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Diacutaneous Fibrolysis, Effects on Tension Type Headache

Not Applicable
Completed
Conditions
Tension-Type Headache
Interventions
Device: Diacutaneous Fibrolysis
Registration Number
NCT03056131
Lead Sponsor
Sara Cabanillas Barea
Brief Summary

Tension Type Headache (TTH) is a frecuent type of headache disorder (about 1 person in 5 worldwide). Individuals with TTH typically present pericraneal tenderness and an increased cervical muscle tone.

The most common treatment in primary care consists mainly on analgesic medication. However, different techniques of manual therapy have been shown to be effective in the treatment of these patients. Diacutaneous fibrolysis shows clinical benefits in relieving symptoms of tension type headache, but there is no scientific evidence that analyzes this effects.

The hypothesis of this study was that adding treatment with diacutaneous fibrolysis to the usual conservative treatment has beneficial effects on different variables of the headache.

The aim of the study was to assess the effect of diacutaneous fibrolisis on intensity, frequency, duration of headache and cervical function in patients with tension type headache.

A randomized controlled clinical trial has been designed to evaluate the effectiveness of diacutaneous fibrolysis technique compared to usual general practicioner care in patientes with tension type headache.

The study protocol has been approved by the Clinical Research Ethics Committee from the Aragon Community and all patients provided written consent.

Eighty-two people with clinical diagnosis of TTH were randomized into a intervention group or a control group. Intervention group received three sessions of Diacutaneous Fibrolysis, while control group was advised to maintain their usual pharmacologic treatment. Pain intensity (VAS), frecuency, location, cervical range of motion, head forward position and pressure pain thresholds (PPTs) were measured at baseline, postintervention, and 1 month follow-up after treatment. The Spanish version of the HIT-6 Questionnaire was used to measure disability/function at baseline and follow-up.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
82
Inclusion Criteria
  • Diagnosis of Tension-Type Headache according to the criteria of ICDH-III.
Exclusion Criteria
  • Currently undergoing physiotherapy treatment for headache
  • Modification of pharmacological treatment in the last month
  • Presence of red flags

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Diacutaneous Fibrolysis TreatmentDiacutaneous Fibrolysis-
Primary Outcome Measures
NameTimeMethod
Change in Pain Intensity10 days

Visual Analog Scale (VAS)

Secondary Outcome Measures
NameTimeMethod
Dissability1 month

HIT-6 Questionnaire

Change in Pain Frequency10 days
Pericraneal tenderness10 days

Manual assessment

Cervical Range of motion10 days

Cervical Range of Motion (CROM)

Pressure Pain Threshold10 days

Pressure algometry

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