Talking therapies take on migraine pain
NCT ID NCT07802912
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether two types of talking therapy can help people with chronic migraine. One is standard cognitive behavioral therapy, and the other is a traditional Islamic psychotherapy that blends psychological methods with Islamic principles. Adults aged 18 to 40 with a neurologist-confirmed diagnosis of chronic migraine will receive either one of these therapies or continue with medication alone. Researchers will compare changes in migraine-related disability, emotional distress, and quality of life across the three groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cognitive Behavioral Therapy (CBT) and Traditional Integrated Islamic Psychotherapy (TIIP), both delivered as structured six-week psychological interventions
- What this could lead to
- If effective, these talking therapies could offer drug-free ways to reduce migraine-related disability and improve quality of life for people with chronic migraine.
- What could go wrong
- The trial is small and early, so results may not apply widely. Psychological therapies require time and effort, and they may not help everyone with chronic migraine.
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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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45 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Jul 2026
- 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 40 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: * Aged between 18 and 40 years, the band Chen et al. (2024) identify as carrying the heaviest global burden of migraine prevalence and disability. * A neurologist's diagnosis of chronic migraine established in accordance with International Headache Society criteria. * A MIDAS total of 21 or above, so that participants carried a clinically meaningful level of impairment and had room to improve (Stewart et al., 2001). * A score in the mild to moderate band on at least one DASS-21 subscale, since the study concerned migraine-associated distress rather than primary psychiatric disorder (Lovibond \& Lovibond, 1995). * A stable prophylactic medication regimen for at least one month before enrolment, with no change planned during the study, so that any shift in outcome could not be laid at the door of a change in drugs. * Both men and women were eligible, so that the sample resembled the clinical population rather than one gender. * At least primary-level education, sufficient to read and complete the self-report instruments independently. * Enough Urdu or English to engage with the intervention material. * Willingness to give written informed consent and to commit to the full schedule of six weekly sessions and both assessment appointments. * Residence in Gujranwala for the duration of the study and reachable by telephone, so that attendance could be monitored and attrition kept down. * Not receiving any other form of psychotherapy at enrolment, so that the effect of the study interventions could be isolated. Exclusion Criteria: Aged below 18 or above 40 years. * A diagnosed severe psychiatric disorder, including psychotic disorder, bipolar disorder, or severe major depressive disorder with active suicidality. * A score in the severe or extremely severe range on any DASS-21 subscale, or any indication of suicidal thinking. * A current need for intensive or immediate psychiatric treatment. * A substance use disorder within the preceding six months. Substance use and withdrawal are themselves recognised causes of headache under the International Classification of Headache Disorders (Headache Classification Committee of the International Headache Society, 2018) and independently raise scores on measures of depression, anxiety, and stress, so their inclusion would have confounded both the primary and the secondary outcomes. Six months was adopted because it maps onto the early remission specifier of the DSM-5-TR, under which someone who has met no criterion for a substance use disorder for at least three months but less than twelve is classified as in early remission (American Psychiatric Association, 2022), making it a recognised diagnostic boundary rather than an arbitrary line. * A neurological disorder other than migraine, such as epilepsy, brain tumour, or multiple sclerosis. * A serious medical condition likely to interfere with participation or to confound the outcomes. * Concurrent psychotherapy or enrolment in another intervention study. * Inability to give informed consent or to comply with the study procedures.
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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.
Contacts and locations
Locations
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GIFT University
Gujranwala, Punjab Province, 52250, Pakistan
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