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

I

Istanbul University - Cerrahpasa (IUC)

Status

Enrolling

Conditions

Neck Pain

Treatments

Other: Self-mobilization
Other: Kinesiology taping

Study type

Interventional

Funder types

Other

Identifiers

NCT05717868
E-74555795-050.01.04-533346

Details and patient eligibility

About

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.

Full 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.

Enrollment

32 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Kinesio-taping group
Experimental group
Description:
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.
Treatment:
Other: Kinesiology taping
Self-mobilization group
Experimental group
Description:
Self-SNAG technique will be applied by the participants with the help of a towel, and performed for a four week period.
Treatment:
Other: Self-mobilization

Trial contacts and locations

2

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Central trial contact

Seth K Agyenkwa; Associate Professor

Data sourced from clinicaltrials.gov

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