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Instrument-assisted Soft Tissue Mobilization and Kinesiotape Application in Individuals With Chronic Neck Pain.

K

KTO Karatay University

Status

Completed

Conditions

Cervical Pain

Treatments

Other: Instrument Assisted Soft Tissue Mobilization
Other: Kinesiotape Application

Study type

Interventional

Funder types

Other

Identifiers

NCT04765670
KaratayUH2

Details and patient eligibility

About

Chronic neck pain causes errors in joint position sense. There are studies in the literature suggesting that instrument-assisted soft tissue mobilization and Kinesiotape applications improve the joint position sense. There is no study examining these applications acutely on joint position sense and pain in the cervical region. As a result of our study, we will compare the effects of single-session instrument-assisted soft tissue mobilization and Kinesiotape application on pain and joint position sense.

Full description

The study will be carried out on volunteers after the approval of the ethics committee. Before the research, individuals and / or their relatives will be informed about the purpose and content of the study. Volunteer individuals between the ages of 18-45 with chronic neck pain will be included in the study after obtaining their informed consent.

Participants will be randomly divided into two groups: Instrument assisted soft tissue mobilization and Kinesiotape Applications.

In the instrument-assisted soft tissue mobilization group, the trapezius and sternocleidomastoideus muscles will be applied in a single session for 90 seconds. Kinesiotape application will be applied to the trapezius and sternocleidomastoideus muscles in one session.

Pain will be evaluated with Visual Analog Scale and joint position sense will be evaluated with Cervical Range of Motion device before and after application.

Enrollment

40 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being diagnosed with chronic neck pain
  • Being in the age range of 18-45

Exclusion criteria

  • Those with acute injury or infection,
  • Those with open wounds,
  • Osteoporosis,
  • Hematoma,
  • Those with acute cardiac, liver and kidney problems,
  • Those with connective tissue disease, Rheumatoid arthritis, osteoarthritis, Cancer,
  • Those with circulation problems,
  • Those with peripheral vascular disease,
  • Epilepsy
  • Identified as a history of surgery in the cervical region

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups

Instrument Assisted Soft Tissue Mobilization
Experimental group
Description:
The instruments will be applied to the soft tissue at 30º-60º angles, with multi-directional "stroking" movements. Instrument Assisted Soft Tissue Mobilization will be applied to the trapezius and sternocleidomastoideus muscles of the participants for 90 seconds.
Treatment:
Other: Instrument Assisted Soft Tissue Mobilization
Kinesiotape Application
Experimental group
Description:
The application will be made from the insertion of the upper trapezoidal muscle to its origo . During taping, the patient will be allowed to sit in an upright position in a chair with a back, with the scapula fixed, without supporting the arms. Before taping, the patient will be positioned with the shoulder in adduction and the head in lateral flexion towards the contralateral side. The patient will be asked to perform shoulder abduction against resistance, and the insertion area of the upper trapezius fibers will be palpated. The initial 2-3 cm part of the band will be glued to the lateral of the acromion without stretching, after full (100%) stretching is applied to the 2-3 cm part of the band from the insertion area of the upper trapezoid fibers, the patient's head is rotated to the affected side and the arm part of the band is stretched along the muscle fibers. it will be glued up to the hairline without doing it.
Treatment:
Other: Kinesiotape Application

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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