Exercise, diet, and sleep: a new attack plan against chronic migraine?
NCT ID NCT07802860
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether an 8-week lifestyle program can reduce the burden of chronic migraine, a condition marked by headaches on at least 15 days per month. Adults aged 18 to 55 with chronic migraine will be randomly assigned to either the lifestyle program or a wait-list control group. The program includes supervised exercise, education on diet, stress, sleep, and social connections, plus peer support, all alongside their usual migraine medication. Researchers will track attack frequency, severity, disability, and markers of inflammation to see if lifestyle changes make a measurable difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- An 8-week comprehensive lifestyle intervention with supervised exercise, patient education, and peer support, addressing physical activity, diet, stress, sleep, substance use, and social connections.
- What this could lead to
- If it works, this could offer a drug-free add-on strategy to reduce migraine attacks and disability, improving daily life for people with chronic migraine.
- What could go wrong
- The trial is small (30 participants) and early, so results may not apply broadly. The intervention requires time and commitment, and its benefits beyond usual care are unproven.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Having been diagnosed with chronic migraine according to the ICHD-3 diagnostic criteria after a neurological examination by a Neurology Specialist * Not having a regular medication habit other than for migraine pain * No changes in current medication management during the study period * Being between 18-55 years of age Exclusion Criteria: * Having headache types other than chronic migraine * Having rheumatological diseases characterized by chronic widespread pain, such as fibromyalgia * Having neurological, orthopedic, or cardiovascular conditions that may prevent the individual from participating in exercise * Comorbid conditions other than migraine that are known to adversely affect cognitive functioning (e.g., traumatic brain injury, personality disorders, post-traumatic stress disorder, bipolar affective disorder, etc.) * Use of medications that may affect autonomic function * Receiving hormone replacement therapy * Receiving antihypertensive treatment * Having undergone botulinum toxin application within the last six months * Having undergone invasive procedures such as dry needling/injection within the last six months * Pregnancy * For female patients, being postmenopausal
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hacettepe University Faculty of Physical Therapy and Rehabilitation
Ankara, 06100, Turkey (Türkiye)
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