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Online Yoga Added to Usual Care for Frequent Migraine

Tests an online Hatha yoga program added to usual medicine in adults with frequent migraine.

Plain-language title generated from the registry record
Registry title: Online Hatha Yoga Program as an Add-On Therapy for Episodic High-Frequency Migraine

Key facts

Where
Seville, SpainSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07694063, who can take part

Where in Spain

  • University Hospital Virgen del RocioSeville, SpainTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Seville
Trial code
NCT07694063
Record updated
9 July 2026
Original description
This randomized controlled trial aims to evaluate the effectiveness and feasibility of an online Hatha yoga program as an adjunct (add-on) therapy for patients with high-frequency episodic migraine. Participants will be randomly assigned to either an intervention group receiving a 12-week home-based online Hatha yoga program in addition to usual pharmacological treatment, or a control group receiving usual pharmacological care only. Outcomes include migraine frequency, pain intensity, functional disability, sleep quality, psychological symptoms, and adherence.Read full original descriptionShow less

A Randomized Controlled Trial of an Online Hatha Yoga Program as an Add-On Therapy for Episodic High-Frequency Migraine

This randomized controlled trial aims to evaluate the effectiveness and feasibility of an online Hatha yoga program as an adjunct (add-on) therapy for patients with high-frequency episodic migraine. Participants will be randomly assigned to either an intervention group receiving a 12-week home-based online Hatha yoga program in addition to usual pharmacological treatment, or a control group receiving usual pharmacological care only. Outcomes include migraine frequency, pain intensity, functional disability, sleep quality, psychological symptoms, and adherence.

Inclusion: Adults aged 18-65 years; Diagnosis of episodic high-frequency migraine according to ICHD criteria; Diagnosis confirmed by a neurologist; At least 1-year history of migraine; Receiving stable pharmacological treatment for ≥3 months before enrollment; Willing to maintain stable medication during the study; Ability to understand study procedures and complete assessments; Signed informed consent; Willingness to be randomized.

Exclusion: Use of more than one preventive migraine medication; Other significant neurological disorders; Severe psychiatric conditions affecting participation; Medical contraindications to moderate physical activity; Chronic migraine (≥15 headache days/month); Lack of Spanish language comprehension; Lack of internet access or digital skills for online intervention.

ClinicalTrials.gov NCT07694063