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

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.

Study Overview

• Status: Recruiting
• Conditions: Neck Pain
• Intervention / Treatment: Other: Kinesiology taping; Other: Self-mobilization

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.

• Study Type: Interventional
• Enrollment (Anticipated): 32
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Associate Professor; Phone Number: +905554178535; Email: rustem.mustafaoglu@iuc.edu.tr
• Study Contact Backup: Name: Seth K Agyenkwa; Phone Number: +905343007484; Email: sethkwameagyenkwa@ogr.iuc.edu.tr

Study Locations

• Turkey
  • Istanbul, Turkey
    • Recruiting
    • İstanbul University-Cerrahpaşa
    • Contact: Seth K Agyenkwa; Phone Number: +905343007484; Email: sethkwameagyenkwa@ogr.iuc.edu.tr
    • Contact: Rustem Mustafaoglu; Phone Number: +905554178535; Email: rustem.mustafaoglu@iuc.edu.tr
  • Istanbul, Turkey
    • Recruiting
    • Istanbul University, Cerrahpaşa
    • Contact: Seth K Agyenkwa; Phone Number: +905343007484; Email: sethkwameagyenkwa@ogr.iuc.edu.tr
    • Contact: Rustem Mustafaoglu; Phone Number: +905554178535; Email: rustem.mustafaoglu@iuc.edu.tr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

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).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: SINGLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
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; 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.
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; 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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.	Baseline, before treatment
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.	One week post-treatment (week 5)
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.	One-month follow up (week 9)
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.	Baseline, before treatment
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.	One week post-treatment (week 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.	One-month follow up (week 9)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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.	Baseline, before treatment
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.	One week post-treatment (week 5)
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.	One-month follow up (week 9)

Collaborators and Investigators

• Sponsor: Istanbul University - Cerrahpasa (IUC)

Study record dates

Study Major Dates

• Study Start (ACTUAL): November 16, 2022
• Primary Completion (ANTICIPATED): May 1, 2023
• Study Completion (ANTICIPATED): June 1, 2023

Study Registration Dates

• First Submitted: January 17, 2023
• First Submitted That Met QC Criteria: January 29, 2023
• First Posted (ACTUAL): February 8, 2023

Study Record Updates

• Last Update Posted (ACTUAL): February 8, 2023
• Last Update Submitted That Met QC Criteria: January 29, 2023
• Last Verified: January 1, 2023

More Information

Terms related to this study

• Keywords: neck pain; neck disability; kinesio-taping; self-mobilization; electronic device users
• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Neck Pain
• Other Study ID Numbers: E-74555795-050.01.04-533346

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No