CClinicalTrials.gg
Status unknownNCT05717868Updated Feb 8, 2023

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

An interventional study of Kinesiology taping and Self-mobilization in Neck Pain, sponsored by Istanbul University - Cerrahpasa. Status unknown at 2 sites in Turkey. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-02-08.

Sponsored by Istanbul University - Cerrahpasa · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2023), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Neck Pain

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Keywords

  • kinesio-taping
  • self-mobilization
  • neck disability
  • neck pain
  • electronic device users
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's planned enrollment of 32 is below the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 680 studies on the registry; 207 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts 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

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).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
32 participants (estimated)

Study arms

  • Experimental
    Kinesio-taping group

    Kinesio-tape will be applied from the dorsal region (T1-T2) to the upper cervical region (C1-C2), two times weekly in a period of four weeks.

    Other: Kinesiology taping

  • Experimental
    Self-mobilization group

    Self-SNAG technique will be applied by the participants with the help of a towel, and performed for a four week period.

    Other: Self-mobilization

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.

  • OtherSelf-mobilization

    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.

06

What researchers measure

Primary outcomes

  1. Upper trapezius electrical muscle activity

    The 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.

    Time frame: Baseline, before treatment

  2. Upper trapezius electrical muscle activity

    The 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.

    Time frame: One week post-treatment (week 5)

  3. Upper trapezius electrical muscle activity

    The 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.

    Time frame: One-month follow up (week 9)

  4. Visaul Analogue Scale (VAS)

    Participants 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.

    Time frame: Baseline, before treatment

  5. Visaul Analogue Scale (VAS)

    Participants 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.

    Time frame: One week post-treatment (week 5)

  6. Visaul Analogue Scale (VAS)

    Participants 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.

    Time frame: One-month follow up (week 9)

Secondary outcomes

  1. Joint Position Sense Error

    Joint position sense error of the cervical joint will be tested in flexion, extension, left and right rotation using a laser pointer.

    Time frame: Baseline, before treatment

  2. Joint Position Sense Error

    Joint position sense error of the cervical joint will be tested in flexion, extension, left and right rotation using a laser pointer.

    Time frame: One week post-treatment (week 5)

  3. Joint Position Sense Error

    Joint position sense error of the cervical joint will be tested in flexion, extension, left and right rotation using a laser pointer.

    Time frame: One-month follow up (week 9)

07

Study locations

2 of 2 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 8, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05717868
Lead sponsor
Istanbul University - Cerrahpasa
Responsible party
Seth Kwame Agyenkwa (Researcher, Istanbul University - Cerrahpasa) — Principal investigator
First posted
Feb 8, 2023
Start date
Nov 16, 2022
Primary completion
May 2023 (estimated)
Completion
Jun 2023 (estimated)
Last update
Feb 8, 2023

Study contacts

Associate Professor
Contact
rustem.mustafaoglu@iuc.edu.tr
+905554178535
Seth K Agyenkwa
Contact
sethkwameagyenkwa@ogr.iuc.edu.tr
+905343007484
Rustem Mustafaoglu
principal investigator · Istanbul University - Cerrahpasa

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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