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Effects of Kinesio Taping vs Jones Technique on Myofascial Trigger Points in Cervicalgia.

Primary Purpose

Cervicalgia

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Jones technique
Kinesiotape
Sponsored by
Blanca González Sanchez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervicalgia focused on measuring Cervicalgia, cinta de kinesio, Técnica de Jones, fisioterapia, puntos de activación.

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of latent PGM in the upper trapezius Have been working for more than 6 months in the center or company Work more than 4 hours a day with the computer Be over 18 years of age and under 64 years of age Exclusion Criteria: Diagnosis of fibromyalgia Having suffered a cervical sprain Diagnosis of radiculopathy, cervical spine surgery Medical contraindications to neuromuscular bandaging or Jones technique Diseases such as diabetes and cancer, pregnancy, and any other pathology that produces neck pain other than that specified in the objective of the study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Experimental

    Arm Label

    Jones technique group

    kinesio tapping group

    combined therapy group

    Arm Description

    Performs Jones technique 12 participants.

    Performs kinesiotape 14 participants.

    Performs Jones technique and kinesiotape 12 participants.

    Outcomes

    Primary Outcome Measures

    Change from Baseline VAS at 4 weeks of treatment and at the 2-week follow-up
    Visual Analogue Scale (VAS), consisting of a 10 cm line representing the continuous spectrum of painful experience. Only at the ends appear descriptions, "no pain" at one end and "worst pain imaginable" at the other, with no other description along the line. The subject will subjectively estimate his or her level of pain by indicating it on the ruler
    Change from Baseline UDP at 4 weeks of treatment and at the 2-week follow-up
    Measurement of the pressure pain threshold (UDP) This is performed using a pressure algometer that aims to objectify the ability of muscle fibers to adapt to compression on underlying planes
    Change from Baseline NDI at 4 weeks of treatment and at the 2-week follow-up
    Neck Disability Index (NDI), a questionnaire for self-assessment of function and activity disability in patients with neck pain. It consists of 10 items referring to functional activities, pain intensity, concentration and headache. The maximum score is 50 points, so that the higher the score the worse the function
    Change from Baseline GONIOMETER at 4 weeks of treatment and at the 2-week follow-up
    Goniometer, instrument used for the study of joint mobility (MA). Cervical flexion, right and left lateralizations, and right and left rotations were evaluated. Each measurement was made three times with a separation of 30 seconds in time, taking the average between the three measurements.

    Secondary Outcome Measures

    Full Information

    First Posted
    June 10, 2023
    Last Updated
    June 30, 2023
    Sponsor
    Blanca González Sanchez
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05939557
    Brief Title
    Effects of Kinesio Taping vs Jones Technique on Myofascial Trigger Points in Cervicalgia.
    Official Title
    Effects of Kinesio Taping vs Jones Technique on Myofascial Trigger Points in Cervicalgia: a Pilot Study of a Randomised Control Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    March 1, 2015 (Actual)
    Primary Completion Date
    April 1, 2015 (Actual)
    Study Completion Date
    June 30, 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Blanca González Sanchez

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    A large number of workers in different sectors suffer from musculoskeletal neck disorders, which are the most common work-related illness in Europe. A multitude of combinations of techniques can be used to treat these conditions, including recorded film and the Jones technique. This pilot study examines the efficacy of Kinesio taping and the Jones technique in improving pain, joint range of motion and muscle tension in active subjects with latent myofascial trigger points. A clinical trial was conducted with 38 patients with neck pain. The sample was randomly distributed into three groups: a Jones technique group, a kinesio taping group and a combined therapy group in which both techniques were performed. The duration of treatment was 4 weeks, with a follow-up of 2 weeks. Cervical spine joint range of motion, pain and functional disability were assessed with the goniometer, the visual analogue scale, the pressure algometer and the cervical disability index.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cervicalgia
    Keywords
    Cervicalgia, cinta de kinesio, Técnica de Jones, fisioterapia, puntos de activación.

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    38 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Jones technique group
    Arm Type
    Experimental
    Arm Description
    Performs Jones technique 12 participants.
    Arm Title
    kinesio tapping group
    Arm Type
    Experimental
    Arm Description
    Performs kinesiotape 14 participants.
    Arm Title
    combined therapy group
    Arm Type
    Experimental
    Arm Description
    Performs Jones technique and kinesiotape 12 participants.
    Intervention Type
    Procedure
    Intervention Name(s)
    Jones technique
    Intervention Description
    is a gentle soft tissue manipulation consisting of a passive procedure that positions the body in a position of comfort to release tissue that compresses or shortens the body structure (muscle contraction and joint dysfunction)
    Intervention Type
    Device
    Intervention Name(s)
    Kinesiotape
    Intervention Description
    KT has an S-shaped glue, which lifts the skin, thus improving blood and lymphatic circulation, with the intention of relieving pain and improving musculoskeletal diseases especially in sports
    Primary Outcome Measure Information:
    Title
    Change from Baseline VAS at 4 weeks of treatment and at the 2-week follow-up
    Description
    Visual Analogue Scale (VAS), consisting of a 10 cm line representing the continuous spectrum of painful experience. Only at the ends appear descriptions, "no pain" at one end and "worst pain imaginable" at the other, with no other description along the line. The subject will subjectively estimate his or her level of pain by indicating it on the ruler
    Time Frame
    time 0, after 4 weeks of treatment, and at the 2-week follow-up
    Title
    Change from Baseline UDP at 4 weeks of treatment and at the 2-week follow-up
    Description
    Measurement of the pressure pain threshold (UDP) This is performed using a pressure algometer that aims to objectify the ability of muscle fibers to adapt to compression on underlying planes
    Time Frame
    time 0, after 4 weeks of treatment, and at the 2-week follow-up
    Title
    Change from Baseline NDI at 4 weeks of treatment and at the 2-week follow-up
    Description
    Neck Disability Index (NDI), a questionnaire for self-assessment of function and activity disability in patients with neck pain. It consists of 10 items referring to functional activities, pain intensity, concentration and headache. The maximum score is 50 points, so that the higher the score the worse the function
    Time Frame
    time 0, after 4 weeks of treatment, and at the 2-week follow-up
    Title
    Change from Baseline GONIOMETER at 4 weeks of treatment and at the 2-week follow-up
    Description
    Goniometer, instrument used for the study of joint mobility (MA). Cervical flexion, right and left lateralizations, and right and left rotations were evaluated. Each measurement was made three times with a separation of 30 seconds in time, taking the average between the three measurements.
    Time Frame
    time 0, after 4 weeks of treatment, and at the 2-week follow-up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    64 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of latent PGM in the upper trapezius Have been working for more than 6 months in the center or company Work more than 4 hours a day with the computer Be over 18 years of age and under 64 years of age Exclusion Criteria: Diagnosis of fibromyalgia Having suffered a cervical sprain Diagnosis of radiculopathy, cervical spine surgery Medical contraindications to neuromuscular bandaging or Jones technique Diseases such as diabetes and cancer, pregnancy, and any other pathology that produces neck pain other than that specified in the objective of the study

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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