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Stroke RehabilitationNCT07565363

The Effect of Motor Imagery on Upper Extremity Function in Stroke Rehabilitation

A study testing Conventional Rehabilitation, Motor Imagery Training 1 and Motor Imagery Training 2 in people with Stroke Rehabilitation, run by Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Stroke is one of the leading causes of mortality and disability worldwide. A proportion of individuals who experience a stroke fail to achieve the desired level of motor recovery in the affected upper extremity following rehabilitation, resulting in significant limitations in activities of daily living. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Stroke Rehabilitation
What is being tested?
Conventional Rehabilitation, Motor Imagery Training 1 and Motor Imagery Training 2
Could I receive a placebo?
No, everyone receives an active treatment
How many people
51 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 May 2026to 20 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Being aged 18 years or older
  • Having a diagnosis of ischemic or hemorrhagic stroke confirmed by computed tomography (CT) or magnetic resonance imaging (MRI)
  • Being in the late subacute phase (more than 3 months post-stroke) or chronic phase (more than 6 months post-stroke) following stroke onset
  • Presence of unilateral extremity hemiparesis
  • Upper extremity stage between II and V for both proximal and distal segments according to the Modified Brunnstrom Classification
  • A score of 21 or higher on the Mini-Mental State Examination (MMSE)

Who cannot join

  • Severe spasticity in the affected upper extremity, defined as a Modified Ashworth Scale score > 2
  • Presence of impaired consciousness, or severe hearing, visual impairment or global aphasia.
  • Musculoskeletal disorders affecting upper extremity motor function, such as fracture or arthritis in the affected upper limb

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital

    Istanbul, Istanbul, 34785

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Motor Imagery on Upper Extremity Function in Stroke Rehabilitation: A Randomized Controlled Trial

Stroke is one of the leading causes of mortality and disability worldwide. A proportion of individuals who experience a stroke fail to achieve the desired level of motor recovery in the affected upper extremity following rehabilitation, resulting in significant limitations in activities of daily living. After stroke, rehabilitation programs are essential to reduce disability and enhance functional outcomes.

This study aims to evaluate whether the addition of Motor Imagery (MI) to a standard rehabilitation program contributes to improvements in upper extremity motor function in individuals with stroke. MI is a mental practice technique in which individuals cognitively rehearse movements without physically performing them. Although the movement is not executed, the brain regions involved in the movement are activated.

Read more

Eligible participants will be randomly assigned to three groups. All groups will receive a standard physical therapy and rehabilitation program. The first group will receive only standard physical therapy and rehabilitation. The second group will receive, in addition to conventional therapy, 15 minutes of MI training three days per week, while the third group will receive 15 minutes of MI training five days per week. The total treatment duration for all groups is planned as 30 sessions.

Assessments will be conducted at baseline, at the end of the treatment period, and again at the 12th week. This study is based on the hypothesis that adding MI practice to a conventional upper extremity rehabilitation program after stroke will contribute to improvements in activities of daily living and functional recovery, and that these effects may be associated with the frequency of the intervention.

Read the detailed description

Stroke is defined by the World Health Organization as a clinical syndrome characterized by focal or generalized neurological impairment of cerebrovascular origin lasting longer than 24 hours or resulting in death. Stroke is one of the leading causes of mortality and disability worldwide. Approximately 30% to 66% of individuals who experience a stroke fail to achieve satisfactory motor recovery in the affected upper extremity following rehabilitation; this condition constitutes a major source of disability and leads to substantial limitations in activities of daily living.

The majority of functional recovery is achieved within the first three months after onset. In the chronic phase, functional recovery is slower; however, neuroplastic changes continue to occur during this period. Following stroke, rehabilitation programs are essential to reduce disability. Upper extremity rehabilitation after stroke commonly includes range of motion exercises, stretching, strengthening exercises, neuromuscular facilitation techniques, neurophysiological approaches such as Brunnstrom and Bobath, and functional electrical stimulation.

Motor imagery (MI) and mental practice can be defined as continuous processes in which an individual attempts to simulate a movement using cognitive processes without physically performing the motor action. In other words, MI consists of the mental representation of a movement that is not actually executed. Through this process, it is aimed to acquire and optimize motor skills by generating a voluntary neural drive. MI does not require substantial economic investment and can be performed in any setting, as it does not necessitate specialized equipment. It is also considered safe, as it can be repeated multiple times without requiring significant physical effort.

In the existing literature, there is no clear consensus regarding the optimal duration and frequency of treatment. Although some authors suggest that the number of weekly treatment sessions and repetitions may influence motor learning, our review did not identify studies specifically addressing this issue.

Considering these factors, the present study aims to investigate the effects of MI on upper extremity motor function in individuals with stroke during the late subacute and chronic phases, and to determine whether these effects are associated with the frequency of the applied intervention. For this purpose, participants will be divided into three groups.

All groups will receive a routine conventional physical therapy and rehabilitation program in accordance with the clinical practice guidelines of the Turkish Society of Physical Medicine and Rehabilitation. The first group will receive only the routine conventional physical therapy and rehabilitation program. The second group will receive, in addition to conventional therapy, 15 minutes of MI training three days per week, while the third group will receive 15 minutes of MI training five days per week. The treatment program for all groups is planned as 30 sessions, each lasting 60 minutes.

For the MI intervention, a goal-oriented video recording will be prepared, including visually and auditorily guided representations of activities of daily living. These will include elbow flexion and extension, wrist flexion and extension, forearm pronation and supination, hand opening and closing, finger walking, thumb-to-finger opposition (touching the tip of each finger sequentially), reaching for an object, grasping and lifting it, drinking water from a bottle, combing hair, and opening a door handle. This video will be used as a supportive tool during MI training.

The motor imagery intervention will be conducted in a quiet room under the supervision of a physiotherapist and will follow the procedure below: the session will begin with whole-body relaxation. The participant will then watch the video depicting the target movement. Afterwards, the participant will be asked to close their eyes and imagine themselves performing the movement. The session will end with a return to a relaxed bodily state. This cycle will be repeated five times for each movement. During the procedure, participants will be instructed to focus on themselves and to avoid excessive stress and anxiety.

Assessments will be conducted at baseline, at the end of the treatment period, and at the 12th week.

Being tested
Conventional Rehabilitation, Motor Imagery Training 1, Motor Imagery Training 2
Keywords
Motor Imagery (MI), Upper Extremity, Stroke, Rehabilitation
Medical subject headings
Stroke

What participants receive

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

  • Conventional RehabilitationBehavioural

    Also called control

    A physiotherapy program comprising range of motion exercises, stretching, strengthening exercises, neuromuscular facilitation techniques, and neurophysiological approaches such as Brunnstrom and Bobath.

  • Motor Imagery Training 1Behavioural

    A structured motor imagery program, applied in addition to conventional rehabilitation, consisting of visual and kinesthetic mental rehearsal of functional movements, delivered for 15 minutes per session, three days per week.

  • Motor Imagery Training 2Behavioural

    A structured motor imagery program, applied in addition to conventional rehabilitation, consisting of visual and kinesthetic mental rehearsal of functional movements, delivered for 15 minutes per session, five days per week.

Study groups in NCT07565363
Study groupRoleWhat they receive
Conventional Rehabilitation GroupActive comparatorParticipants will receive a structured, conventional rehabilitation program consisting of range of motion exercises, stretching, strengthening exercises, neuromuscular facilitation techniques, and neurophysiological approaches such as Brunnstrom and Bobath.
Receives: Behavioral: Conventional Rehabilitation
Motor Imagery + Conventional Rehabilitation Group 1ExperimentalParticipants will receive, in addition to conventional rehabilitation, 15 minutes of motor imagery training three days per week.
Receives: Behavioral: Motor Imagery Training 1
Motor Imagery + Conventional Rehabilitation Group 2ExperimentalParticipants will receive, in addition to conventional rehabilitation, 15 minutes of motor imagery training five days per week.
Receives: Behavioral: Motor Imagery Training 2

What is being measured

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

  1. Change in the Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score from baseline assessment

    The Fugl-Meyer Assessment for Upper Extremity (FMA-UE) is a stroke-specific, performance-based impairment index designed to assess motor function of the upper extremity. The scale evaluates movement, coordination, and reflex activity of the shoulder, elbow, forearm, wrist, and hand. Scores range from 0 to 66, with higher scores indicating better motor function

    Measured: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)

Secondary outcomes (2)
  1. Change in the Modified Barthel Index (MBI) score from baseline assessment.

    The Modified Barthel Index (MBI) is used to assess functional independence in activities of daily living (ADL), including feeding, bathing, grooming, dressing, toileting, transfers, mobility, and stair use. The total score ranges from 0 to 100, with higher scores indicating greater independence

    Measured: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)

  2. Change in the Wolf Motor Function Test (WMFT) score from baseline assessment

    The Wolf Motor Function Test (WMFT) is used to assess upper extremity motor ability through timed and functional tasks. It includes 15 tasks evaluating movement and object manipulation. Performance is measured by the time required to complete each task (in seconds) and a functional ability scale ranging from 0 to 5, where higher scores indicate better motor performance.

    Measured: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)

Timeline

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

  1. First posted4 May 2026
  2. Study start1 May 2026
  3. Primary completion20 Nov 2026 (estimated)
  4. Study completion20 Dec 2026 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
51 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07565363
Sponsor's protocol ID
MI-STROKE-UE-2026
Status last verified
Sep 2026
First submitted
27 Apr 2026
Last updated
22 Sep 2026
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?

A study testing Conventional Rehabilitation, Motor Imagery Training 1 and Motor Imagery Training 2 in people with Stroke Rehabilitation, run by Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital at 1 site in Turkey (Türkiye).

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 6 inclusion and 3 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: under way, not looking for participants, as of the sponsor's last update on 22 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). 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?

This study is still under way. Results are not available in the source record yet.

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?

Change in the Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score from baseline assessment (time frame: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)). 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 22 Sep 2026.

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