- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06608615
the Instant Effect of Rigid and Kinesio Taping Techniques in Stroke Individuals With Foot Drop
Investigation of the Instant Effect of Rigid and Kinesio Taping Techniques on Physical Performance, Gait and Physiological Expenditure Index in Stroke Individuals With Foot Drop
Stroke individuals with foot drop experience poor physical performance and walking problems. Physiological energy consumption also increases due to balance and walking problems. The aim of this study is to investigate the immediate effects of rigid and kinesio taping techniques on physical performance, gait and physiological expenditure index in stroke individuals with foot drop, and also to examine whether these approaches are superior to each other.
As a result of this study, it was seen that Rigid Taping and Kinesio Taping were effective in stroke individuals with foot drop. When we compared the groups, it was determined that both taping methods produced similar effects.
Study Overview
Status
Intervention / Treatment
Detailed Description
Stroke individuals with foot drop experience poor physical performance and walking problems. Physiological energy consumption also increases due to balance and walking problems. The aim of this study is to investigate the immediate effects of rigid and kinesio taping techniques on physical performance, gait and physiological expenditure index in stroke individuals with foot drop, and also to examine whether these approaches are superior to each other.
40 individuals diagnosed with hemorrhagic or ischemic stroke were included in the study. Individuals were divided into two groups: Rigid Taping Group (n=20) and Kinesio Taping Group (n=20). The physical performances of the individuals participating in the study were evaluated with the One-Leg Standing Test, Timed Up and Go Test (TUG) and the Sit-Up-from-Chair Test (SUCT), their walking speed was evaluated with the 10 Meter Walk Test, and the spatiotemporal characteristics of the gait were evaluated with gait analysis on powdered ground. Physiological Expenditure Index (FHI) was calculated with 6 Minute Walk Test (6MWT) results. Evaluations were recorded by the same physiotherapist before and after taping.
As a result of this study, it was seen that Rigid Taping and Kinesio Taping were effective in stroke individuals with foot drop. When we compared the groups, it was determined that both taping methods produced similar effects. We believe that adding rigid or kinesio taping applications for foot drop to the rehabilitation program of stroke individuals with drop foot will increase the success of the treatment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Kırıkkale, Turkey
- Kırıkkale University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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 |
|---|---|
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Experimental: Kinesio Taping Group
Persons who will undergo kinesio taping
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Facilitation (Functional) Technique for Tibialis Anterior Muscle: The patient sits with his leg extended. The ankle is placed in eversion and dorsi flexion. After one end of the I tape is adhered to the upper part of the Tibia, the other end is adhered to the dorsal surface of the foot with almost 100% tension. During the application, origin and insertion points are considered as the beginning and end. Then, plantar fexion is performed on the ankle and the remaining non-stick part is glued. Functional Correction Technique: Correction technique is used to ensure full contact of the foot with the ground. The subtalar joint is positioned in eversion and taping is applied starting from under the medial malleolus, without tension until the lateral outer edge of the calceneus, and then with 100% tension, continuing until 10-15 cm below the head of the fibula. No tension is applied in the last 5 cm
Other Names:
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Experimental: Rigid Taping group
Persons to whom rigid taping will be performed
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Talus Stabilization Taping: The affected ankle of the person to be taped was placed on a chair and asked to bring this foot to a neutral position by advancing the tibia over the foot through knee flexion while standing. Starting from the talus of the ankle, maximum tension was applied towards the medial and lateral malleolus. Inversion Lock: This lock looks like an inverted 6 when viewed from the front and is used to restrict inversion movement. After the underwrap and anchor were applied, the tape was applied starting from the outer malleolus level. It was glued on itself by proceeding diagonally in front of the foot, passing it in front of the inner malleolus, passing under the foot and in front of the outer malleolus and closing the subtalar area, and the taping was completed by making an anchor on the upper side.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Timed up and go test
Time Frame: 3 minutes
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"The timed up and go measures, in seconds, the time taken by an individual to stand up from a standard arm chair (approximate seat height of 46 cm), walk a distance of 3 metres, turn, walk back to the chair and sit down again.
The subject wears his regular footwear and uses his customary walking aid (none, cane, or walker).
No physical assistance is given.
He starts with his back against the chair, his arms resting on the chair's arms and his walking aid at hand.
He is instructed that, on the word "go", he is to get up and walk at a comfortable and safe pace to a line on the floor 3 metres away, turn, return to the chair and sit down again.
The subject walks through the test once before being timed in order to become familiar with the test.both
taping methods produced similar effects.
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3 minutes
|
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10 metre walking test
Time Frame: 1 minutes
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Gait speed was based on the average of two trials of the 10-m TWT in order to reduce measurement error.
Patients were instructed to walk independently from other people as fast and safely as possible, and were allowed to use a walking aid if needed.
The 10 metres had to be free of obstacles and turns.
program of stroke individuals with drop foot will increase the success of the treatment.
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1 minutes
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Sit up and chair test
Time Frame: 1 minutes
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ubjects began the test sitting on a 47 cm-high chair, positioned with the feet hip width apart, toes under knees and arms folded across their chest.
The investigators recorded the length of time to the nearest tenth of a second it took for subjects to rise and sit back down five consecutive times without the use of their arms.
Participants were given one practice trial to familiarize themselves with the procedure.kullanımında
etkili olduğunu göstermektedir.
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1 minutes
|
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six minute walk test
Time Frame: 10 minutes
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The functional capacity of the individuals was evaluated with 6MWT.
The measurements were made in line with the recommendations of the American Thoracic Society.
The individuals were asked to walk in a 30-m corridor at their own walking speed for 6 min as far as possible.
The individuals were allowed to stop and rest during the test, which was repeated twice every other day.
The maximum 6 min walking dis- tance was recorded in meters.
|
10 minutes
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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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KırıkkaleüniylÖmerKaya
- Ömer Kaya (Other Identifier: Kırıkkale Üniversitesi)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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