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

U

University of Sao Paulo

Status

Unknown

Conditions

Myofascial Pain Syndrome
Neck Pain

Treatments

Other: Ultrasound
Other: Diadynamic currents
Other: Kinesiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT01869283
U1111-1143-4456

Details and patient eligibility

About

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%.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 59 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 4 patient groups

Kinesiotherapy group
Experimental group
Description:
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.
Treatment:
Other: Kinesiotherapy
kinesiotherapy + static ultrasound group
Experimental group
Description:
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.
Treatment:
Other: Kinesiotherapy
Other: Ultrasound
kinesiotherapy + diadynamic currents group
Experimental group
Description:
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.
Treatment:
Other: Kinesiotherapy
Other: Diadynamic currents
Control group
No Intervention group
Description:
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.

Trial contacts and locations

1

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Central trial contact

Rinaldo Guirro, PhD

Data sourced from clinicaltrials.gov

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