ClinicalTrials.gg
CompletedNCT07887776Updated Oct 21, 2026

Physical Performance and Cognitive Functions in Patients With Chronic Stroke

An observational study in Stroke, sponsored by Kutahya Health Sciences University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Kutahya Health Sciences University · Observational

Updated Oct 21, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
66
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This study aims to investigate the impact of cognitive impairment on upper extremity physical performance, cognitive skills, and functional independence in individuals with chronic stroke. A total of 66 chronic stroke survivors will be enrolled and categorized into two groups based on their Montreal Cognitive Assessment (MoCA) scores: the Cognitive Impairment Group (n=33) and the Control Group (n=33). Upper extremity performance, cognitive functions, and functional independence will be comprehensively evaluated using standardized clinical outcome measures.

Read the detailed description

Background and Rationale:

Cognitive impairment is a frequent and disabling consequence of stroke that can significantly hinder motor recovery, physical performance, and independence in activities of daily living. Although physical rehabilitation predominantly focuses on motor functions, the intricate relationship between cognitive status and upper extremity performance warrants deeper investigation.

Objective:

To examine the effects of cognitive impairment on upper extremity physical performance, specific cognitive domains (attention and working memory), and functional independence in individuals with chronic stroke.

Study Design and Participants:

This cross-sectional comparative study will include 66 volunteer participants with chronic stroke. Participants will be divided into two equal groups (n=33 each) based on a cutoff threshold of the Montreal Cognitive Assessment (MoCA): a Cognitive Impairment Group and a Control Group. Both groups will be matched for age, stroke duration, sex, education level, and affected stroke side.

Assessments \& Outcome Measures:

Upper Extremity Physical Performance: Evaluated using the Wolf Motor Function Test (WMFT), Fugl-Meyer Upper Extremity Assessment (FM-UE), and the Box and Block Test (BBT).

Cognitive Skills: Evaluated using the Stroop Test, Forward Digit Span Test, and Backward Digit Span Test to assess executive functions, attention, and working memory.

Functional Independence: Evaluated using the Functional Independence Measure (FIM), separating motor and cognitive sub-scores.

Significance:

The findings of this study are expected to highlight the critical interaction between cognitive status and upper extremity motor performance in chronic stroke. Consequently, the results will emphasize the necessity of integrating routine cognitive assessments into standard clinical protocols and tailoring stroke rehabilitation programs to address patients' cognitive profiles.

02

Conditions studied

  • Stroke

Keywords

  • Cronic stroke
  • cognitive impairment
  • upper extremity
  • motor performance
  • functional independence
03

In context

Stroke

7,441 studies on the registry are indexed under Stroke; 2,012 are open to participants now.

This study's enrollment of 66 is below the median of 160 across 1,729 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Kutahya Health Sciences University is the lead sponsor of 216 studies on the registry; 49 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population comprises adult patients of both genders, aged between 18 and 80 years, who have experienced a single ischemic or hemorrhagic stroke at least six months prior to enrollment (chronic stroke phase). Participants are recruited from outpatient physical therapy and rehabilitation clinics. Based on their cognitive screening using the Montreal Cognitive Assessment (MoCA), the study population is categorized into two comparative cohorts: a Cognitive Impairment Group and a Control Group. Eligible participants must be able to communicate effectively, be literate, and have no pre-existing cognitive disorders, severe medical comorbidities, or concurrent neurological/orthopedic conditions that could independently affect physical or cognitive performance.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • History of ischemic or hemorrhagic stroke diagnosed at least 6 months prior to the study,
  • First-ever stroke
  • Absence of communication or language disorders that would prevent understanding and cooperation
  • Ability to read and write
  • Not currently receiving psychotropic medication treatment
  • Willingness to participate and provision of signed informed consent

Exclusion criteria

Exclusion Criteria:

  • Having a chronic and severe medical condition (e.g., epilepsy, cerebral palsy)
  • Presence of any other concurrent orthopedic or neurological disease affecting physical or cognitive performance
  • History of recent surgery
  • History of any pre-existing condition affecting cognitive status (e.g., dementia, neurodegenerative diseases)
  • Complete loss of vision or hearing
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
66 participants (actual)
Patient registry
No

Groups and cohorts

  • Cognitive Impairment Group

    Scoring 20 or lower on the Montreal Cognitive Assessment (MoCA)

  • Control Group

    Scoring 21 or higher on the Montreal Cognitive Assessment (MoCA)

06

What researchers measure

Primary outcomes

  1. Wolf Motor Function Test (WMFT) Performance Time

    valuates upper extremity motor ability and functional performance through timed and functional tasks. WMFT performance time is measured in seconds, where longer durations indicate lower performance.

    Time frame: Baseline (Single assessment session)

  2. Fugl-Meyer Upper Extremity Assessment (FM-UE) Score

    Measures motor recovery, reflex activity, and movement coordination in the upper extremity. Scores range from 0 to 66, with higher scores indicating better motor function.

    Time frame: Baseline (Single assessment session)

  3. Box and Block Test (BBT) Score

    Assesses unilateral manual dexterity. It measures the number of blocks transported from one compartment to another within 60 seconds (evaluated separately for affected and unaffected upper extremities).

    Time frame: Baseline (Single assessment session)

  4. Functional Independence Measure (FIM) Motor and Cognitive Sub-scores

    Evaluates the level of independence in activities of daily living. It consists of motor and cognitive sub-scales, where higher scores reflect greater functional independence.

    Time frame: Baseline (Single assessment session)

Secondary outcomes

  1. Stroop Test Completion Times

    Measures cognitive flexibility, selective attention, and executive functions. Completion times are recorded in seconds, where longer durations indicate greater cognitive impairment.

    Time frame: Baseline (Single assessment session)

  2. Forward and Backward Digit Span Test Scores

    Evaluates attention, short-term memory, and working memory capacity. Scores are based on the maximum number of digits successfully repeated in forward and backward order

    Time frame: Baseline (Single assessment session)

07

Study locations

1 site
  • Doç. Dr. Mustafa Kalemli Tavsanli State Hospital
    Kütahya, Tavşanlı 43300, Turkey (Türkiye)
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2025 to primary completion in Jun 2026, 17 months.

Of 787 non-industry observational studies under Stroke, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 18 and three quarters within 101. This study's 17 months is below that.

Counting every sponsor, half of 833 studies reached it within 41 months; a quarter within 18 and three quarters within 92.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 15, 2026
First posted
Oct 21, 2026
StartActual
Jan 1, 2025
Primary completionActual
Jun 30, 2026
CompletionActual
Jul 1, 2026
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07887776
Responsible party
Ismail Okur (Assit. Prof., Kutahya Health Sciences University) — Principal investigator
First posted
Oct 21, 2026
Start date
Jan 1, 2025
Primary completion
Jun 30, 2026
Completion
Jul 1, 2026
Last update
Oct 21, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion