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Clinical Trials/NCT01869283
NCT01869283UnknownNot Applicable

Effectiveness of Physical Therapy Treatments of Myofascial Trigger Points in Subjects With Neck Pain

University of Sao Paulo1 site in 1 country80 target enrollmentStarted: May 1, 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
80
Locations
1
Primary Endpoint
Pain

Study Overview

Brief Summary

Neck pain is a prevalent musculoskeletal dysfunction. Studies point that individuals with chronic pain have metabolic, vascular and electromyographic changes in trapezius muscle. Moreover, a common clinical sign in this muscle in subjects with neck pain is the presence of myofascial trigger points. These are related to the sensory, motor and autonomic changes, being defined as palpable nodules located in the taut band of skeletal muscle. In this context, the focus on treatment modalities stands out in the literature, however, other resources commonly used in clinical practice still lack scientific evidence. Therefore, the aim of this project is to evaluate the effectiveness of physiotherapy resources in the treatment of myofascial trigger points in the trapezius muscle of patients with neck pain. For such, volunteers with neck pain for more than 90 days, of both genders, aged between 18 and 59 years and bilateral myofascial trigger points in the upper trapezius will be randomized into the following groups: group 1 (kinesiotherapy, n = 20), group 2 (kinesiotherapy + static ultrasound, n = 20), group 3 (kinesiotherapy + diadynamic currents, n = 20) and group 4 (untreated control, n = 20). Volunteers will undergo ten sessions of treatment, being realized the following evaluations: surface electromyography, infrared thermography, numerical scale of pain assessment, algometry, Neck Disability Index and skin impedance. For data analysis, normality test will used to verify the data distribution and consistent statistical test for the appropriate comparisons within and between groups, and thus considered two factors in the comparisons, time and group. Will adopt a significance level of 5%.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 59 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •neck pain for more than 90 days
  • •aged 18 to 59 years
  • •presence of trigger points in the upper trapezius muscle

Exclusion Criteria

  • •history of trauma to the neck
  • •surgery in the head, face or neck
  • •herniated cervical
  • •degenerative diseases of the spine
  • •systemic diseases
  • •underwent physical therapy in the last three months
  • •analgesics, anti-inflammatories or muscle relaxants last week
  • •medical diagnosis of fibromyalgia
  • •body mass index (BMI) greater than 28 kg/m2
  • •signs and symptoms of depression

Arms & Interventions

Kinesiotherapy group

Experimental

The volunteer will be subjected to the following protocol: cervical traction, 3 sets of 1 minute, 30-second rest between sets; mobilization grade III postero-anterior on the spines processes of vertebrae C2 to C7, 10 oscillations for each vertebrae; myofascial release of the upper trapezius muscle, 3 sets of 1 minute for each side; static stretching of the upper trapezius muscle, 3 sets of 30 seconds, with an interval of 10 seconds between sets.

Intervention: Kinesiotherapy (Other)

kinesiotherapy + static ultrasound group

Experimental

Same protocol group kinesiotherapy + ultrasound on the trigger points of the upper trapezius muscle in a static way, with 1 MHz, continuous dose of 1.5 W/cm2, for 1.5 minutes.

Intervention: Kinesiotherapy (Other)

kinesiotherapy + static ultrasound group

Experimental

Same protocol group kinesiotherapy + ultrasound on the trigger points of the upper trapezius muscle in a static way, with 1 MHz, continuous dose of 1.5 W/cm2, for 1.5 minutes.

Intervention: Ultrasound (Other)

kinesiotherapy + diadynamic currents group

Experimental

Same protocol group kinesiotherapy + diadynamic currents, with negative electrode (7.0 x 7.0 cm) placed on the myofascial trigger point, while the positive electrode (7.0 x 7.0 cm) is placed between the shoulder blades. Will apply 4 minutes from the biphasic mode (DF) and 6-minute short period (CP), the first of which intesidade the sensory threshold and the second threshold motor, both bearable for the patient.

Intervention: Kinesiotherapy (Other)

kinesiotherapy + diadynamic currents group

Experimental

Same protocol group kinesiotherapy + diadynamic currents, with negative electrode (7.0 x 7.0 cm) placed on the myofascial trigger point, while the positive electrode (7.0 x 7.0 cm) is placed between the shoulder blades. Will apply 4 minutes from the biphasic mode (DF) and 6-minute short period (CP), the first of which intesidade the sensory threshold and the second threshold motor, both bearable for the patient.

Intervention: Diadynamic currents (Other)

Control group

No Intervention

The volunteers of this group will not be subjected to any form of treatment, was evaluated in three stages, as the other groups. It is noteworthy that, after the volunteer's participation, will be offered at the same physical therapy for myofascial pain.

Outcomes

Primary Outcomes

Pain

Time Frame: 3 years

Will be apply the following assessment tools: Neck Disability Index (assesses neck pain and disability), algometry (evaluates pressure pain threshold), and numerical scale of pain assessment (assesses pain intensity).

Secondary Outcomes

  • Cervical range of motion(3 years)
  • Skin temperature(3 years)
  • Muscle activity(3 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rinaldo Roberto de Jesus Guirro

Professor, PT, PhD

University of Sao Paulo

Study Sites (1)

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