Tension-type Headache Clinical Trial
Official title:
Effectiveness of a Global Manual Therapy Protocol vs Exercises With Foam Rolling for Tension Headache
Tension headache (CT) is the most frequent problem within the group of headaches, with a
prevalence of 30-78% of the population throughout its life. Regarding this pathology,
treatment with manual therapy has been studied a lot, observing the benefits of different
techniques separately in elements such as disability, impact or depression.
The "Foam Rolling" (FR) is an element widely used in sport that has been studied its
applications in terms of hip and knee flexibility after application in muscles such as the
quadriceps or hamstrings.
In this study the investigators recruited randomized subjects in three groups, one of
exercises with RF, another of a protocol of manual therapy (TM) techniques and one control
(CTR) with a placebo treatment. There will be 4 treatments, 1 per week, and the data will be
collected in 3 moments, pre-treatment, post-treatment and one month after treatment.
The investigators will evaluate aspects such as the average pain of headaches, the impact,
disability, quality of life, self-satisfaction and pain at the pressure of painful points of
the trapezius and suboccipital muscles.
Introduction Primary headaches occupy an important field in neurology consultations. Both
migraines and tension headaches are often self-treated by the patients themselves and for
some patients, headache is a true disease, constituting a symptomatology that can have
various etiologies, from severe to functional organics. Headache, when it becomes chronic,
becomes a serious problem for the patient with important repercussions on their quality of
life.
Objective. To evaluate the effectiveness of the application of the treatment by means of
manual therapy in patients with tension headache and to compare it with the application of
massage by means of a roll of foam manufactured for this purpose.
Methodology The study will be carried out in the Faculty of Physiotherapy of the Universitat
de València. An experimental, longitudinal and prospective design, controlled, randomized,
with 3 groups will be carried out.
Population. The sample will be formed by participants diagnosed with tension headache,
following the criteria established by the IHS.
Subjects with headache less than 15 days per month and other types of primary headache, as
well as those associated with drug abuse and those who do not meet the criteria established
by the IHS, will be excluded from the study.
Experimental treatment The patients will be randomly assigned to 3 different groups (one
group of treatment with manual therapy, one group that will receive massage and another group
of placebo control).
The treatment will last for 8 weeks (4 weeks of treatment and 4 weeks of follow-up). The 2
groups will be evaluated before treatment, at the end of this and in the follow-up (30 days
after treatment).
Evaluations
For the collection of data, a clinical interview with data referring to headache was designed
and the following evaluation instruments are included:
- Scale disability due to HDI Headache
- Impact of pain HIT-6
- Quality of life SF-36
- Visual Analog Scale (EVA)
- Algometry. Measurement of pain at pressure on spinous and transverse processes
- CROM. Cervical range
- QS. Body satisfaction questionnaire
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