Ireland
--:--IST
Recruiting Not applicable

Basic Body Awareness Therapy in Individuals With Migraine

NCT07328685 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-02
Last updated
2026-05-22

Condition(s) studied

Migraine

Investigational drug(s) / intervention(s)

ExerciseStandart therapy

Exercise: Participants will receive body awareness therapy. The program will be administered over an eight-week period and will include exercises appropriate for the study population.

Standart therapy: Standard treatment will be in the form of individual information sessions lasting approximately 30 minutes for both groups. Brochures will be created for distribution to individuals.

Study summary

One biopsychosocial approach proven effective in headache treatment is basic body awareness therapy. This study was planned to evaluate the effectiveness of basic body awareness training and lifestyle recommendations in individuals diagnosed with migraine. Functional status will be assessed using the Migraine-Related Disability Assessment Scale (MIDAS), sleep quality using the Jenkins Sleep Scale (JUS), and quality of life using the Headache Impact Test. Assessment of functional status, sleep quality, and quality of life will be performed before treatment and after treatment (at the end of week 8).

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with migraine, * Experiencing at least 3 migraine attacks per month, * Between the ages of 18 and 55 and who volunteer to participate in the study. Exclusion Criteria: * History of secondary headaches, * Being pregnant, * Having any other neurological disease besides migraine, * Having other secondary headaches in addition to migraine, * History of malignancy, * Regularly practicing meditation, yoga, or mindfulness-based practices.

Primary outcome measure(s)

  • Pain Diary — Individuals will be asked to regularly complete a pain diary during the 4-week period before the program, during the program, and during the 4-week follow-up period after the training is completed.
    The severity, duration, and frequency of headaches during attacks will be recorded daily by the participants.

Trial sites (1)

FacilityCityRegionStatus
Hatay Mustafa Kemal University Antakya Hatay Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07328685 on ClinicalTrials.gov ↗ ← All trials in Turkey