[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100622167":3},{"organization":4,"armGroups":7,"interventions":29,"overallOfficials":10,"centralContacts":46,"locations":52,"responsibleParty":71,"collaborators":10,"id":75,"slug":76,"hasResults":77,"nctId":78,"briefTitle":79,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":82,"sex":83,"minAge":10,"maxAge":10,"enrollmentInfo":84,"targetDuration":10,"studyType":87,"phases":10,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":55,"whyStopped":10,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Universidad de Zaragoza","OTHER",[8,14,19,24],{"label":9,"type":10,"description":11,"interventionNames":12},"Experts Panel",null,"20 experts (3 women and 17 men) took part in the study. The expert panel consisted of 14 physiotherapists, 2 psychologists, and 3 physicians",[13],"Other: Iterative focus group sessions and individual evaluation phases",{"label":15,"type":10,"description":16,"interventionNames":17},"Dry Needling Patients","Patients who received a session of dry needling",[18],"Other: Dry Needling",{"label":20,"type":10,"description":21,"interventionNames":22},"Percutaneous Electrolysis Patients","Patients who received a session of percutaneous electrolysis",[23],"Other: Percutaneous Electrolysis",{"label":25,"type":10,"description":26,"interventionNames":27},"Percutaneous Neuromodulation Patients","Patients who received a session of percutaneous neuromodulation",[28],"Other: Percutaneous Neuromodulation",[30,34,38,42],{"type":6,"name":31,"description":32,"armGroupLabels":33,"otherNames":10},"Iterative focus group sessions and individual evaluation phases","The expert panel conducted iterative focus group sessions and successive individual evaluation phases until consensus was reached on the development of the acceptability scale.",[9],{"type":6,"name":35,"description":36,"armGroupLabels":37,"otherNames":10},"Dry Needling","One session of dry needling",[15],{"type":6,"name":39,"description":40,"armGroupLabels":41,"otherNames":10},"Percutaneous Electrolysis","One session of percutaneous electrolysis",[20],{"type":6,"name":43,"description":44,"armGroupLabels":45,"otherNames":10},"Percutaneous Neuromodulation","One session of percutaneous neuromodulation",[25],[47],{"name":48,"role":49,"phone":50,"phoneExt":10,"email":51},"Alberto Carcasona","CONTACT","+34666387648","acarcasona@unizar.es",[53],{"facility":54,"status":55,"city":56,"state":56,"zip":57,"country":58,"countryCode":59,"cosmosGeoPoint":60,"geoPoint":65,"contacts":66},"University of Zaragoza","RECRUITING","Zaragoza","50009","Spain","ES",{"type":61,"coordinates":62},"Point",[63,64],-0.87734,41.65606,{"lat":64,"lon":63},[67],{"name":68,"role":49,"phone":69,"phoneExt":10,"email":70},"Instituto de Investigación Sanitaria de Aragón","+34976716818","info@iisaragon.es",{"type":72,"investigatorFullName":73,"investigatorTitle":74,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Alberto Carcasona Otal","Principal Investigator","100622167","development-of-a-qualitative-scale-to-asses-the-acceptability-of-percutaneous-techniques-a-delphi-study-100622167",false,"NCT07380100","Development of a Qualitative Scale to Asses the Acceptability of Percutaneous Techniques. A Delphi Study","Accept_scale","Experts were required to:\n\n* have at least five years of experience in percutaneous techniques\n* have clinical experience working with patients with pain",true,"ALL",{"count":85,"type":86},65,"ESTIMATED","OBSERVATIONAL","This study aims to develop a new evaluation tool to assess patient acceptability of percutaneous interventions. A Delphi methodology will be implemented, involving the recruitment of a panel of experts in percutaneous interventions and pain management. The scale will be developed through several iterative phases until a final version is reached, comprising clearly defined domains, subdomains, items, and questions to be answered by patients in order to obtain an overall acceptability score for the percutaneous technique received. The scale is intended to be applicable across a wide range of percutaneous interventions and, consequently, to a broad patient population undergoing different percutaneous treatments depending on their clinical condition.",[90],"Acceptability of Percutaneous Interventions",[92,93,94],"Acceptability","Scale","Percutaneous Interventions","2026-06-09",{"date":97,"type":98},"2026-06-11","ACTUAL",{"date":100,"type":98},"2025-04-01",{"date":102,"type":86},"2026-08-01",{"name":5,"class":6},1]