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).
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
- Type of treatment
- Lifestyle or therapy programme
- 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
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.
- Conditions
- Stroke Rehabilitation
- 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 group | Role | What they receive |
|---|---|---|
| Conventional Rehabilitation Group | Active comparator | Participants 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 1 | Experimental | Participants 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 2 | Experimental | Participants 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.
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)
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)
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.
- First posted4 May 2026
- Study start1 May 2026
- Primary completion20 Nov 2026 (estimated)
- Study completion20 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Stroke RehabilitationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Motor Imagery on Upper Extremity Function in Stroke Rehabilitation: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07565363
- Acronym / sponsor ID
- MI-STROKE-UE-2026
- Conditions
- Stroke Rehabilitation
- Keywords
- Motor Imagery (MI), Upper Extremity, Stroke, Rehabilitation
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 51 participants (estimated)
- Lead sponsor
- Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research HospitalUniversity, hospital or other
- Study start
- 1 May 2026 (actual)
- Primary completion
- 20 Nov 2026 (estimated)
- Study completion
- 20 Dec 2026 (estimated)
- First posted
- 4 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Conventional Rehabilitation Group | Active comparator | Behavioral: Conventional RehabilitationParticipants 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. |
| Motor Imagery + Conventional Rehabilitation Group 1 | Experimental | Behavioral: Motor Imagery Training 1Participants will receive, in addition to conventional rehabilitation, 15 minutes of motor imagery training three days per week. |
| Motor Imagery + Conventional Rehabilitation Group 2 | Experimental | Behavioral: Motor Imagery Training 2Participants will receive, in addition to conventional rehabilitation, 15 minutes of motor imagery training five days per week. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Conventional RehabilitationAlso: controlA physiotherapy program comprising range of motion exercises, stretching, strengthening exercises, neuromuscular facilitation techniques, and neurophysiological approaches such as Brunnstrom and Bobath. | Behavioural | Conventional Rehabilitation Group |
| Motor Imagery Training 1A 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. | Behavioural | Motor Imagery + Conventional Rehabilitation Group 1 |
| Motor Imagery Training 2A 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. | Behavioural | Motor Imagery + Conventional Rehabilitation Group 2 |
Primary outcome
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)
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
2 secondary outcomes
Change in the Modified Barthel Index (MBI) score from baseline assessment.
Time frame: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)
Change in the Wolf Motor Function Test (WMFT) score from baseline assessment
Time frame: Baseline, at 6 weeks (end of intervention), and at 12 weeks (follow-up)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.