Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
20 participants
INTERVENTIONAL
2025-06-01
2025-10-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
the Effect of Reflexology in Migraine Patients
NCT06828315
The Effect of Connective Tissue Massage in Patients With Migraine
NCT04171362
The Effect of Two Different Massages on Migraine
NCT05452330
The Effectiveness of Cervical Kinesio Taping in Migraine
NCT06203678
Effect of Acupressure-Ice Message on Primary Dysmenorrhea
NCT06578013
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Control
No treatment other than medication will be given for migraine.
No interventions assigned to this group
Experimental
Reflexology massage will be applied twice a week for 30 minutes per session, for a total of 10 sessions.
Reflexology Massage
Reflexology massage will be applied twice a week for 30 minutes per session, for a total of 10 sessions. The treatment will begin by relaxing the ankle with a few passive movements. Reflexology massage will be applied to the right foot first and then to the left foot.
Target Areas to be Applied to the Right Foot: Brain, Pineal, Hypophysis, Hypothalamus and Thalamus, Temples, Eye area and Optic nerve, Ear area, Middle ear and Balance point, Neck.
Other areas to be applied to the right foot: Thyroid and Parathyroid, Lung, Liver, Face area, Speech center and Thymus, Teeth, Diaphragm, Vertebra, Extremities.
Areas to be applied to the left foot: Kidney, Diaphragm, Intestines, Neck, Vertebra, Extremities.
The session is completed from the left foot by applying to the lymph inlet, lymph channel and diaphragm from both feet.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Reflexology Massage
Reflexology massage will be applied twice a week for 30 minutes per session, for a total of 10 sessions. The treatment will begin by relaxing the ankle with a few passive movements. Reflexology massage will be applied to the right foot first and then to the left foot.
Target Areas to be Applied to the Right Foot: Brain, Pineal, Hypophysis, Hypothalamus and Thalamus, Temples, Eye area and Optic nerve, Ear area, Middle ear and Balance point, Neck.
Other areas to be applied to the right foot: Thyroid and Parathyroid, Lung, Liver, Face area, Speech center and Thymus, Teeth, Diaphragm, Vertebra, Extremities.
Areas to be applied to the left foot: Kidney, Diaphragm, Intestines, Neck, Vertebra, Extremities.
The session is completed from the left foot by applying to the lymph inlet, lymph channel and diaphragm from both feet.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being diagnosed with migraine by a neurologist according to the International Headache Society (IHS) criteria
* Volunteering to participate in the study
* Being able to read and write
* Not having entered menopause
Exclusion Criteria
* History of cervical or cranial surgery
* Irritation or ulceration on the skin area to be reflexologized
* Receiving non-drug migraine treatment (acupuncture, dry needle, etc.)
* Those who have received physiotherapy at least 6 months ago
* Presence of diabetic foot
* Open wounds on the foot
* Pregnant individuals or individuals who become pregnant during the study
18 Years
45 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Karabuk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tarik Ozmen
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Karabuk University
Karabük, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KBU-FTR-2025-2178
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.