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Self-Mobilization Versus Kinesio-Taping on the Cervical Region in Electronic Device Users

Effectiveness of Self-Mobilization Versus Kinesio-Taping on the Cervical Region in Electronic Device Users

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05717868
Enrollment
32
Registered
2023-02-08
Start date
2022-11-16
Completion date
2023-06-30
Last updated
2023-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

kinesio-taping, self-mobilization, neck disability, neck pain, electronic device users

Brief summary

The purpose of this clinical trial is to compare the effectiveness of kinesio-taping versus self-mobilization applied to the cervical region of long-duration electronic device users.

Detailed description

There is increasing use of electronic devices among individuals due to technological advancement and increasing work demands. The prolong use of these devices may result to discomfort in the neck and impairments in cervical range of motion, proprioceptive sense, muscle activities, and disability among users of electronic devices. Kinesio-taping and self-mobilization in the cervical region may improve function, and reduce disability. Therefore the aim of this study is to compare the effectiveness of kinesio-taping against self-mobilization among long-duration electronic device users. Participants will be randomized into either a kinesio-taping or self-mobilization group. Treatment will be administered within a four-week period. Participants will be evaluated at baseline, post-intervention and at one-month follow-up.

Interventions

OTHERKinesiology taping

5 cm wide and 0.5 mm thick waterproof, porous and adhesive tape will be applied to the posterior neck of the participants while sitting comfortably in a neutral position. The first tape (Y-strip) is placed over the posterior cervical extensor muscles with approximately 25% tension. The top strip will be placed perpendicular to the Y strip on the mid-cervical region. The participant's cervical spine is flexed to obtain tension in the posterior structures.

The towel will be placed on the posterior arch of the fifth cervical vertebra and pulled horizontally across the face. The participant will be instructed to apply pressure to the towel and turn their head to the restricted side, then maintain the finishing interval for three seconds. The participant will be asked to apply extreme pressure in the bending position with towel support. The procedure should be painless and repeated 10 times.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Complain of pain in the neck * Using electronic devices (including smart phones, desktop computers, laptops, tablets) for at least 4 hours a day, * Using electronic devices for at least 6 months, * Volunteering to participate in the study

Exclusion criteria

* Having a history of allergic reaction, * Having previous cervical pathologies such as cervical spondylolisthesis, disc herniation, rheumatoid arthritis, muscle or ligament injury or strain, * Having had neck or shoulder surgery, * Having a neurological deficit (eg numbness, muscle weakness and loss of sensation).

Design outcomes

Primary

MeasureTime frameDescription
Upper trapezius electrical muscle activityBaseline, before treatmentThe Trigno Avanti SEMG system (Delsys inc., Boston) will be used to measure the surface electromyographic activities of the upper trapezius muscle.The electrodes will be placed over the right and left trapezius muscle along the lines connecting the spinous process of the seventh cervical vertebra (C7) to the right and left acromion.
Visaul Analogue Scale (VAS)Baseline, before treatmentParticipants will indicate their pain level on a 10 cm horizontal line; where 0 indicates no pain and 1- the worst possible pain the subject could experience.

Secondary

MeasureTime frameDescription
Joint Position Sense ErrorBaseline, before treatmentJoint position sense error of the cervical joint will be tested in flexion, extension, left and right rotation using a laser pointer.

Countries

Turkey (Türkiye)

Contacts

Primary ContactAssociate Professor
rustem.mustafaoglu@iuc.edu.tr+905554178535
Backup ContactSeth K Agyenkwa
sethkwameagyenkwa@ogr.iuc.edu.tr+905343007484

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026