- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06965907
- Original Trial
Kinesiotaping on Hand Function in Computer Users
Immediate Effect of Kinesio Taping on Two-Point Discrimination, Fine Motor Skills, Grip Strength and Reaction Time on Computer Users
This study aims to investigate whether kinesio taping contributes to improved hand function in individuals who frequently use computers. The effectiveness of kinesio taping will be compared to sham taping in order to determine its impact. Participants will be randomly assigned to one of two groups: a kinesio taping group or a sham taping group. Taping will be applied to the forearm. Functional assessments will be conducted at three time points: prior to taping, immediately after taping, and 30 minutes post-taping. The following evaluations will be performed:
- Two-point discrimination test to assess touch sensitivity
- Purdue Pegboard test to evaluate fine motor skills
- Grip strength test using a hand dynamometer
- Visual reaction time test utilizing a light-based device All procedures will be completed in a single study session.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey
- Istinye University Physiotherapy and Rehabilitation Application and Research Center (ISUFIZYOTEM)
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants must use a computer ≥ 2 hours per day.
- Participants must be between the ages of 18 and 50.
- If the participants are employed, they must not have changed professions in the last 6 months.
- If the participants are students, their student status must have been ongoing for at least 6 months.
Exclusion Criteria:
- A diagnosed history of neuropathy or common diseases associated with peripheral neuropathy.
- Diagnosed musculoskeletal disorders related to the neck and upper extremities.
- Presence of symptoms suggestive of nerve entrapment.
- Having a condition that prevents the application of physical tests (e.g., limited range of joint motion, deformities, fractures, arthritis, etc.).
- Allergic reaction to kinesiology tape.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kinesio Taping group
|
The participant will be seated upright in a chair with the elbow flexed at 90 degrees.
The forearm under examination will be placed in a pronated position, and the wrist will be maintained in a neutral position.
I-shaped kinesio taping will be applied as described by Mohammadi et al.
Prior to taping, the extensor surface will be cleaned using a cotton swab moistened with alcohol.
The tape length will be measured from a point 2 cm distal to the lateral epicondyle to the radial styloid process.
Each end of the tape will be 2 cm in length (totaling 4 cm for both ends).
To achieve 35% tension, the following formula will be used: (L - 4) / 1.35 + 4. In this formula, L represents the total length of the tape, 4 is the combined length of the two tape ends, and 1.35 corresponds to the factor required to achieve the desired 35% tension.
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Sham Comparator: Sham Kinesio Taping group
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The participant will be seated in a chair with the forearm resting comfortably.
The tape will be applied to the middle of the forearm without any tension.
The taping will be performed from the medial to the lateral direction.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Two-point Discrimination
Time Frame: Day 1
|
This test measures an individual's ability to perceive two closely spaced points touching the skin simultaneously, reflecting tactile spatial acuity.
During the evaluation, the contact points will initially be set 14 mm apart, with the distance reduced by 1 mm at each step.
Adjustments will continue until the participant can no longer distinguish two separate points.
The final distance at which two points are still perceived as distinct will be recorded.
|
Day 1
|
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Fine Motor Skills
Time Frame: Day 1
|
Purdue Pegboard Test will be used. The participant will be seated at a table with the pegboard placed directly in front of them. The test consists of four tasks:
The score will be determined by the number of pegs placed or sequences completed within the specified time limits. |
Day 1
|
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Grip Strength
Time Frame: Day 1
|
Maximum grip strength will be measured using a JAMAR Hydraulic Hand Dynamometer.
The participant will be seated upright with the elbow flexed at 90 degrees, and the forearm and wrist maintained in a neutral position.
Participants will be instructed to squeeze the dynamometer with maximum effort for five seconds.
Three trials will be conducted, with a 30-second rest period between each attempt.
The highest value obtained will be recorded as the maximum grip strength.
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Day 1
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Reaction Time
Time Frame: Day 1
|
Reaction time will be recorded using the BlazePod Trainer device.
BlazePod is a wireless lighting system consisting of LED pods and a control unit.
Participants will begin the test in a seated position, placing their hands on the table with palms facing downward and spaced 40 cm apart.
The BlazePod will be positioned at the center of the table, 20 cm away from each hand, and will emit random light signals.
Participants will be instructed to tap the illuminated pod as quickly as possible upon activation.
The test will last for 15 seconds, and the average reaction time of all hits during the activity will be recorded
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Day 1
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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
Other Study ID Numbers
- 29032002
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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