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NCT05493098

Effectiveness of Dry Needling in People With Episodic Tension-type Headache

Status unknown NA Last updated 16 February 2023
What this trial tests

NA trial testing dry needling in Episodic Tension-type Headache in 36 participants. Status unknown.

Timeline
30 June 2023
Primary endpoint
30 December 2023
30 December 2023

Quick facts

Lead sponsorIran University of Medical Sciences
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment36
Start date30 June 2023
Primary completion30 December 2023
Estimated completion30 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

Iran University of Medical Sciences

Who can join

Adults 20 to 50, any sex, with Episodic Tension-type Headache. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Tension-type headache is a widespread disorder, with a lifetime prevalence in the general population ranging between 30% and 78%. Tension-type headache also places a financial burden on society and individuals. Myofascial pain can reduce the range of motion and patterns of muscle activation and play an important role in tension-type headache. Based on the previous studies, dry needling can reduce local and referred pain, increase range of motion and improve patterns of muscle activation in patients with myofascial pain syndrome. The effectiveness of dry needling in patients with tension-type headache is not fully known. Objective: The aim of this study will be to investigate the effectiveness of dry needling on pain, active range of motion, functional disability, and frequency of headache in patients with episodic tension-type headache. Method: This study will be a double-blind randomized controlled trial. Thirty-six patients with episodic tension-type headache will be randomly divided into two groups: the experimental group (dry needling and routine physical therapy) and the control group (sham dry needling and routine physical therapy). The primary outcomes will be pain intensity and active range of motion of the craniocervical region. Functional disability and frequency of headache will be considered secondary outcomes. Outcomes will be assessed before and one week after the intervention.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of dry needling

Trials testing the same drug.

Other Iran University of Medical Sciences trials

Trials by the same sponsor.

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Data sources for this page

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