CClinicalTrials.gg
CompletedNCT06965907Updated Jul 29, 2025

Kinesiotaping on Hand Function in Computer Users

An interventional study of Kinesio Taping and Sham Taping in Computer-user Training, sponsored by Istinye University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-29.

Sponsored by Istinye University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

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.
02

Conditions studied

  • Computer-user Training

Keywords

  • kinesiotaping
  • sensation
  • dexterity
  • reaction time
  • athletic tape
03

In context

Lead sponsor

Istinye University is the lead sponsor of 207 studies on the registry; 88 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
34 participants (actual)

Study arms

  • Experimental
    Kinesio Taping group

    Other: Kinesio Taping

  • Sham comparator
    Sham Kinesio Taping group

    Other: Sham Taping

Interventions

  • OtherKinesio Taping

    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.

  • OtherSham Taping

    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.

06

What researchers measure

Primary outcomes

  1. Two-point Discrimination

    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.

    Time frame: Day 1

  2. Fine Motor Skills

    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: * Dominant Hand Task: The participant will insert as many pegs as possible into the holes using the dominant hand within 30 seconds. * Non-Dominant Hand Task: The same procedure will be repeated using the non-dominant hand. * Both Hands Task: Pegs will be inserted into the holes in pairs using both hands simultaneously over a 30-second period. * Assembly Task: Using both hands, the participant will assemble a sequence using pegs, washers, and collars for a duration of 60 seconds. The score will be determined by the number of pegs placed or sequences completed within the specified time limits.

    Time frame: Day 1

  3. Grip Strength

    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.

    Time frame: Day 1

  4. Reaction Time

    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

    Time frame: Day 1

07

Study locations

1 site
  • Istinye University Physiotherapy and Rehabilitation Application and Research Center (İSÜFİZYOTEM)
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06965907
Lead sponsor
Istinye University
Responsible party
Çiçek Günday (Asst. Prof., Istinye University) — Principal investigator
First posted
May 11, 2025
Start date
Mar 10, 2025
Primary completion
Jul 24, 2025
Completion
Jul 24, 2025
Last update
Jul 29, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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