Clinical trial Recruiting at 1 site Interventional Ages 45 to 65 Women only

Manual therapy for tension-type headache in premenopausal and menopausal women

Official title: Comparison of the Effect of Manuel Therapy on Tension Type Headache in Menopausal and Premenopasual Women

Run by Necmettin Erbakan University · NCT07477483 · Data updated 2026-11-12

We will test whether manual therapy can reduce pain and improve function in premenopausal and menopausal women with tension-type headache.

More Tension-Type Headache trials

Quick facts

Study typeInterventional
Ages45 Years to 65 Years
SexWomen only
Enrollment50 (estimated)
SponsorNecmettin Erbakan University
Academic / other
Locations1 site (Konya, Konya)
StatusRecruiting
StartedOctober 1, 2025
Main results expectedMay 2026
Study endsMay 2026
Registry record updatedMay 20, 2026
Trial IDNCT07477483 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are women aged 45–65 with a clinical diagnosis of tension-type headache, HIT-6 score ≥ 49, premenopausal or menopausal status, able to attend in-person sessions, and not using hormonal therapy or having prior cervical surgery or neurological disease.

Probably not a fit

Patients who are male, have other primary headache types (for example migraine), are on hormonal therapy, have a history of cervical surgery or neurological disease, are pregnant, or cannot attend treatment sessions are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will apply manual therapy (soft tissue techniques, cervical mobilization, and therapeutic exercises) to women aged 45–65 diagnosed with tension-type headache and compare responses between premenopausal and menopausal participants. Outcomes measured before and after the intervention include headache intensity (VAS), headache-related disability (HIT-6), pressure pain threshold (algometer), cervical range of motion (goniometer), sleep quality (PSQI), and health-related quality of life (SF-36). Participants must meet inclusion criteria such as HIT-6 ≥ 49 and must not be using hormonal therapy or have a history of cervical surgery or neurological disease. All treatments and assessments are delivered in person at Necmettin Erbakan University in Konya, Turkey.

Why it matters

Potential benefit: If successful, the approach could lower headache pain and related disability and improve sleep and quality of life for women with tension-type headache.

How similar studies have gone: Previous trials of manual therapy and neck-targeted exercises have shown modest reductions in tension-type headache pain and frequency, but direct comparisons by menopausal status are largely novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female participants aged between 45 and 65 years.
* Diagnosis of tension-type headache.
* Premenopausal or menopausal status.
* HIT-6 score of 49 or higher.
* Willingness to participate in the study.

Exclusion Criteria:

* Use of hormone therapy.
* History of cervical surgery.
* History of neurological disease.
* Pregnancy.
* Inability to understand questionnaire forms.
* Failure to attend treatment sessions.

Where it's running

  • Necmettin Erbakan Univesity Faculty of Health Sciences
    Konya, Konya, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Neslihan Altuntaş Yılmaz, PhD — Necmettin Erbakan University
  • Study coordinator: Ayça Seda Yıldırımer, PT, MSc
  • Email: aycaseda29@gmail.com
  • Phone: +90 507 409 08 99

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.