- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07138118
- Original Trial
Study of Blood Flow Restriction and Cognitive-Motor Dual Task Training to Improve Strength, Gait, and Balance in People With Subacute Stroke
Effects of an Individualized Blood Flow Restriction Training Combined With a Cognitive-Motor Dual Task Intervention on Lower Limb Strength, Gait Ability, and Fall Stability in Subacute Stroke Patients: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Subacute stroke is defined as the period between 7 days and 6 months after stroke onset, a critical window during which neuroplasticity and functional recovery are highly active. During this phase, individualized and task-specific interventions can enhance motor recovery. Blood flow restriction (BFR) training is a promising low-load exercise modality that induces physiological effects similar to high-intensity training by restricting venous return using a proximal cuff. Studies suggest that BFR training at 40% of arterial occlusion pressure (AOP) can safely stimulate muscle hypertrophy and strength, particularly in populations with limited exercise capacity, such as stroke survivors.
Additionally, dual task training, which combines motor and cognitive tasks, has been shown to improve executive function and gait performance by increasing prefrontal cortex activity. While each approach has independent benefits, the combination of peripheral muscle activation through BFR and central stimulation via cognitive-motor dual tasks may provide synergistic effects on functional recovery.
This randomized controlled trial will compare an intervention group receiving BFR training (40% AOP) with concurrent dual task gait training to a control group performing the same cognitive-motor dual tasks without BFR. Both groups will train three times per week for 5 weeks. Outcome measures will assess changes in lower limb strength, gait ability, and fall stability before and after the intervention. The study also addresses safety and standardization concerns in BFR application by using pulse oximeter-based AOP measurement protocols.
By providing evidence on the efficacy and safety of combining BFR and dual-task training in subacute stroke rehabilitation, this study aims to contribute to the development of individualized, clinically applicable intervention strategies.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Seoul
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Seoul, Seoul, South Korea, 01795
- Sahmyook University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients diagnosed with subacute stroke within 1 to 6 months after onset
- Able to walk at least 10 meters, with or without assistive devices
- Modified Ashworth Scale score less than 1
- Korean Mini-Mental State Examination (K-MMSE) score of 24 or higher
Exclusion Criteria:
- History of psychiatric disorders or cognitive impairment
- Presence of peripheral neuropathy
- Resting systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg despite medication
- Diagnosis of heart failure or unstable angina
- History of bypass surgery within the past 3 months
- Serious musculoskeletal disorders affecting gait (e.g., amputation, fracture)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental: BFR + Dual Task
Participants in this group will perform cognitive-motor dual task training while wearing blood flow restriction (BFR) cuffs set at 40% of their individualized arterial occlusion pressure (AOP).
The training consists of three sessions per week for five weeks.
Each session lasts 40 minutes and includes tasks such as forward walking, obstacle crossing, and seated-to-stand with concurrent verbal fluency or serial subtraction tasks.
|
Participants will undergo lower limb resistance and gait training while wearing blood flow restriction cuffs at 40% of their individualized arterial occlusion pressure.
Tasks include walking, sit-to-stand, and obstacle crossing combined with verbal fluency or serial subtraction.
Training is performed 3 times per week for 5 weeks.
Other Names:
|
|
Active Comparator: Active Comparator: Dual Task Only
Participants in this group will perform the same cognitive-motor dual task training as the experimental group but without blood flow restriction.
The training will also be conducted three times per week for five weeks, with each session lasting 40 minutes.
Tasks include walking and obstacle navigation combined with verbal fluency or serial subtraction exercises.
|
Participants will perform the same cognitive-motor dual task training without blood flow restriction.
Tasks include forward walking, obstacle crossing, and sit-to-stand exercises with concurrent cognitive tasks such as verbal fluency or serial subtraction.
Training is performed 3 times per week for 5 weeks.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
5 Times Sit-to-Stand Test (5STS)
Time Frame: Baseline and after 5 weeks of intervention
|
Lower limb strength will be assessed using the Five Times Sit-to-Stand Test.
A shorter time indicates better performance.
|
Baseline and after 5 weeks of intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
10-Meter Walk Test (10MWT)
Time Frame: Baseline and after 5 weeks of intervention
|
Walking speed (m/s) will be measured over a middle 10-meter segment of a 14-meter walking path.
Higher values indicate better performance.
|
Baseline and after 5 weeks of intervention
|
|
Timed Up and Go Test (TUG)
Time Frame: Baseline and after 5 weeks of intervention
|
Shorter completion time on the TUG indicates improved functional balance and mobility.
|
Baseline and after 5 weeks of intervention
|
|
Korean Version of Falls Efficacy Scale - International (KFES-I)
Time Frame: Baseline and after 5 weeks of intervention
|
KFES-I assesses confidence in avoiding falls during daily activities.
Lower scores indicate higher confidence.
|
Baseline and after 5 weeks of intervention
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Functional Gait Assessment (FGA)
Time Frame: Baseline and after 5 weeks of intervention
|
The FGA is a 10-item test that assesses postural stability during various walking tasks.
Higher scores indicate better functional gait and balance.
|
Baseline and after 5 weeks of intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Seungwon Lee, PhD, Sahmyook University
Publications and helpful links
General Publications
- Liu YC, Yang YR, Tsai YA, Wang RY. Cognitive and motor dual task gait training improve dual task gait performance after stroke - A randomized controlled pilot trial. Sci Rep. 2017 Jun 22;7(1):4070. doi: 10.1038/s41598-017-04165-y.
- Ahmed I, Mustafaoglu R, Erhan B. The effects of low-intensity resistance training with blood flow restriction versus traditional resistance exercise on lower extremity muscle strength and motor functionin ischemic stroke survivors: a randomized controlled trial. Top Stroke Rehabil. 2024 May;31(4):418-429. doi: 10.1080/10749357.2023.2259170. Epub 2023 Sep 19.
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
- SYU 2025-06-027-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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