[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100652424":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":34,"responsibleParty":73,"collaborators":76,"id":81,"slug":82,"hasResults":83,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":12,"eligibilityCriteria":87,"healthyVolunteers":83,"sex":88,"minAge":89,"maxAge":90,"enrollmentInfo":91,"targetDuration":12,"studyType":94,"phases":95,"briefSummary":97,"conditions":98,"keywords":100,"overallStatus":108,"whyStopped":12,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":118},{"fullName":5,"class":6},"Sanliurfa Education and Research Hospital","OTHER_GOV",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","NO_INTERVENTION","Participants in the control group will receive the standard verbal explanation and the institution-approved written informed consent form for the planned interventional pain procedure. No additional educational material will be provided.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Intervention Group","EXPERIMENTAL","Participants in the intervention group will receive the standard verbal explanation and the institution-approved written informed consent form for the planned interventional pain procedure, plus an ethics committee-approved simplified and visually supported procedure-specific information card.",[18],"Behavioral: Simplified and Visually Supported Procedure-Specific Information Card",[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":12},"BEHAVIORAL","Simplified and Visually Supported Procedure-Specific Information Card","An ethics committee-approved simplified and visually supported information card specific to the planned interventional pain procedure. This card uses plain language and schematic illustrations to highlight key aspects such as procedure purpose, steps, and potential risks. It is provided to participants in the intervention group as an educational supplement in addition to the standard informed consent process",[14],[26],{"name":27,"affiliation":5,"role":28},"Yağmur Can Dadakçı","PRINCIPAL_INVESTIGATOR",[30],{"name":27,"role":31,"phone":32,"phoneExt":12,"email":33},"CONTACT","+905333599730","yagmurcand@gmail.com",[35,51,62],{"facility":36,"status":12,"city":37,"state":37,"zip":38,"country":39,"countryCode":12,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"Ankara Bilkent City Hospital","Ankara","06800","Turkey (Türkiye)",{"type":41,"coordinates":42},"Point",[43,44],32.85427,39.91987,{"lat":44,"lon":43},[47],{"name":48,"role":31,"phone":49,"phoneExt":12,"email":50},"erkan yavuz akcaboy, prof. dr.","+905054514664","akcaboyyavuz@gmail.com",{"facility":5,"status":12,"city":52,"state":53,"zip":54,"country":39,"countryCode":12,"cosmosGeoPoint":55,"geoPoint":59,"contacts":60},"Sanliurfa","Şanlıurfa","63200",{"type":41,"coordinates":56},[57,58],38.79392,37.16708,{"lat":58,"lon":57},[61],{"name":27,"role":31,"phone":32,"phoneExt":12,"email":33},{"facility":63,"status":12,"city":52,"state":53,"zip":64,"country":39,"countryCode":12,"cosmosGeoPoint":65,"geoPoint":67,"contacts":68},"Sanliurfa Mehmet Akif Inan Education and Research Hospital","63300",{"type":41,"coordinates":66},[57,58],{"lat":58,"lon":57},[69],{"name":70,"role":31,"phone":71,"phoneExt":12,"email":72},"ahmet cemal kaya","+905393458515","ahmetcemal.kaya@saglik.gov.tr",{"type":28,"investigatorFullName":74,"investigatorTitle":75,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"Yağmur Can DADAKÇI","Principal Investigator",[77,80],{"name":78,"class":79},"T.C. Sağlık Bakanlığı Ankara Bilkent Şehir Hastanesi","OTHER",{"name":63,"class":79},"100652424","patient-understanding-of-informed-consent-in-interventional-pain-procedures-100652424",false,"NCT07772843","Patient Understanding of Informed Consent in Interventional Pain Procedures","Evaluation of Patient Understanding of Informed Consent Before Interventional Pain Procedures: A Multicenter Randomized Controlled Study","Inclusion Criteria:\n\n* Adults aged 18 to 85 years.\n* Patients scheduled to undergo an eligible interventional pain procedure included in the approved study protocol.\n* Ability to read, understand, and communicate in Turkish.\n* Ability to understand the study information and provide written informed consent for participation.\n* Willingness to participate in the study.\n\nExclusion Criteria:\n\n* Age below 18 years or above 85 years.\n* Severe cognitive impairment, mental incapacity, or any condition that prevents reliable understanding of the consent information or completion of the teach-back assessment.\n* Severe hearing or visual impairment that prevents the participant from receiving or understanding the study information, unless adequately corrected.\n* Active psychiatric illness or acute psychiatric episode that may affect comprehension, communication, or voluntary consent.\n* Emergency clinical condition requiring immediate intervention.\n* Inability or unwillingness to complete the teach-back assessment.\n* Inability or unwillingness to provide written informed consent for participation.","ALL","18 Years","85 Years",{"count":92,"type":93},360,"ESTIMATED","INTERVENTIONAL",[96],"NA","This multicenter randomized controlled study will evaluate whether simplified and visually supported procedure-specific information cards improve patients' understanding of informed consent before selected interventional pain procedures. Adult patients scheduled for an eligible procedure will be randomly assigned in a 1:1 ratio to either a control group or an intervention group. All participants will receive the routine verbal explanation and the standard institution-approved informed consent form for the planned procedure. Participants in the intervention group will additionally receive an ethics committee-approved simplified and visually supported information card related to the planned procedure. Participants in the control group will not receive the additional information card. After the information and consent process, patient understanding will be assessed using a standardized teach-back form before the clinical procedure. The study will compare understanding between the two groups.",[99],"Patient Understanding of Informed Consent Before Interventional Pain Procedures",[101,102,103,104,105,106,107],"Informed Consent","Patient Understanding","Teach-Back","Interventional Pain Procedures","Patient Education","Simplified Information Materials","Visual Information Materials","NOT_YET_RECRUITING","2026-08-14",{"date":111,"type":112},"2026-08-19","ACTUAL",{"date":114,"type":93},"2026-08-17",{"date":116,"type":93},"2026-12",{"name":5,"class":6},3]