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Suboccipital Inhibition in Tension Headache

Suboccipital Inhibition in Tension Headache

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04376125
Enrollment
30
Registered
2020-05-06
Start date
2019-02-01
Completion date
2020-06-30
Last updated
2020-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tension Headache

Keywords

tension headache, suboccipital inhibition

Brief summary

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

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

Interventions

OTHERSuboccipital inhibition in tension headache

Deep maneuver of myofascial induction in the suboccipital muscles

Sponsors

Sanidad de Castilla y León
CollaboratorOTHER
Universidad de León
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* pathology tension headache associated with cervicalgia

Exclusion criteria

* pathology of nervous system

Design outcomes

Primary

MeasureTime frameDescription
Change in Visual Analogue Scale for Painimmediately before starting the intervention and after the last session of the intervention, that is, 2 weeks from the starta continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, usually 10 centimeters (100 mm) in length, anchored by 2 verbal descriptors, one for each symptom extreme: no pain (score of 0) and worst imaginable pain (score of 10)

Secondary

MeasureTime frameDescription
Change in Six-item Headache Impact Textimmediately before starting the intervention and after the last session of the intervention, that is, 2 weeks from the startA global measure of adverse headache impact. The final HIT-6 score is obtained from simple summation of the six items and ranges between 36 and 78, with larger scores reflecting greater impact.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026