[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100567602":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":36,"responsibleParty":81,"collaborators":84,"id":89,"slug":90,"hasResults":91,"nctId":92,"briefTitle":93,"officialTitle":94,"acronym":95,"eligibilityCriteria":96,"healthyVolunteers":91,"sex":97,"minAge":98,"maxAge":99,"enrollmentInfo":100,"targetDuration":30,"studyType":103,"phases":104,"briefSummary":106,"conditions":107,"keywords":109,"overallStatus":112,"whyStopped":30,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":122},{"fullName":5,"class":6},"University of Amsterdam","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Baseline-Preparation-Imagery Rescripting-Post Treatment","EXPERIMENTAL","Each participant follows this sequence: (1) 5-9 weeks waitlist during which no treatment is offered; (2) 4 weekly preparatory sessions. During these sessions the rationale of ImRs will be explained in more detail and a list of painful (childhood) memories to be addressed with ImRs is to be compiled, based on any further input from the patient; and a case conceptualization is made; (3) 12 sessions (45-60 minutes) of ImRs will be offered to participating patients. The ImRs treatment will be based upon the protocol described by Arntz \\& Weertman (1999). This protocol can be modified to tailor the needs of this study more specifically. (4) After end of active treatment (ImRs) 4 weeks follow during which only weekly assessments are done.",[13],"Behavioral: Imagery Rescripting",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Imagery Rescripting","Experimental: Baseline-Preparation-Imagery Rescripting-Post Treatment Each participant follows this sequence: (1) 5-9 weeks waitlist during which no treatment is offered; (2) 4 weekly preparatory sessions. During these sessions the rationale of ImRs will be explained in more detail and a list of painful (childhood) memories to be addressed with ImRs is to be compiled, based on any further input from the patient; and a case conceptualization is made; (3) 12 sessions (45-60 minutes) of ImRs will be offered to participating patients. The treatment for PAD will be based upon the protocol described by Arntz \\& Weertman (1999); (4) After end of active treatment (ImRs) 4 weeks follow during which only weekly assessments are done.",[9],[21],"ImRs",[23],{"name":24,"affiliation":5,"role":25},"Erica Pugliese, PhD","PRINCIPAL_INVESTIGATOR",[27,32],{"name":24,"role":28,"phone":29,"phoneExt":30,"email":31},"CONTACT","+31 (0)20 525 6810",null,"e.pugliese@uva.nl",{"name":33,"role":28,"phone":34,"phoneExt":30,"email":35},"Arnold van Emmerik, PhD","+31 (0)20 525 8604","a.a.p.vanemmerik@uva.nl",[37,54,71],{"facility":38,"status":30,"city":39,"state":40,"zip":41,"country":40,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Associazione Italiana Di Psicoterapia Cognitiva - Aipc","Bari","Italy","70125","IT",{"type":44,"coordinates":45},"Point",[46,47],16.86982,41.12066,{"lat":47,"lon":46},[50],{"name":51,"role":28,"phone":52,"phoneExt":30,"email":53},"Maria Grazia Foschino Barbaro, Psychology","+39 351 6208206","aipc.scuola@gmail.com",{"facility":55,"status":30,"city":56,"state":57,"zip":58,"country":59,"countryCode":60,"cosmosGeoPoint":61,"geoPoint":65,"contacts":66},"Sterk Huis","Amsterdam","Goirle","Rillaersebaan 75 5053 EA","Netherlands","NL",{"type":44,"coordinates":62},[63,64],4.88969,52.37403,{"lat":64,"lon":63},[67],{"name":68,"role":28,"phone":69,"phoneExt":30,"email":70},"Lenke Balogh","06-43828325","LenkeBalogh@sterkhuis.nl",{"facility":5,"status":30,"city":56,"state":30,"zip":30,"country":59,"countryCode":60,"cosmosGeoPoint":72,"geoPoint":74,"contacts":75},{"type":44,"coordinates":73},[63,64],{"lat":64,"lon":63},[76,79,80],{"name":77,"role":28,"phone":29,"phoneExt":30,"email":78},"Arnoud Arntz, Phd, Professor","A.R.Arntz@uva.nl",{"name":33,"role":28,"phone":29,"phoneExt":30,"email":35},{"name":24,"role":28,"phone":30,"phoneExt":30,"email":30},{"type":25,"investigatorFullName":82,"investigatorTitle":83,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"Erica Pugliese","Principal Investigator",[85,87],{"name":86,"class":6},"VU University of Amsterdam",{"name":88,"class":6},"Stichting Achmea Slachtoffer en Samenleving","100567602","imagery-rescripting-for-pathological-affective-dependence-and-intimate-partner-violence-100567602",false,"NCT06670326","Imagery Rescripting for Pathological Affective Dependence and Intimate Partner Violence","Imagery Rescripting As a Treatment for Pathological Affective Dependence: Helping Victims Break Free from Abusive Relationships","ImRs-PAD","Inclusion Criteria:\n\n* Experience of IPV (from a clinical interview)\n* Pathological Affective Dependence scale (PADS - Trait, State). As a prerequisite for PAD treatment and study participation, victims of IPV are required to establish a contact with the anti-violence center or shelters to receive co-assistance. The anti-violence center will take care of his\u002Fher physical safety and legal aspects.\n\nExclusion Criteria:\n\n* Comorbidity with the following diagnoses: psychosis, schizophrenia, bipolar disorder (conditions derived from a clinical interview or previous diagnostic reports), dissociative disorders (Dissociative Experience Scale, DES).\n* Organic brain disease\n* Intelligence Quotient (IQ) \\\u003C 80\n* High risk of self-harm or suicide\n* Current substance abuse severe level\n* Start of new medication within 2 months before beginning the study (medication used for longer periods can be continued; patients are requested to keep medication stable during the course of the study)\n* Having received ImRs (either as a stand-alone or embedded in a greater treatment such as cognitive behavior therapy (CBT) or schema therapy) within the last year\n* No other evidence-based treatment of MDD is allowed during the study.\n* Not able to plan enough time for weekly therapy sessions (45-60 minutes); weekly measurements (estimate of 5 minutes) and other measurements (estimate of 20 minutes); and the qualitative post-treatment interview (estimate of 60 minutes) during the study period.","FEMALE","18 Years","65 Years",{"count":101,"type":102},18,"ESTIMATED","INTERVENTIONAL",[105],"NA","The goal of this multiple baseline case series study is to evaluate the effectiveness of Imagery Rescripting for Pathological Affective Dependence (PAD) in victims of Intimate Partner Violence (IPV). The primary research questions are:\n\nDoes Imagery Rescripting reduce PAD and\u002For commitment to the abusive relationship after separation? Does Imagery Rescripting also reduce traumatic symptoms? Does Imagery Rescripting improve general mental health, self-compassion, and resilience in IPV victims? Participants will undergo a waiting period of 5-9 weeks (to assess time effects without treatment), followed by 4 weekly preparation sessions, 12 weekly Imagery Rescripting sessions, and 1 month of post-treatment.\n\nThroughout the study, participants will rate the severity of PAD and relational commitment on a weekly basis. They will also complete more detailed questionnaires assessing mental health, traumatic symptoms, resilience, and self-compassion before each phase, at 1 month post-treatment, 3 months post-treatment, and during follow-ups at 6 and 12 months.",[108],"Pathological Affective Dependence",[17,108,110,111],"Treatment","intimate partner violence","NOT_YET_RECRUITING","2024-10-30",{"date":115,"type":116},"2024-11-01","ACTUAL",{"date":118,"type":102},"2025-02-01",{"date":120,"type":102},"2026-02",{"name":5,"class":6},3]