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Use of Low Level Laser Therapy on Acupuncture points in patients with Chronic Tensional Headache in university students

Analysis of the analgesic effect of Low Level Laser Therapy in Chronic Tension Headache using Acupuncture points and its positive effects on the quality of life of students of the State University of Western Paraná

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9yddrg
Enrollment
Unknown
Registered
2019-08-12
Start date
2019-06-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Tension headache

Interventions

Use of the low level laser therapy with 30mW power, 660 nanometers wavelength, 10J/cm² energy density, 0.06 cm² spot area and 20 seconds application time at each of the six acupuncture points. The poi
when opening the thumb and index finger, in the middle of the line between the junction of the first and second metacarpal bone, the midpoint of the palm edge, or when closing the hand, between the fi
when bending the elbow, in the radial depression at the end of the cubital line. c) Schenmen (C7): on the ulnar side of the wrist, on the radial side of the flexor carpal ulnar muscle, behind the pisi
Device
Radiation
E02.594.540

Sponsors

Universidade Estadual do Oeste do Paraná (UNIOESTE)
Lead Sponsor
Universidade Estadual do Oeste do Paraná (UNIOESTE)
Collaborator

Eligibility

Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Individuals with chronic tension headache; who are not undergoing any type of treatment; men and women; who are between 18 and 30 years of age; and who are Universidade Estadual do Oeste do Paraná scholars will be included

Exclusion criteria

Exclusion criteria: Individuals who use medication and who have any complications in relation to laser treatment at acupuncture points will be excluded

Design outcomes

Primary

MeasureTime frame
Questionnaire HIT-6 (Headache Impact Test) with an increasing score indicating greater impact of headache on the individual's life. Evaluations will occur prior to the first intervention and at the end of the first intervention (after the third intervention). At the end of the protocol, it is expected to obtain a significant reduction in the score of the aforementioned questionnaire

Secondary

MeasureTime frame
Visual Analogue Pain Scale (VAS), with marking on a 100 mm straight line, in which 0 mm represents no pain and 100 mm the maximum pain imaginable, the level at which the volunteer evaluates his pain at the time of evaluation. These evaluations will follow the evaluation of the Headach Impact test

Countries

Brazil

Contacts

Public ContactGladson Bertolini

Universidade Estadual do Oeste do Paraná (UNIOESTE)

gladson_ricardo@yahoo.com.br+55-045-32207344

Outcome results

None listed

Source: REBEC (via WHO ICTRP)