Suboccipital Inhibition in Tension Headache

NCT ID: NCT04376125

Last Updated: 2020-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-01

Study Completion Date

2020-06-30

Brief Summary

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The researchers will carry out a randomized experimental study. Participants in the experimental group will receive a treatment based on suboccipital inhibition technique in addition to conventional treatment. Participants in the control group will only receive the conventional treatment. The existence of significant differences in both groups will be analyzed.

Detailed Description

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Conventional therapy will consist of microwaves, interference currents, and manual therapy.

Conditions

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Tension Headache

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Suboccipital inhibition in tension headache

Two groups of patients suffering from tension headache associated with cervicalgia are selected.

The control group performs conventional therapy. The experimental group performs conventional therapy plus the technique of suboccipital inhibition

Group Type EXPERIMENTAL

Suboccipital inhibition in tension headache

Intervention Type OTHER

Deep maneuver of myofascial induction in the suboccipital muscles

study of results

We compared data from both groups

Group Type ACTIVE_COMPARATOR

Suboccipital inhibition in tension headache

Intervention Type OTHER

Deep maneuver of myofascial induction in the suboccipital muscles

Interventions

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Suboccipital inhibition in tension headache

Deep maneuver of myofascial induction in the suboccipital muscles

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* pathology tension headache associated with cervicalgia

Exclusion Criteria

* pathology of nervous system
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sanidad de Castilla y León

OTHER

Sponsor Role collaborator

Universidad de León

OTHER

Sponsor Role lead

Responsible Party

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Cristina Blanco Ortega

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Cristina Blanco Ortega, physiotherap

Role: PRINCIPAL_INVESTIGATOR

Universidad de León

Locations

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Cristina Blanco Ortega

León, , Spain

Site Status

Countries

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Spain

Other Identifiers

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71441538L

Identifier Type: -

Identifier Source: org_study_id

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