dementia Assessment (PANDA) gives consistent and accurate results in people with Parkinson's disease. About 100 Turkish-speaking patients will complete the questionnaire, which tests memory, verbal fluency, visuospatial skills, and delayed recall. A subgroup will take the test again later to see if scores stay stable over time. The goal is to provide doctors with a reliable tool for detecting cognitive decline in this population.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
the Turkish version of the Parkinson Neuropsychometric Dementia Assessment (PANDA), a cognitive screening questionnaire
What this could lead to
If the Turkish PANDA proves reliable, doctors could use it to spot thinking and memory problems in Turkish-speaking people with Parkinson's disease earlier and more accurately.
What could go wrong
This is a small, single-country validation study, so the results may not apply to other languages or populations. A screening questionnaire can flag possible cognitive issues but cannot diagnose dementia on its own.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population will consist of individuals with clinically diagnosed Parkinson's disease (Hoehn and Yahr stage 1-3), aged between 40 and 85 years, with adequate cognitive function (MMSE ≥ 24). Participants will be recruited from patients attending the Movement Disorders Outpatient Clinic of the Neurology Department. The study population represents ambulatory individuals with mild to moderate disease severity suitable for comprehensive biopsychosocial assessment.

Ages

40 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

\*\*Inclusion Criteria:\*\* * Clinical diagnosis of Parkinson's disease * Hoehn and Yahr stage 1-3 * Age between 40 and 85 years * Mini-Mental State Examination score ≥ 24 * Sufficient cognitive and communication ability to complete the assessments * Attendance at the Movement Disorders Outpatient Clinic of the Neurology Department * Willingness to participate in the study and provide written informed consent \*\*Exclusion Criteria:\*\* * Presence of a major psychiatric disorder, such as major depressive disorder or a psychotic disorder * Diagnosis of advanced dementia * Presence of an uncontrolled systemic chronic disease, such as uncontrolled diabetes mellitus or hypertension * Presence of a severe cardiovascular or respiratory condition * Presence of an additional orthopedic or neurological condition that may affect assessment performance * Severe visual or hearing impairment that may interfere with the assessments * Inability to cooperate adequately during the assessments

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

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  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • Acibadem University

    Istanbul, Turkey, +90, Turkey (Türkiye)

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