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NCT05493098
Effectiveness of Dry Needling in People With Episodic Tension-type Headache
NA trial testing dry needling in Episodic Tension-type Headache in 36 participants. Status unknown.
30 December 2023
Quick facts
| Lead sponsor | Iran University of Medical Sciences |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 36 |
| Start date | 30 June 2023 |
| Primary completion | 30 December 2023 |
| Estimated completion | 30 December 2023 |
Drugs / interventions tested
- dry needling
- sham (placebo) dry needling:
Conditions studied
- Episodic Tension-type Headache — all drugs for Episodic Tension-type Headache →
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.
Verify or expand the search:
- PubMed search for NCT05493098
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Other Iran University of Medical Sciences trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05493098 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Iran University of Medical Sciences
- Last refreshed: 16 February 2023
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