Changes on Pain and Range of Motion by the Use of Kinesio Taping in Patients Diagnosed With Cervical Pain

Not Applicable

Completed

• Conditions: Mobility Limitation; Myofascial Trigger Point Pain
• Interventions: Device: Sham Kinesio Taping; Device: Kinesio Taping

• Registration Number: NCT02913976
• Lead Sponsor: Cardenal Herrera University

Brief Summary

The aim of this study is to demonstrate that the application of Kinesio Taping on a myofascial trigger point in the trapezius muscle able to cause a decrease of the pain and an increase of the cervical range of motion in patients diagnosed with cervical pain.

Detailed Description

The use of Kinesio Taping has become very popular for the treatment of many musculoskeletal disorders in recent decades. Of the six variants of application that has the Kinesio Taping, the space correction technique is suggested for pain management. The increased space achieved with this variant decreases the pressure by raising the skin directly over the treatment area, reducing chemical irritation receptors and therefore pain. The aim of this study is to demonstrate that the application of this variant of Kinesio Taping on a myofascial trigger point in the trapezius muscle able to cause a decrease of the pain and an increase of the cervical range of motion in patients diagnosed with cervical pain. For this, the pressure pain threshold will be measured with a algometer on the trigger point, the perception of pain with a visual analog scale and the range of motion with a cervical goniometer.

Study Timeline

• Status Verified: 2016-09
• Study First Submitted: 2016-09-18
• Study First Submitted QC: 2016-09-22
• Study First Posted: 2016-09-26
• Study Start: 2016-10
• Primary Completion: 2016-11
• Study Completion: 2016-12
• Last Update Submitted: 2016-12-21
• Last Update Posted: 2016-12-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Agree to participate in the study (signed informed consent)
• Presence of active myofascial trigger point in upper trapezius.
• Presence of neck pain

Exclusion Criteria

• Subjects in which not clearly identified myofascial trigger point in the upper trapezius .
• Subjects who suffer or have suffered pathologies of upper limb deformities or orthopedic injuries that can alter static and biomechanics of shoulder and neck.
• Subjects who suffer or have suffered rheumatic or neurological disease or chronic shoulder pain and/or neck
• Subjects diagnosed with fibromyalgia, myelopathy or radiculopathy.
• Subjects suffering from any psychiatric disorder (such as anxiety or depression).
• Subjects who have suffered post-traumatic alteration (whiplash type) or cervical surgery.
• Pregnancy risk of abortion.
• Have used analgesics in the 48 hours before participating in the study
• Subjects presenting any contraindications to the application of Kinesio Taping.
• Know the Kinesio Taping technique applied in the study.
• Be receiving physical therapy for any shoulder or neck pathology.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Sham Kinesio Taping	Sham Kinesio Taping	Four Kinesio Taping strips will be placed without tension on skin forming an asterisk. The point of intersection of the four strips will be just above the myofascial trigger point. The subject will remain three days with the strips on his skin
Kinesio Taping	Kinesio Taping	Four Kinesio Taping strips will be placed with tension on skin forming an asterisk. The point of intersection of the four strips will be just above the myofascial trigger point. The subject will remain three days with the strips on his skin

Primary Outcome Measures

Name	Time	Method
Changes in pressure pain threshold	At the beginning, immediately after intervention and at 72 hours	Is defined as the minimum force applied which induces pain on myofascial trigger point. Pressure will be applied with algometer

Secondary Outcome Measures

Name	Time	Method
Changes in pain perception	At the beginning, immediately after intervention and at 72 hours	It is an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage. Will be measured with a visual analog scale
Changes in cervical range of motion	At the beginning, immediately after intervention and at 72 hours	Cervical range of motion is measuring movement around this segment of the spine. Lateral flexion and rotation. Will be measured with a cervical goniometer

Trial Locations

Locations (1)

CEU Cardenal Herrera University; 🇪🇸 Moncada, Valencia, Spain