[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100569063":3},{"organization":4,"armGroups":7,"interventions":23,"overallOfficials":11,"centralContacts":36,"locations":11,"responsibleParty":42,"collaborators":11,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":11,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":11,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":11,"overallStatus":67,"whyStopped":11,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":73,"leadSponsor":75,"locationsCount":11},{"fullName":5,"class":6},"Cairo University","OTHER",[8,14,18],{"label":9,"type":10,"description":11,"interventionNames":12},"Group A (Dry needling): The 15 patients will receive three dry needling sessions per week for four","EXPERIMENTAL",null,[13],"Other: Group A (Dry Needling)",{"label":15,"type":10,"description":11,"interventionNames":16},"Group B (Dry cupping): The 15 patients will receive three dry cupping sessions per week for four we",[17],"Other: Group B (Dry cupping)",{"label":19,"type":20,"description":11,"interventionNames":21},"Group C (control): The 15 patients will receive standard exercise three sessions per week for four w","ACTIVE_COMPARATOR",[22],"Other: Group C (control)",[24,28,32],{"type":6,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"Group A (Dry Needling)","The patient will receive dry needling on suboccipital, upper trapezius and SCM muscles with conventional therapy 3 sessions per week for 4 weeks.",[9],{"type":6,"name":29,"description":30,"armGroupLabels":31,"otherNames":11},"Group B (Dry cupping)","Patients will receive dry cupping on suboccipital, upper trapezius and SCM muscles weeks with conventional therapy 3 sessions per week for 4 weeks.",[15],{"type":6,"name":33,"description":34,"armGroupLabels":35,"otherNames":11},"Group C (control)","will receive standard exercise three sessions per week for four weeks. This standard regimen consists of the same exercises as group A and B.",[19],[37],{"name":38,"role":39,"phone":40,"phoneExt":11,"email":41},"Mariam samara Shahen, Demonstrator","CONTACT","+201024909968","msamara@horus.edu.eg",{"type":43,"investigatorFullName":44,"investigatorTitle":45,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"PRINCIPAL_INVESTIGATOR","Mariam Samara Elsaeed Shahen","Demonstrater","100569063","dry-needling-versus-dry-cupping-on-pain-and-disability-in-cervicogenic-headache-patients-100569063",false,"NCT06689371","Dry Needling Versus Dry Cupping on Pain and Disability in Cervicogenic Headache Patients","Inclusion Criteria:\n\n* The patients will be included in our study if they meet the following criteria:\n\n  * Age between 25-45 years old for both genders.\n  * No physiotherapy intervention for the last three months.\n  * Intermittent headaches of varying duration and pain level at the rate of one headache per week for greater than 2 months.\n  * Ipsilateral neck, shoulder, or arm pain.\n  * Provocation of usual head pain by neck movement, sustained awkward neck positions or external pressure over the upper cervical or occipital region on the symptomatic side.\n  * Limited neck ROM \\> 10 degrees confirmed by a positive Flexion Rotation Test.\n  * Active trigger points (TrPs) within the suboccipital, upper trapezius or sternocleidomastoid muscles.\n\nThe diagnosis of active TrPs will be based on the major criteria proposed by):\n\n* Presence of a palpable taut band in a skeletal muscle\n* presence of a hypersensitive point in the taut band\n* local twitch response elicited by the snapping palpation of the taut band\n* reproduction of the referred pain in response to compression\n* patient recognition of the referred pain as a familiar symptom\n\nExclusion Criteria:\n\n* The patients will be excluded if they have:\n\n  * Cervical radiculopathy.\n  * History of neck, shoulder trauma or surgery.\n  * Physical therapy intervention in the neck and shoulder region in the previous 3 months.\n  * Vertebrobasilar insufficiency or vestibular dysfunctions.\n  * Evidence of cognitive deficits.\n  * Presence of any needle contraindication.\n  * Presence of any cupping contraindication.",true,"ALL","25 Years","45 Years",{"count":57,"type":58},45,"ESTIMATED","INTERVENTIONAL",[61],"NA","This study aims to compare the added effects of dry needling and dry cupping to conventional physical therapy on headache pain intensity, headache frequency, headache duration, upper cervical range of motion, and disability levels in patients with cervicogenic headache.\n\nIt will be assumed that:\n\n* All patients will follow all the given instructions strictly during the study duration, regarding the assessment and the treatment procedure.\n* All participants will be evaluated under the same environmental conditions.",[64,65,66],"Dry Needling","Dry Cupping","Cervicogenic Headache","NOT_YET_RECRUITING","2024-11-13",{"date":70,"type":71},"2024-11-14","ACTUAL",{"date":68,"type":58},{"date":74,"type":58},"2025-02-01",{"name":5,"class":6}]