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The Effects of Dry Needling on the Superficial Neck Musculature

U

University of Valladolid (UVA)

Status

Completed

Conditions

Neck Pain

Treatments

Other: Dry needling
Other: Sham dry needling
Other: Electrotherapy + therapeutic exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT04060004
1.0 14/12/2018

Details and patient eligibility

About

The term myofascial pain refers to the existence of myofascial trigger points (MTP), which are defined as hypersensitive points in a tense band of skeletal muscle, which can cause referred pain or autonomous phenomena.

To address the treatment of myofascial trigger points, conservative and invasive techniques have been proposed. Dry needling is one of the invasive techniques that have been shown to be effective in improving pain and function in patients with myofascial trigger points.

This trial aims to analyse the effectiveness of dry needling in patients with myofascial neck pain.

Full description

The main objective of the study is to analyze the effects of dry needling on the superficial neck musculature in patients with chronic myofascial neck pain in terms of pain, functional capacity, mobility, psychosocial variables and motor control compared with both sham dry needling group and control group.

In addition, a secondary objective is to analyze the relationships between the psychosocial variables and the results obtained in the variables analyzed in the patients belonging to the three groups.

For this purpose the investigators conduct a randomized controlled trial double-blind. Patients included are randomized into 3 groups. One receives dry needling, another one receives sham dry needling, and the last one is a control group.

The hypothesis of this study is that patients in the real dry needling group will improve more compared to patients in the sham dry needling group and the control group.

Enrollment

50 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with myofascial neck pain
  • Presence of at least one active myofascial trigger point on the superficial neck musculature
  • Neck pain of at least 3 months
  • Age 18-70
  • Pain intensity between 20 and 100 mm in the Analog Visual Scale
  • Neck disability index (NDI) greater than or equal to 15 points
  • Spanish speakers
  • Patients who do not present contraindications for the use of dry needling (anticoagulants, nickel allergy or belenophobia)
  • Patients who have not received physiotherapy or pharmacological treatment for neck pain for the last three months

Exclusion criteria

  • History of cervical trauma
  • Cervical spine surgery
  • Vertebral fracture
  • Cervical pain associated with whiplash
  • Red flags (tumor, metabolic disorders or rheumatoid arthritis)
  • Inflammatory lesion in the neck region
  • Pregnancy
  • Fibromyalgia diagnosis
  • Neck pain associated with radiculopathy
  • Patients pending legal litigation
  • Psychiatric pathology diagnosis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 3 patient groups, including a placebo group

Control group
Other group
Description:
Electrotherapy + therapeutic exercise
Treatment:
Other: Electrotherapy + therapeutic exercise
Experimental group 1
Experimental group
Description:
Electrotherapy + therapeutic exercise + dry needling
Treatment:
Other: Dry needling
Other: Electrotherapy + therapeutic exercise
Experimental group 2
Placebo Comparator group
Description:
Electrotherapy + therapeutic exercise + sham dry needling
Treatment:
Other: Sham dry needling
Other: Electrotherapy + therapeutic exercise

Trial contacts and locations

1

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Central trial contact

Ricardo Medrano de la Fuente, MSc

Data sourced from clinicaltrials.gov

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