[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100620814":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":22,"locations":28,"responsibleParty":48,"collaborators":51,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":56,"sex":62,"minAge":63,"maxAge":64,"enrollmentInfo":65,"targetDuration":21,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":76,"overallStatus":31,"whyStopped":21,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"University of Amsterdam","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Imagery Rescripting","EXPERIMENTAL","The ImRs will follow the protocol as developed by Arntz and Weertman (1999), that was tailored for the primary care setting. The total of sessions will be set at 6. In session 1, the patient and therapist will create a list of core beliefs and memories to be rescripted. Session 1 will take place before the baseline phase, allowing us to assess core beliefs prior to the intervention. In session 2-6, one negative emotional memory is selected and rescripted (45 minutes per session). If necessary, a memory can be rescripted twice. In session 2-3 the therapist enters the image and rescripts the memory, whereas in session 4-6 the patient adult-self enters the image and rescripts the memory. If patients are uncomfortable doing so, session 4 can still be guided by the therapist.",[13],"Behavioral: Imagery Rescripting",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"BEHAVIORAL","During ImRs, the patient brings a negative memory to mind and changes, together with the therapist, the outcome of the memory into a more positive",[9],[20],"ImRs",null,[23],{"name":24,"role":25,"phone":26,"phoneExt":21,"email":27},"Lotte Stemerding","CONTACT","0031614401653","l.e.stemerding@uva.nl",[29],{"facility":30,"status":31,"city":32,"state":33,"zip":34,"country":35,"countryCode":36,"cosmosGeoPoint":37,"geoPoint":42,"contacts":43},"UvA Huisartsen","RECRUITING","Amsterdam","North Holland","1018VZ","Netherlands","NL",{"type":38,"coordinates":39},"Point",[40,41],4.88969,52.37403,{"lat":41,"lon":40},[44],{"name":45,"role":25,"phone":46,"phoneExt":21,"email":47},"Anna Kastelein","0031205252878","a.m.kastelein@uva.nl",{"type":49,"investigatorFullName":24,"investigatorTitle":50,"investigatorAffiliation":5,"oldNameTitle":21,"oldOrganization":21},"PRINCIPAL_INVESTIGATOR","Dr.",[52],{"name":30,"class":53},"UNKNOWN","100620814","imagery-rescripting-in-primary-care-100620814",false,"NCT07362511","Imagery Rescripting in Primary Care","Imagery Rescripting Within Primary Care to Manage Depression: A Single-Case Experimental Design","IMPACT MADE","Inclusion Criteria:\n\n* Main complaint of depressive feelings, as indicated by both the mental health assistant and the patient.\n* HADS score for the depression subscale ≥ 11.\n* Ability to understand, read, write and speak Dutch or English.\n* Age between 18 and 70.\n* Willingness to participate in the study and treatment.\n\nExclusion Criteria:\n\n* Acute suicide risk (BDI-II-item9 score of 3).\n* If the mental health assistant suspects that the patient may have a primary diagnosis of bipolar disorder, psychosis, substance use disorder, low IQ, or if the patient suffers from serious neurological problems such as dementia, then the patient is not included. There will not be a formal assessment of a primary diagnosis.","ALL","18 Years","70 Years",{"count":66,"type":67},12,"ESTIMATED","INTERVENTIONAL",[70],"NA","In the current study we aim to investigate the feasibility, acceptability, and effectiveness of ImRs offered by mental health assistants within primary care to reduce depressive symptoms. In a single-case experimental design (SCED) study, the following hypotheses will be tested:\n\n1. ImRs results in a reduction of depressive symptoms compared to baseline, and this reduction lasts up to six months.\n2. Patients with complaints of depressive symptoms find ImRs an acceptable form of intervention when offered by mental health assistants within a general practice setting.\n\nParticipants will wait for 2-4 weeks and then receive 5 sessions of ImRs over a period of 10 weeks. During these sessions, negative memories related to their depressed feelings are rescripted.",[73,74,75],"Major Depressive Diorder","Low Self-Esteem","Mood Disorders",[9,77,78],"Depression","Primary care","2026-01-14",{"date":81,"type":82},"2026-01-23","ACTUAL",{"date":84,"type":82},"2025-12-01",{"date":86,"type":67},"2027-01-31",{"name":5,"class":6},1]