[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"spouses\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:spouses":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100526465","phase-1-testing-a-peer-led-trauma-focused-intervention-for-significant-others-of-those-with-bpd-100526465",false,"NCT06135090","Testing a Peer-led Trauma-focused Intervention for Significant Others of Those With BPD","Development and Initial Testing of a Peer-Led Trauma-Focused Intervention for Significant Others of Individuals With Borderline Personality Disorder","Inclusion Criteria:\n\n* Self-identify as having experienced a trauma related to their loved one with BPD or related problems that impacts them\n* Has previously received the Family Connections program at Sashbear (i.e., a peer-led intervention that teaches family members skills for managing their relationships with their loved one with BPD and related problems)\n\nExclusion Criteria:\n\n* Engagement in suicidal or self-injurious behaviour in the past year\n* Elevated BPD symptoms","ALL","18 Years",{"count":19,"type":20},60,"ESTIMATED","INTERVENTIONAL",[23],"PHASE1","This project involves developing and piloting a peer-led intervention focused on posttraumatic stress symptoms for the family members and significant others of people with borderline personality disorder. The project involves collaborating with The Sashbear Foundation who will be delivering the trauma response program (TRP) that was developed by the investigative team to its network. In phase 1 of this project, the investigators will evaluate the first delivery of the TRP at The Sashbear Foundation and solicit feedback from peer-facilitators and recipients who consent to research participation. In phase 2 of this project, the investigators will evaluate the efficacy, acceptability, and safety of the delivery of the next two to four TRPs delivered at The Sashbear Foundation consisting of up to approximately 10 group members (maximum number of TRP recipient research participants in phase 2 is 40).",[26,27,28],"Posttraumatic Stress Disorder","Family Members","Spouses",[30,31,32,33,34],"Posttraumatic stress disorder","Borderline personality disorder","Peer-support","Family members","Significant others","NOT_YET_RECRUITING","2026-07-28",{"date":38,"type":39},"2026-07-29","ACTUAL",{"date":41,"type":20},"2026-10-01",{"date":43,"type":20},"2028-01-01",{"name":45,"class":46},"York University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100638969","construction-and-preliminary-evaluation-of-dyadic-acceptance-and-commitment-therapy-for-couples-with-fear-of-lung-cancer-recurrence-100638969","NCT07588347","Construction and Preliminary Evaluation of Dyadic Acceptance and Commitment Therapy for Couples With Fear of Lung Cancer Recurrence","Inclusion Criteria\n\nPatients:\n\n* Diagnosis of primary lung cancer confirmed by pathological examination.\n* Age ≥ 22 years for men and ≥ 20 years for women (legal marriage age in China).\n* Have undergone lung cancer surgery and are scheduled to receive the first round of radiotherapy and\u002For chemotherapy treatment\n* Fear of Cancer Recurrence Inventory-Short Form (FCRI-SF) score ≥ 13, indicating moderate-to-severe FCR.\n* Eastern Cooperative Oncology Group (ECOG) ≤2.\n* Aware of their diagnosis and willing to participate voluntarily.\n* Normal cognitive function (Montreal Cognitive Assessment \\[MoCA\\] score ≥ 26), alert and conscious, and able and willing to communicate their thoughts.\n\nSpouse Caregivers:\n\n* Identified by the patient as the primary caregiver, providing ≥ 50% of care in the past 2 weeks.\n* Legally married to the patient.\n* Age ≥ 22 years for men and ≥ 20 years for women.\n* Normal cognitive function (MoCA score ≥ 26), no diagnosed mental disorders, able to communicate effectively, and willing to share their thoughts.\n\nExclusion Criteria\n\nPatients:\n\n* Diagnosed mental disorders or currently receiving psychiatric treatment.\n* Presence of personality disorders, intellectual disability, memory disorders, brain injury, or neurological disease.\n* Concurrent malignant tumors in other organs.\n* Severe complications (e.g., chest pain and\u002For dyspnea due to pleural tumor invasion).\n* Spouse caregiver unwilling to participate.\n* History of upper limb fractures or surgery resulting in impaired hand function.\n* Participation in other similar psychological interventions.\n\nSpouse Caregivers:\n\n* Presence of serious comorbid conditions (e.g., respiratory failure, malignant tumors, or other critical illnesses).\n* Patient unwilling to participate.\n* Participation in other research studies.","20 Years",{"count":56,"type":20},72,[58],"NA","The goal of this clinical trial is to develop a simple, scientific, effective, and culturally adapted dyadic Acceptance and Commitment Therapy (ACT) intervention program (the ADAPT program) targeting fear of cancer recurrence (FCR) among lung cancer patients and their spouse caregivers. The study will also evaluate the feasibility, acceptability, and preliminary effectiveness of the ADAPT program.\n\nThe main research questions are as follows:\n\n* Is the ADAPT intervention program feasible and acceptable for lung cancer patients and their spouse caregivers?\n* Compared with usual care, can the ADAPT intervention program preliminarily reduce FCR levels in both patients and their spouse caregivers? Can the program improve coping styles, illness perceptions, family functioning, and intimate relationships among both patients and their spouse caregivers? Can the program enhance psychological flexibility and quality of life (QOL) in both patients and their spouse caregivers? Researchers will compare the ADAPT intervention program with usual care to evaluate its preliminary effectiveness in reducing FCR among lung cancer patients and their spouse caregivers.\n\nParticipants will:\n\n* Receive the ADAPT intervention twice during each radiotherapy and\u002For chemotherapy cycle, for a total of three treatment cycles (approximately 3 months);\n* Complete questionnaires at baseline (before the intervention), immediately after the intervention, and one month post-intervention;\n* Report outcomes including FCR severity, FCR triggers, psychological flexibility, illness perception, dyadic coping, family functioning, intimacy, and quality of life (QOL).",[61,62,28],"Lung Neoplasms","Acceptance and Commitment Therapy","2026-05-15",{"date":65,"type":39},"2026-05-19",{"date":63,"type":20},{"date":68,"type":20},"2027-06-30",{"name":70,"class":46},"Feifei Huang"]