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This study aims to compare the effects of standard and dual-task-oriented hand-arm bimanual intensive training on cognitive performance, upper limb function, and coordination in post-stroke patients. Stroke often leads to impairments in motor and cognitive functions, limiting independence in daily activities. This randomized controlled trial will include adult stroke patients who will be assigned to two groups: one receiving standard training and the other receiving dual-task-oriented training. The interventions will be provided over eight weeks. Outcomes will be assessed using standardized tools for motor function, coordination, and cognition. The study seeks to determine whether combining cognitive and motor tasks leads to better rehabilitation outcomes compared to standard therapy alone.
Stroke is a leading cause of long-term disability, commonly resulting in deficits in upper limb function, coordination, and cognitive performance. These impairments significantly affect the ability to perform daily activities and reduce overall quality of life. Rehabilitation strategies that integrate both motor and cognitive components may enhance functional recovery and promote neuroplasticity.
Hand-Arm Bimanual Intensive Training (HABIT) is a task-specific, repetitive, and goal-oriented intervention designed to improve bilateral upper limb function through coordinated use of both hands. While standard HABIT has demonstrated effectiveness in improving motor outcomes, dual-task-oriented HABIT incorporates simultaneous cognitive demands, such as attention and problem-solving, to better simulate real-life functional activities.
This study is a randomized controlled trial designed to compare the effects of standard HABIT and dual-task-oriented HABIT on cognitive performance, upper limb motor function, and coordination among post-stroke patients. A total of 20 participants aged 40-70 years with mild to moderate upper limb impairment will be recruited. Participants will be randomly assigned to either the intervention group receiving a combination of standard and dual-task-oriented HABIT or the control group receiving standard HABIT only. The intervention will be delivered over eight weeks, with three sessions per week.
Outcome measures will include the Fugl-Meyer Assessment for upper limb function, Action Research Arm Test for functional performance, Finger-to-Nose test for coordination, and Montreal Cognitive Assessment for cognitive evaluation. Assessments will be conducted at baseline, mid-intervention (4 weeks), and post-intervention (8 weeks).
The findings of this study will provide evidence on whether integrating cognitive challenges into bimanual training leads to superior rehabilitation outcomes, supporting more comprehensive and functionally relevant stroke rehabilitation strategies.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Standard HABIT | Active Comparator | Participants will receive standard hand-arm bimanual intensive training for 8 weeks, with three sessions per week. |
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| Dual-Task-Oriented HABIT | Experimental | Participants will receive standard hand-arm bimanual intensive training for the first 4 weeks, followed by dual-task-oriented hand-arm bimanual intensive training for the remaining 4 weeks, with three sessions per week. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Standard HABIT | Behavioral | Participants will receive standard hand-arm bimanual intensive training for 8 weeks, with three sessions per week. |
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| Measure | Description | Time Frame |
|---|---|---|
| Upper Limb Motor Function | Upper limb motor function will be assessed using the Fugl-Meyer Assessment for Upper Extremity (FMA-UL), a validated scale evaluating motor recovery, movement control, and coordination in post-stroke patients. | Baseline, Week 4, and Week 8 |
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Inclusion Criteria:
Both male and female' genders.
Exclusion Criteria:
Severe cognitive impairment or expressive/receptive aphasia limiting effective communication. (10)
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| ambreen iqbal, phD | Contact | +923227616154 | iqbalambreen8@gmail.com | |
| Wajeeha zia, phD | Contact | +92323450078 | wajeeha.zia@riphah.edu.pk |
| Name | Affiliation | Role |
|---|---|---|
| Ambreen iqbal, phD | Riphah International University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sahara Hospital | Narowal | Punjab Province | Pakistan |
Individual participant data will not be shared. The data will be used solely for academic and research purposes and will remain confidential.
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| ID | Term |
|---|---|
| D020521 | Stroke |
| ID | Term |
|---|---|
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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participants will be assigned to one of two parallel groups: standard hand-arm bimanual intensive training or dual-task-oriented hand-arm bimanual intensive training.
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Outcome assessors will be blinded to group allocation. Due to the nature of the interventions, participants and care providers cannot be masked.
| Dual-Task-Oriented HABIT | Other | Participants will receive standard hand-arm bimanual intensive training for the first 4 weeks, followed by dual-task-oriented hand-arm bimanual intensive training for the remaining 4 weeks, with three sessions per week. |
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| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |