[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100623499":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":35,"centralContacts":40,"locations":45,"responsibleParty":56,"collaborators":34,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":34,"eligibilityCriteria":64,"healthyVolunteers":60,"sex":65,"minAge":66,"maxAge":67,"enrollmentInfo":68,"targetDuration":34,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":48,"whyStopped":34,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"International Association Psychosomatics And Health Therapy","OTHER",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Active \"I-Reconstruction\" Therapy Group 1","EXPERIMENTAL","Participants randomized to the experimental group received the active psychotherapeutic intervention \"l-Reconstruction.\" This group consisted of adults with clinically significant anxiety who met all inclusion criteria of the study. Participants attended ten weekly online group therapy sessions led by a certified \"l-Reconstruction\" therapist. The group format was designed to facilitate therapeutic change through guided interpersonal interaction, normalization of experiences, and reflection within a structured therapeutic framework. All participants in the experimental group completed baseline, post-intervention, and follow-up assessments to evaluate changes in anxiety and related psychological outcomes.",[13],"Drug: Experimental: Active \"I-Reconstruction\" Therapy",{"label":15,"type":10,"description":11,"interventionNames":16},"Active \"I-Reconstruction\" Therapy Group 2",[13],{"label":18,"type":6,"description":19,"interventionNames":20},"Control Group","Standard Care (Treatment as Usual) Participants randomized to the control group received no therapeutic intervention during the study period. They continued with their usual daily activities and were not restricted from seeking any form of support or care outside the study. The control group participated only in scheduled psychological assessments at baseline, post-intervention, and follow-up time points, allowing for comparison of outcome trajectories between the intervention and non-intervention conditions.",[21],"Drug: Standard Care (Treatment as Usual)",[23,30],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"DRUG","Experimental: Active \"I-Reconstruction\" Therapy","The intervention consisted of a structured group psychotherapy program based on the \"l-Reconstruction\" method. The program included ten weekly group sessions, each lasting 120 minutes, delivered online by a certified therapist trained in the method. The intervention targeted anxiety through therapeutic work with preverbal trauma and internal conflicts by reconstructing core personality components related to desire, ownership, and the capacity for pleasure. The therapeutic process combined psychoeducation, analysis of preverbal acts, exploration of emotional and bodily responses, reconstruction of traumatic experiential patterns, and structured group reflection and integration. The intervention followed a standardized protocol to ensure consistency across groups and therapists.",[9,15],[29],"I-Reconstruction",{"type":24,"name":31,"description":32,"armGroupLabels":33,"otherNames":34},"Standard Care (Treatment as Usual)","Participants assigned to the control group did not receive any structured psychotherapeutic intervention as part of the study. During the intervention period, no active treatment, group sessions, or therapeutic procedures were provided by the research team. The control condition was designed to serve as a non-intervention comparison group for evaluating the effects of the \"l-Reconstruction\" group psychotherapy.",[18],null,[36],{"name":37,"affiliation":38,"role":39},"Tetiana Pavlenko","International Association of Psychosomatics and Health Therapy","PRINCIPAL_INVESTIGATOR",[41],{"name":37,"role":42,"phone":43,"phoneExt":34,"email":44},"CONTACT","+380976953203","tanjapavlenko28223@gmail.com",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":34,"geoPoint":34,"contacts":54},"International Association of Psychosomatics and Body Therapy","RECRUITING","Kyiv","Kyiv Oblast","03057","Ukraine","UA",[55],{"name":37,"role":42,"phone":43,"phoneExt":34,"email":44},{"type":39,"investigatorFullName":37,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":34,"oldOrganization":34},"Research Director, author of the \"I - reconstruction\" method, Supervisor","100623499","group-therapy-using-the-i-reconstruction-psychotherapy-method-to-reduce-anxiety-levels-100623499",false,"NCT07397429","Group Therapy Using the \"I-Reconstruction\" Psychotherapy Method to Reduce Anxiety Levels","Group Therapy Using the I-Reconstruction Psychotherapy Method for Reducing Anxiety Levels: a Randomized Controlled Trial","Inclusion Criteria:\n\nAge between 18 and 55 years (inclusive).\n\nClinically significant level of anxiety according to the Beck Anxiety Inventory (BAI) ≥ 9 points.\n\nAnxiety subscale score on the Hospital Anxiety and Depression Scale (HADS-A) ≥ 11 points.\n\nSignificant level of preverbal trauma according to the \"Diagnostics of Preverbal Dysregulation\" (DPD, T. Pavlenko) questionnaire: total score ≥ 16.\n\nSpecific subscale scores in DPD: \"Desire\" ≥ 5, \"Satisfaction\" ≥ 5, and \"Possession\" (Obsession) ≥ 6 points.\n\nPresence of internal conflicts according to the \"Internal Conflict Test\" (ICT) ≥ 1 point on the skin tissue measurement scale.\n\nWillingness to comply with the study protocol and the online therapy format.\n\nExclusion Criteria:\n\nCurrent participation in any other psychotherapy during the study.\n\nUse of any psychotropic medications within the last 30 days (antidepressants, tranquilizers, neuroleptics, mood stabilizers).\n\nDiagnosed severe mental disorders (according to ICD-10\u002FDSM-5) requiring specialized psychiatric care or inpatient treatment.\n\nPresence of acute suicidal risk.\n\nSubstance abuse (alcoholism, drug addiction).\n\nFailure to meet any of the threshold values specified in the inclusion criteria.","ALL","18 Years","55 Years",{"count":69,"type":70},36,"ESTIMATED","INTERVENTIONAL",[73],"NA","Brief Summary of the Study The aim of this clinical trial is to find out if the group therapy method \"Self-Reconstruction\" helps to reduce anxiety in adults. The researchers want to see if the participants' emotional state becomes more stable after completing the course.\n\nThe main questions that this study aims to answer are:\n\nDo people's anxiety levels decrease after taking the course of \"I-Reconstruction\" classes?\n\nDo the positive effects of the classes persist 3, 6 and 12 months after they finish?\n\nDo the participants' quality of life and ability to enjoy life improve?\n\nThe researchers will compare a group of people who attend the therapy classes with a group of people who receive usual care to see if the new method is more effective.\n\nParticipants will:\n\nParticipate in 10 online group meetings once a week.\n\nDo simple breathing and movement exercises to calm the body and emotions.\n\nDiscuss your feelings and desires with a professional in a safe group.\n\nComplete questionnaires about your condition at the beginning, during, and after the study.",[76,77],"Anxiety","Anxiety Depression",[79,80,81,82,83,84,85,86,87],"Anxiety,","Group Therapy","Randomized Controlled Trial - RCT","Anxiety Disorders","Psychotherapeutic Intervention","Depression","I - Reconstruction","Internal Conflict Test","Preverbal trauma","2026-02-04",{"date":90,"type":91},"2026-02-09","ACTUAL",{"date":93,"type":70},"2026-03-02",{"date":95,"type":70},"2027-06",{"name":5,"class":6},1]