NCT05939557

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2015

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2015

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2015

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2015

Completed
8 years until next milestone

First Submitted

Initial submission to the registry

June 10, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 11, 2023

Completed
Last Updated

July 11, 2023

Status Verified

June 1, 2023

Enrollment Period

1 month

First QC Date

June 10, 2023

Last Update Submit

June 30, 2023

Conditions

Keywords

Cervicalgiacinta de kinesioTécnica de Jonesfisioterapiapuntos de activación.

Outcome Measures

Primary Outcomes (4)

  • 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

    time 0, after 4 weeks of treatment, and at the 2-week follow-up

  • 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

    time 0, after 4 weeks of treatment, and at the 2-week follow-up

  • 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

    time 0, after 4 weeks of treatment, and at the 2-week follow-up

  • 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.

    time 0, after 4 weeks of treatment, and at the 2-week follow-up

Study Arms (3)

Jones technique group

EXPERIMENTAL

Performs Jones technique 12 participants.

Procedure: Jones technique

kinesio tapping group

EXPERIMENTAL

Performs kinesiotape 14 participants.

Device: Kinesiotape

combined therapy group

EXPERIMENTAL

Performs Jones technique and kinesiotape 12 participants.

Procedure: Jones techniqueDevice: Kinesiotape

Interventions

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)

Jones technique groupcombined therapy group

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

combined therapy groupkinesio tapping group

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neck Pain

Interventions

Athletic Tape

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

BandagesEquipment and SuppliesOrthotic DevicesOrthopedic EquipmentSurgical Equipment

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
PHD

Study Record Dates

First Submitted

June 10, 2023

First Posted

July 11, 2023

Study Start

March 1, 2015

Primary Completion

April 1, 2015

Study Completion

June 30, 2015

Last Updated

July 11, 2023

Record last verified: 2023-06

Data Sharing

IPD Sharing
Will not share