[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100617658":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":35,"locations":44,"responsibleParty":67,"collaborators":34,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":34,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":34,"enrollmentInfo":79,"targetDuration":34,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":47,"whyStopped":34,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"Palacky University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental Group: intervention with Dry Needling and Standard Rehabilitation)","EXPERIMENTAL","Participants in this group will receive standard outpatient rehabilitation therapy combined with Intervention: one dry needling intervention targeting trigger points in the masseter and temporalis muscles during the first treatment session. The rehabilitation program will include mobilization, soft tissue techniques, and targeted kinesiotherapy. Each participant will undergo ten outpatient rehabilitation sessions over five weeks (two sessions per week).",[13,14],"Procedure: Dry needling","Procedure: Standard rehabilitation",{"label":16,"type":17,"description":18,"interventionNames":19},"Control Group - Standard Rehabilitation","ACTIVE_COMPARATOR","Participants in this group will receive the same standard outpatient rehabilitation program as the experimental group, excluding the dry needling procedure. The therapy will include mobilization, soft tissue relaxation techniques, and specific exercises focused on improving temporomandibular joint mobility and reducing muscle tension",[14],[21,28],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Dry needling","One dry needling intervention targeting trigger points in the masseter and temporalis muscles during the first treatment session",[9],[27],"reflex injection therapy of Trigger Point",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"Standard rehabilitation","The therapy will include mobilization, soft tissue relaxation techniques, and specific exercises focused on improving temporomandibular joint mobility and reducing muscle tension.",[16,9],[33],"Standard Physical Rehabilitation Program",null,[36,41],{"name":37,"role":38,"phone":39,"phoneExt":34,"email":40},"Petr Konečný, Ph.D, M.D., assoc.prof.","CONTACT","+420604573931","petr.konecny@upol.cz",{"name":42,"role":38,"phone":34,"phoneExt":39,"email":43},"Dana Dvořáková, MSc.","dana.dvorakova01@upol.cz",[45],{"facility":46,"status":47,"city":48,"state":34,"zip":49,"country":50,"countryCode":34,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"Faculty of Health Sciences, Palacký University Olomouc, Czech Republic","RECRUITING","Olomouc","77900","Czechia",{"type":52,"coordinates":53},"Point",[54,55],17.25175,49.59552,{"lat":55,"lon":54},[58,60,61,64],{"name":59,"role":38,"phone":39,"phoneExt":34,"email":40},"PETR Konečný, Ph.D., M.D.; assoc.prof.",{"name":42,"role":38,"phone":39,"phoneExt":34,"email":43},{"name":62,"role":63,"phone":34,"phoneExt":34,"email":34},"PETR Konečný, Ph.D., MBA, assoc.prof.","PRINCIPAL_INVESTIGATOR",{"name":65,"role":66,"phone":34,"phoneExt":34,"email":34},"Dana Dvorakova, MSc.","SUB_INVESTIGATOR",{"type":63,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":34,"oldOrganization":34},"Petr Konecny","Associate Professor, Head of the Institute of Clinical Rehabilitation, Palacký University Olomouc","100617658","reflex-therapy-of-temporomandibular-dysfunctions-100617658",false,"NCT07321483","Reflex Therapy of Temporomandibular Dysfunctions","Evaluation of the Therapeutic Efficacy of Reflex Therapy Using Dry Needling in Patients With Functional Temporomandibular Pain Syndrome: A Prospective, Randomized, Controlled Pilot Study.","Inclusion Criteria:\n\n* Diagnosed with functional temporomandibular pain syndrome without structural temporomandibular joint damage.\n* Aged ≥18 years.\n* Stable health condition suitable for outpatient rehabilitation.\n* Willingness to participate and ability to follow the therapeutic protocol.\n\nExclusion Criteria:\n\n* Presence of degenerative, post-traumatic, or inflammatory changes in the temporomandibular joint.\n* Cognitive or psychiatric disorders limiting cooperation.\n* Lack of informed consent or non-compliance during treatment","ALL","18 Years",{"count":80,"type":81},100,"ESTIMATED","INTERVENTIONAL",[84],"NA","This study aims to evaluate the effectiveness of dry needling in patients with functional temporomandibular pain syndrome by comparing standard rehabilitation therapy alone with therapy combined with dry needling to reduce pain, improve jaw function and enhance quality of life.",[87],"Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders",[89,90],"headache; temporomandibular disorders; dry needling; rehabilitation therapy; pain; quality of life","temporomandibular disorders; dry needling; rehabilitation therapy; pain; quality of life","2025-12-28",{"date":93,"type":94},"2026-01-07","ACTUAL",{"date":96,"type":94},"2025-09-20",{"date":98,"type":81},"2026-08-02",{"name":5,"class":6},1]