- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06938477
Thera-Trainer Exercise Effects on Motor and Cognitive Outcomes in Stroke: RCT
EFFECTS OF THERA-TRAINER BASED EXERCISES ON MOTOR AND COGNITIVE PERFORMANCE AMONG HEMİPARATİC STROKE PATIENTS. A RANDOMİSED CONTROL TRİAL
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Stroke is a leading cause of death and disability worldwide. It can be generally classified as ischemic stroke and hemorrhagic stroke. Ischemic stroke is defined as an infarction of the brain, spinal cord, or retina and accounts for approximately 70% of all strokes. Hemorrhagic stroke occurs as a result of intracerebral hemorrhage and subarachnoid hemorrhage (Campbell et al., 2019).Technology-assisted rehabilitation supports recovery by providing high-intensity, repetitive, and task-specific treatment, facilitating the restoration of upper limb function. Studies on technology-based rehabilitation for upper extremity recovery utilize various devices. The THERA-Trainer Tigo, for instance, is designed to mobilize individuals with restricted movement abilities caused by trauma or other conditions. It is suitable for both passive and active motion training. Therapy with active-passive exercise devices promotes rehabilitation through natural and rhythmic movements. It accommodates a wide range of patients-from wheelchair users to those capable of walking-by enabling nearly all individuals in the rehabilitation process to actively participate in cycling exercises .
However, there is a limited body of research exploring the relationship between cognitive and motor performance functions during THERA-Trainer-based exercises. This study aims to address this gap by providing clinicians with insights into progression during evaluation and treatment phases, enhancing therapeutic strategies, and contributing to the academic knowledge base for researchers.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Mersi̇n
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Tarsus, Mersi̇n, Turkey, 33400
- Fatma kübra çekok
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having had an ischemic or hemorrhagic stroke for the first time
- Those with a Montreal Cognitive Assessment (MOCA) score above 21,
- Individuals with a functional level below 4 according to the modified Rankin scale (MRS),
- Individuals with upper extremity spasm below 3 according to the modified Ashword scale (MAS)
Exclusion Criteria:
- Montreal Cognitive Assessment (MOCA) score of less than 21,
- Upper extremity spasticy of over 3 according to MAS,
- Patients with subluxation and fracture risk in the shoulder,
- Agnosia or visual impairment,
- Limited joint movement in the hemiplegic side upper extremity,
- Patients who have undergone any botulinum toxin application or surgery in the last 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: THERA-TRAINER BASED EXERCISES
Participants in the exercise arm will engage in structured, Thera-Trainer-based exercise programs tailored to their motor and cognitive rehabilitation needs.
The intervention focuses on combining motor and cognitive tasks to maximize recovery outcomes.
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The interventions will carried out two days a week and 40 minutes for eight weeks
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Experimental: Functional Stroke Training
To enhance motor recovery, functional independence, and cognitive performance in stroke patients
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he interventions will carried out two days a week and 40 minutes for eight weeks
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mini Mental Test
Time Frame: Eight weeks
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The Mini Mental State Examination (MMSE) is a widely used tool for assessing cognitive function, particularly in screening for dementia and monitoring cognitive changes over time.
It evaluates different cognitive domains, including orientation, registration, attention, calculation, recall, language, and visual-spatial skills.
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Eight weeks
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Digit Span Test
Time Frame: Eight weeks
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The Digit Span Test is a cognitive assessment tool used to evaluate working memory, attention, and concentration.
It is often part of broader neuropsychological evaluations and can assess both forward and backward digit span.
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Eight weeks
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Frenchay Arm Test
Time Frame: Eight weeks
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The Frenchay Arm Test involves 5 tasks, each graded as pass (1 point) or fail (0 points) based on the patient's ability to complete the task.
The tasks progress in difficulty and assess various aspects of upper limb function.
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Eight weeks
|
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Time Up Go Test (TUG)
Time Frame: Eight weeks
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The Timed Up and Go Test (TUG) is a simple and widely used assessment tool to evaluate mobility, balance, and functional independence.
It is particularly useful for identifying fall risk in older adults and individuals with neurological or musculoskeletal impairments.
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Eight weeks
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Fugl Meyer Assesment
Time Frame: Eight weeks
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The test examines reflex activity, voluntary movements within, partially out and independent of synergies (22).
The scale includes 33 items divided into 4 subscales: shoulder/elbow (A, 18 items), wrist (B, 5 items), hand (C, 7 items) and coordination/ speed (D, 3 items).
Each item is scored on an ordinal 3-point scale, where 2 points are assigned when the movement is performed fully, 1 point when performed partially, and 0 points when the movement cannot be performed.
A total score of 66 indicates better sensorimotor function
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Eight weeks
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Five Time Sit to Stand
Time Frame: Eight weeks
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The Five Times Sit-to-Stand Test (FTSST) is a simple, reliable, and functional test used to assess lower limb strength, balance, and mobility.
It is widely applied in clinical and research settings for evaluating physical performance in various populations, including older adults and individuals with neuromuscular conditions.The individual sits in a standard chair (seat height ~43-45 cm) without armrests.The chair is placed against a wall or a stable surface to prevent movement.The participant starts seated with their back against the chair and feet flat on the floor, arms crossed over the chest.On the signal "Go," they are instructed to stand up fully and sit back down as quickly as possible, repeating this motion five times.The test begins at the word "Go" and ends when the participant fully stands after the fifth repetition.A stopwatch is used to record the total time taken.
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Eight weeks
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2 (Other Identifier: Instituto Cardiovascular de Buenos Aires)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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