[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"caregiving-stress\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:caregiving-stress":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,55,84,106],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100616423","integrative-therapeutic-programme-to-regulate-expressed-emotions-among-informal-caregivers-of-people-with-dementia-100616423",false,"NCT07305415","Integrative Therapeutic Programme to Regulate Expressed Emotions Among Informal Caregivers of People With Dementia","Integrative Therapeutic Programme to Regulate Expressed Emotions Among Informal Caregivers of People With Dementia: a Pilot Randomized Controlled Trial","COPE","Inclusion Criteria:\n\n* (1) With a high level of EE as indicated by a cut-off score of 35 or above on the Family Attitude Scale (Chinese version; FAS-C)\n* (2) Provides care at least 4 hours per day\n* (3) Consent to participate\n* (4) No acute psychiatric illness\n\nExclusion Criteria:\n\n* (1) With a score below 35 on the Family Attitude Scale (Chinese version; FAS-C)\n* (2) Provides care no more than 4 hours per day\n* (3) Does not consent to participate\n* (4) With acute psychiatric illness.","ALL","18 Years","100 Years",{"count":21,"type":22},56,"ESTIMATED","INTERVENTIONAL",[25],"NA","The dual-modal (face-to-face and online approaches), client-customized Caregivers Of dementia Processing Emotions (COPE) programme aims to\n\n1. reduce caregivers' Expressed Emotion (EE),\n2. reduce caregivers' depressive symptoms,\n3. reduce the behaviourally interactive social dynamic of maladaptation (i.e., dysfunctional dyadic relationship and quality of care), and\n4. improve caregivers' perceived stress from PwD's Behavioral and Psychological Symptoms of Dementia (BPSD).\n\nResearchers will compare COPE to a control group (standard therapy) to examine how effective the COPE programme is.\n\nParticipants will take part in:\n\nPretest prior to COPE implementation Post-test after COPE completion Follow up test in 3 months after COPE completion",[28,29,30,31],"BPSD (Behavioral and Psycological Symptoms of Dementia)","Expressed Emotion","Depressive Symptom","Caregiving Stress",[33,34,29,35,36,37,38,39,40,41],"BPSD","behavioral and psychological symptoms of dementia","Dementia caregivers","Dementia caregiving","preceived stress","caregiver depression","caregiving stress","caregiving relationship","dyadic care relationship","RECRUITING","2026-03-25",{"date":45,"type":46},"2026-03-31","ACTUAL",{"date":48,"type":46},"2025-12-20",{"date":50,"type":22},"2027-03-30",{"name":52,"class":53},"The University of Hong Kong","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":4,"briefSummary":65,"conditions":66,"keywords":69,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":54},"100546920","investigating-dyadic-expectations-about-arf-survivorship-ideas-100546920","NCT06401239","Investigating Dyadic Expectations About ARF Survivorship (IDEAS)","IDEAS","Patient Inclusion Criteria:\n\n* ≥18 years old\n* Meets study definition of ARF:\n\n  * The study defines ARF as meeting 1 of the following 3:\n\n    1. Mechanical ventilation via an endotracheal tube ≥24 consecutive hours OR\n    2. Non-invasive ventilation (CPAP, BiPAP) ≥24 consecutive hours that is not for obstructive sleep apnea or other stable use OR\n    3. High flow nasal cannula with fraction of inspired oxygen (FIO2)≥.5 and flow rate ≥ litres per minute (LPM) for ≥24 consecutive hours.\n  * Occasional rest periods of ≤1 hour are not deducted from the calculation of consecutive hours. Patients who are intubated for mental status or airway obstruction are not eligible unless they have simultaneous ARF.\n* Survival to hospital discharge to home\n* Speaks or reads English or Spanish\n* Identifies an adult who is expected to act as a primary care partner for at least the next 6 months.\n\nPatient Exclusion Criteria:\n\n* Pre-existing cognitive impairment (IQ-CODE \\>3.6)\n* Residing in a medical institution at hospital discharge\n* Receiving hospice care or life expectancy \\\u003C6 months\n* Homelessness or recent history of psychosis\n\nCare Partner Inclusion Criteria:\n\n* ≥18 years old\n* Speaks or reads English or Spanish\n\nCare Partner Exclusion Criteria:\n\n* Pre-existing cognitive impairment (IQ-CODE \\>3.6)",{"count":63,"type":22},235,"OBSERVATIONAL","The purpose of this observational study is to understand how adults who survive acute respiratory failure (ARF) and the people (usually family) who support ARF survivors after returning home think about the first 6 months of recovery. The study aims to find out if expectations about the recovery process after ARF are associated with mental health symptoms in both survivors and the survivor's care partners. Study participants will complete 3 surveys over 6 months. These surveys ask questions about participants' future expectations, feelings, and mood. Surveys can be completed online, over the phone, or on paper.",[67,31,68],"Acute Respiratory Failure","Mental Health Issue",[70,71,72,73,74],"ARF survivor","Caregiver","ICU recovery","Dyadic coping","Dyadic self-efficacy","2026-02-03",{"date":77,"type":46},"2026-02-05",{"date":79,"type":46},"2024-07-23",{"date":81,"type":22},"2027-07",{"name":83,"class":53},"Johns Hopkins University",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":23,"phases":93,"briefSummary":94,"conditions":95,"keywords":4,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100583783","closed-loop-and-neuroplasticity-based-mindfulness-program-for-family-caregivers-100583783","NCT06880822","Closed-Loop and Neuroplasticity-Based Mindfulness Program for Family Caregivers","Effects of a Closed-Loop and Neuroplasticity-Based Mindfulness Program for Reducing Stress in Family Caregivers of People with Dementia: a Randomized Controlled Trial with a Process Evaluation","Inclusion Criteria:\n\n* Age 18 or above;\n* Family caregiver of an individual who has been living in the community with a confirmed medical diagnosis of any type of dementia (verified through NGO records or care recipient's medical records) for more than one year;\n* Living in the same household as the care recipient;\n* Providing care with daily contact of 4 hours or more.\n\nExclusion Criteria:\n\n* Has participated in any structured mind-body intervention or structured psychosocial intervention within 6 months prior to recruitment;\n* Has an acute psychiatric condition that is potentially life-threatening or would limit participation in the study (indicated by answering \"yes\" to any of the six questions on the Columbia Suicide Severity Rating Scale).",{"count":92,"type":22},189,[25],"The aim of this study is to evaluate the effectiveness of a closed-loop and neuroplasticity-based mindfulness program for reducing stress among family caregivers of people with dementia. Participants will be randomly assigned to one of three groups: the closed-loop and neuroplasticity-based mindfulness program, a traditional mindfulness program, or brief education on dementia care. The closed-loop and neuroplasticity-based mindfulness program will include three weekly face-to-face training sessions (90 minutes each) and daily guided self-practice over 8 weeks via a mobile application. The traditional mindfulness program will not include the closed-loop approach but will feature general mindfulness practices with the same group size, duration, and frequency as the closed-loop program. The family caregivers in the control group will receive self-directed e-learning on dementia care with support from a registered nurse experienced in dementia care or elderly care, maintaining the same group size, duration, and frequency as the intervention groups. Evaluations will be conducted at baseline (0 weeks), immediately post-intervention (8 weeks), and during a follow-up assessment (6 months). All groups will complete the same assessments at the same time points.",[31],"NOT_YET_RECRUITING","2025-03-18",{"date":99,"type":46},"2025-03-20",{"date":101,"type":22},"2025-04-01",{"date":103,"type":22},"2027-04",{"name":105,"class":53},"The Hong Kong Polytechnic University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":113,"targetDuration":4,"studyType":23,"phases":115,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":4},"100563728","mindfulness-based-intervention-using-consumer-grade-wearable-devices-with-biofeedback-for-family-caregivers-of-people-with-dementia-100563728","NCT06619938","Mindfulness-Based Intervention Using Consumer-Grade Wearable Devices with Biofeedback for Family Caregivers of People with Dementia","Effects of Using a Consumer-Grade Wearable Device with Biofeedback and Brief Mindfulness Training for Stress Reduction in Family Caregivers of People with Dementia: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Family caregivers of an individual who has been residing in the community with a confirmed medical diagnosis of any type of dementia (from NGO record or the care-recipients\\' medical record);\n* Providing care for at least 4 hours or more per week;\n* Able to speak Cantonese (for understanding all teaching materials and instructions).\n\nExclusion Criteria:\n\n* Practicing or having recently learned meditation, mindfulness activities, and\u002For relaxation training in the last 6 months;\n* Regularly using wearable devices;\n* Diagnosed with a mental disorder such as bipolar disorder, schizophrenia, dementia, or depression in an acute phase.",{"count":114,"type":22},260,[25],"The aim of this study is to investigate the effectiveness of a brief mindfulness training intervention using a consumer-grade wearable device with biofeedback for reducing stress and promoting psychological health in family caregivers of people with dementia.\n\nThe intervention includes two weekly sessions, each lasting 90 minutes, of brief mindfulness training. The intervention group will be provided with a wearable device that offers biofeedback, which aims to promote their mindfulness practice and help the caregivers cultivate a mindful attitude in their daily activities, leading to stress reduction. Participants in the intervention group will attend a 30-minute briefing session to learn how to use the wearable device and understand the parameters displayed on the device. The caregivers will be instructed to practice mindfulness for 30 minutes every day over the course of eight weeks.\n\nParticipants will be randomly assigned to receive either the mindfulness intervention combined with biofeedback or the mindfulness intervention alone. Evaluations will be conducted at three time-points: baseline (0 weeks), mid-intervention (4 weeks), and post-intervention (8 weeks). Both groups will complete the same assessments at each time-point.",[31],"2024-09-28",{"date":120,"type":46},"2024-10-01",{"date":122,"type":22},"2024-10",{"date":124,"type":22},"2026-10",{"name":105,"class":53}]