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Effectiveness of the Dry Needling Approach in Patients With Tension-Type Headache

U

University of Zaragoza

Status

Completed

Conditions

Tension-Type Headache
Dry Needling

Treatments

Other: Dry Needling

Study type

Interventional

Funder types

Other

Identifiers

NCT06108180
RAT 2023-195

Details and patient eligibility

About

Randomized Single-Blind Clinical Trial in which the treatment will be administered through 3 sessions of dry needling in the cervical, cranial, and facial musculature in patients with frequent and chronic tension-type headache.

Enrollment

32 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with a diagnosis of tension headache according to IHS

Exclusion criteria

  • Documented major trauma through medical history in the cervical area and/or recent surgery.
  • Pregnancy.
  • Generalized pain.
  • Inflammatory, hormonal, or neurological disorders.
  • Tendon disorders in the upper extremities.
  • Severe psychiatric illnesses.
  • Inability to complete the form in Spanish.
  • Having a pacemaker (due to the use of equipment with magnetic sensors).
  • Specific contraindications to invasive or conservative physiotherapy (infection, fever, hypothyroidism, wounds in the puncture area, metal allergies, cancer, systemic diseases, or belonephobia).
  • Having received physiotherapy treatment for the condition in the past month.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Dry Needling group
Experimental group
Treatment:
Other: Dry Needling
Control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Sofía Monti

Data sourced from clinicaltrials.gov

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