Combined Effect Of Cranial And Cervical Mobilization In Patients With CGH

NCT ID: NCT05697445

Last Updated: 2023-02-01

Study Results

Results pending

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.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-28

Study Completion Date

2023-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

* The purposes of this study are:
* To investigate the combined effect of cranial and cervical mobilization in patient with cervicogenic headache and there effect on :

1. Perceptive neck pain intensity
2. Perceptive headache intensity
3. pain by pressure
4. frequency of headache episodes
5. duration of headache episodes
6. Medications uptakes

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.

Cervicogenic Headache

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Cranial Mobilization and Exercises Group

Group Type EXPERIMENTAL

Mobilization Techniques

Intervention Type OTHER

Combination of Cranial and Cervical Mobilization for Cervicogenic headache Patients treatment

Conventional Treatment

Intervention Type OTHER

Cervicogenic headache exercises

Exercises Group

Group Type ACTIVE_COMPARATOR

Conventional Treatment

Intervention Type OTHER

Cervicogenic headache exercises

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Mobilization Techniques

Combination of Cranial and Cervical Mobilization for Cervicogenic headache Patients treatment

Intervention Type OTHER

Conventional Treatment

Cervicogenic headache exercises

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* pain originating at the neck and radiating to oculo-frontal-temporal regions.
* symptom unilaterally.
* symptom provocation through cervical movement and/or awkward cervical postural.
* symptom provocation through external pressure application through palpation to associated posterior cervical spine segments with resultant symptom reproduction.
* possible ipsilateral shoulder and/or arm pain of vague reference.
* 15 or more headache episodes per month
* No history of cervical operation or any disease that result in headache as colities -All patients will sign the informed consent before joining the study.

Exclusion Criteria

* Headache not of cervical origin
* Headache with autonomic involvement, dizziness, or visual disturbance
* Congenital conditions of the cervical spine
* It is of primary concern to exclude serious or life-threatening pathology such as :
* cranial tumors.
* Meningitis.
* sub-arachnoid hemorrhage.
* carotid artery,vertebral artery dissection.
* History of cervical operation or any disease that result in headache as colitis
* Age less than 18 or more than 40 years
* chronic maxillary sinusitis
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mennat Allah Hussien Mahmoud Mouhamed

physical therapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Mennat Allah Hussien Mahmoud

Role: CONTACT

+2001090122467

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Mobilization In CGH Treatment

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.