Comparative Study of Action Observation Training Versus Task Oriented Training on Reaching in Patients With Stroke
1 other identifier
interventional
39
1 country
1
Brief Summary
Stroke is characterized by a sudden onset of localized or generalized brain dysfunction, with symptoms persisting for at least 24 hours or resulting in death. In the chronic phase following a stroke, hand dysfunction is commonly observed, often characterized by reduced finger strength and abnormal hand flexion patterns. Reaching is a crucial aspect of daily tasks, including activities like drinking, interacting with a touch screen, or pressing elevator buttons.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable stroke
Started Jun 2025
Shorter than P25 for not_applicable stroke
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 5, 2025
CompletedFirst Submitted
Initial submission to the registry
August 20, 2025
CompletedFirst Posted
Study publicly available on registry
August 27, 2025
CompletedAugust 27, 2025
August 1, 2025
2 months
August 20, 2025
August 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Reaching Performance Scale for Stroke (RPSS)
Evaluates the performance of two reaching and grasping tasks
4 Weeks
Wolf Motor Function Test (WMFT)
Designed to assess upper limb motor function following stroke or traumatic brain injury
4 Weeks
Study Arms (3)
Group A
EXPERIMENTALGroup B
EXPERIMENTALGroup C
EXPERIMENTALInterventions
Passive stretching, active range of motion exercises, isometric strengthening, and functional gripping practice for the hand
Seated in chair with arm and back support, with forearms resting on a table 73 cm high. Functional movements were trained through task-oriented exercises involving simple activities of daily living(ADL), such as eating (using a plate and spoon), personal hygiene (combing hair, brushing teeth), and tasks using household items (e.g., handling a cup and spoon, or opening a bottle and cap). Each task was repeated five times. Patients were allowed rest periods of five minutes as needed during the exercise sessions.
sat comfortably in a chair or wheelchair with both arms resting on a table (73 cm high) positioned 50 cm from a 15.6-inch colored laptop screen. They were instructed to attentively observe action videos displayed on the screen and then imitate the observed movements using their affected upper limb. A total of 30 action videos were used, each lasting approximately 50 seconds and demonstrating specific upper limb movements, such as wrist flexion/extension, abduction/adduction, pronation/supination, ulnar/radial deviation, and various grasping and manipulation tasks (e.g., handling coins, pens, a computer mouse, jar lids, bottle caps, typewriting, dialing a phone, and feeding).
Eligibility Criteria
You may qualify if:
- Patients with Chronic stroke diagnosed and referred by a neurologist.
- Patient's ages ranged from 50-65 years old, Duration of stroke was between six to 12 months, Spasticity grade of the upper limb was from 1 to 1+ according to the modified Ashworth scale (MAS).
- Patients with sufficient cognitive abilities that enabled them to understand and follow instructions (Mini-Mental Scale\>24), Fugl-Meyer Assessment scale for upper limb scored between 38 and 63.
- Patients with normal vision and hearing, Medically stable patients.
You may not qualify if:
- Patients with Upper limb dysfunction due to neurological disorders other than Stroke (e.g, Multiple Sclerosis, Parkinsonism...etc).
- Patients with Severe sensory deficits in the paretic upper limb, Psychological or severe cognitive disorders, Severe cardiovascular disease that can preclude intervention.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ahmed Alshimylead
Study Sites (1)
Al Ryada University for Science and Technology
Sadat, Menoufia, 32897, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Lecturer of Physical Therapy for Neurology and it's Surgery
Study Record Dates
First Submitted
August 20, 2025
First Posted
August 27, 2025
Study Start
June 2, 2025
Primary Completion
July 25, 2025
Study Completion
August 5, 2025
Last Updated
August 27, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share