Actively Recruiting

Phase Not Applicable
Age: 45Years - 65Years
FEMALE
NCT07477483

Effect of Manuel Therapy on Tension Type Headache in Menopausal and Premenopasual Women

Led by Necmettin Erbakan University · Updated on 2026-03-17

50

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effectiveness of manual therapy in women with tension-type headache and to compare treatment outcomes between menopausal and premenopausal women. Hormonal changes occurring during menopause may influence pain perception and headache characteristics. Participants diagnosed with tension-type headache will receive manual therapy interventions. Headache intensity, headache-related disability, pressure pain threshold, cervical range of motion, sleep quality, and quality of life will be evaluated before and after treatment using validated assessment tools. The results are expected to contribute to physiotherapy approaches in women experiencing tension-type headache during different hormonal periods.

CONDITIONS

Official Title

Effect of Manuel Therapy on Tension Type Headache in Menopausal and Premenopasual Women

Who Can Participate

Age: 45Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged between 45 and 65 years
  • Diagnosed with tension-type headache
  • Premenopausal or menopausal status
  • Headache Impact Test (HIT-6) score of 49 or higher
  • Willing to participate in the study
Not Eligible

You will not qualify if you...

  • Use of hormonal therapy
  • History of cervical surgery
  • History of neurological disease
  • Pregnancy
  • Inability to understand questionnaires
  • Failure to attend treatment sessions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Necmettin Erbakan Univesity Faculty of Health Sciences

Konya, Konya, Turkey (Türkiye), 42090

Actively Recruiting

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Research Team

A

Ayça Seda Yıldırımer, PT, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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