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Effectiveness of the Treatment of Tension-type Headache With Manual and Manipulative Therapy

U

University of Valencia

Status

Completed

Conditions

Tension-type Headache

Treatments

Other: Manual Therapy
Other: placebo treatment

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Background. Tension-type headache (TTH) is the most common form of primary headache and it is a real problem for the subjects suffering from it. Until now, physiotherapy treatments have included different techniques combined together, without establishing which of them is more effective.

Objective. The purpose of this study is to know the effectiveness of manipulative and manual therapy treatments, with regard to pain perception and neck mobility in patients with tension-type headache.

Methods: A double-blind, randomized clinical trial was conducted, with 84 patients diagnosed with tension-type headache, divided into three treatment groups -manual therapy, manipulative therapy, and a combination of both techniques-, and a placebo control group. Four treatment sessions were administered during four weeks, with post-treatment assessment, and follow-up at one month. Cervical ranges of motion were assessed (CROM device), as well as pain perception (McGill Pain Questionnaire), and frequency and intensity of headaches (weekly register).

Enrollment

84 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects aged between 18 and 65 years

  • Diagnosis of frequent ETTH and CTTH

  • Having headache episodes on more than 1 day per month

  • Headache episodes lasting from 30 minutes to 7 days

  • Headaches having at least 2 of the following characteristics:

    • Bilateral location of pain
    • Pressing non pulsating quality
    • Mild or moderate intensity
    • Not aggravated by physical activity
  • Sufferers may present photophobia, phonophobia, nausea or vomiting

  • Headache may be associated with pericranial tenderness

  • Suffering from TTH for over 3 months

  • Subjects being under pharmacological control

Exclusion criteria

  • Patients with infrequent ETTH, and patients with probable TTH in its frequent and infrequent forms.

    • Headache that is aggravated by head movements.
    • Metabolic or musculoskeletal disorders with symptoms similar to headache
    • Previous neck trauma
    • Vertigo, dizziness, arterial hypertension.
    • Joint stiffness, arteriosclerosis or advanced degenerative osteoarthritis
    • Patients with heart devices
    • Patients in process of pharmacological adaptation
    • Excessive emotional tension
    • Neurological disorders
    • Laxity of neck soft tissues
    • Radiological alterations
    • General hypermobility or hyperlaxity
    • Joint instability
    • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Triple Blind

84 participants in 4 patient groups, including a placebo group

Manual therapy
Experimental group
Description:
Manual therapy of Suboccipital soft tissue Inhibition treatment aims to release the suboccipital muscle spasm that maintains the occiput-atlas-axis joint dysfunction.
Treatment:
Other: Manual Therapy
Other: Manual Therapy
Other: Manual Therapy
Occiput-atlas-axis joint manipulation
Experimental group
Description:
Is bilaterally administered. The aim of restoring the mobility of joints between occiput, atlas and axis, which enables to correct a global joint dysfunction
Treatment:
Other: Manual Therapy
Other: Manual Therapy
Other: Manual Therapy
Combined treatment
Experimental group
Description:
The group receiving combined treatment received the two previous techniques exactly with the same sequence.
Treatment:
Other: Manual Therapy
Other: Manual Therapy
Other: Manual Therapy
Control group
Placebo Comparator group
Description:
Control group not receive treatment and stayed in this position for 10 minutes
Treatment:
Other: placebo treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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