The Effects of Cervical Stabilization Exercise Training With Telerehabilitation in Individuals With Migraine
NCT ID: NCT05202171
Last Updated: 2022-01-21
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.
UNKNOWN
NA
40 participants
INTERVENTIONAL
2022-02-28
2023-06-30
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 Cervical Stabilization Training in Individuals With Migraine
NCT06991504
Cervical Stability and Body Awareness in Migraine
NCT07116590
Cervical Stabilization Training on Individuals With Headache
NCT05839496
Efficacy of Lumbar Motor Control Training in Treatment Of Patients With Cervicogenic Headache
NCT05952115
Effect of Stabilization Exercises in Individuals With Non-Specific Chronic Neck Pain.
NCT05369260
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
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise group
Exercise group will be performed cervical stabilization exercise training applied with telerehabilitation and standard treatment ( preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine) for 8 weeks
Cervical Stabilization Exercise
Exercise group will be performed cervical stabilization exercise training applied with telerehabilitation and standard treatment ( preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine) for 8 weeks
Standard treatment group
Standard treatment group will be given preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine for 8 weeks.
Standard treatment
standard treatment will include preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine for 8 weeks
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Cervical Stabilization Exercise
Exercise group will be performed cervical stabilization exercise training applied with telerehabilitation and standard treatment ( preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine) for 8 weeks
Standard treatment
standard treatment will include preventive/symptomatic oral drug therapy routinely in the clinic and suggestions for triggering factors in migraine for 8 weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* To be diagnosed with migraine by a neurologist according to International Headache Society criteria,
* Having at least 3 migraine attacks per month,
* Volunteering to participate in the study,
* Having the opportunity to access devices such as computers, phones and tablets with internet connection,
* Not having any problems that prevent cooperation and understanding
Exclusion Criteria
* Being pregnant,
* Being in the breastfeeding period,
* Having a history of trauma, fracture or surgery in the craniocervical region,
* Presence of concomitant neurological and/or inflammatory rheumatic disease
* Presence of serious psychiatric problems,
* History of malignancy,
* Changes in medical treatment during the study period,
* Receiving physiotherapy for the cervical region in the last 6 months
18 Years
55 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ankara Yildirim Beyazıt University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
seyda toprak celenay
associate professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Seyda Toprak Celenay
Role: PRINCIPAL_INVESTIGATOR
Ankara Yildirim Beyazıt University
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.
2022/01/8
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.