[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"positive-mental-health\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:positive-mental-health":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100640408","family-finger-lifestyle-intervention-among-older-caregivers-100640408",false,"NCT07627386","Family FINGER: Lifestyle Intervention Among Older Caregivers","Family FINGER: a Pilot Randomised Controlled Trial of Healthy Lifestyle Intervention Versus Standard Care Among Older Caregivers","Inclusion Criteria:\n\n* Aged 65 and older.\n* Caregiver for a spouse with cognitive impairment.\n* Live in the same household with the care recipient.\n* The presence of modifiable risk factors for health: at least one self-reported lifestyle-related risk factor, or self-reported CAIDE dementia risk scores of 6 or higher, or a self-reported burdensome caregiving situation.\n\nExclusion Criteria:\n\n* A medication for Alzheimer's disease or diagnosis of dementia or suspected dementia (such as referral to or ongoing assessment process at memory clinic, or MoCa \\\u003C 18 points).\n* Any health condition affecting safe engagement in the intervention, or the caregiving situation is such that specialised social or health care services are needed before safe engagement in the intervention can be ensured, according to clinical judgement.",true,"ALL","65 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","The Family FINGER study enrolls caregivers aged 65 or older who live with and care for a spouse with cognitive impairment in North Savo, Finland (estimated n=100). This intervention builds on the FINGER study, which showed improved cognitive performance and health benefits, including better health-related quality of life. The intervention will be tailored to meet caregivers' specific needs.\n\nThe overall aim of the Family FINGER trial is to assess the efficacy of this intervention on the positive mental health of spousal caregivers.\n\nSpecific research questions are as follows:\n\n1. What is the efficacy of the Family FINGER intervention on mental health?\n2. What is the efficacy of the Family FINGER intervention on secondary outcome measures: dementia risk, cognition, and lifestyles?",[27],"Positive Mental Health",[29,30,31,32,33],"family care","caregiver","lifestyle intervention","positive mental health","older adults","NOT_YET_RECRUITING","2026-05-29",{"date":37,"type":38},"2026-06-04","ACTUAL",{"date":40,"type":21},"2026-05-28",{"date":42,"type":21},"2028-04-30",{"name":44,"class":45},"Tarja Välimäki","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":64,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":46},"100640320","tiva-mobile-health-intervention-for-family-caregivers-100640320","NCT07616284","TIVA Mobile Health Intervention for Family Caregivers","A Mobile Health Intervention for the Promotion of Mental Health in Family Caregivers: Protocol for a Pilot Study","TIVA-Pilot","Inclusion Criteria:\n\n* Adults aged 18 years or older.\n* Unpaid family caregivers of a person with chronic illness, disability, or dependency.\n* Providing regular caregiving assistance for at least 4 months.\n* Living in Portugal.\n* Ability to read and understand Portuguese.\n* Ownership and use of a smartphone with internet access compatible with the TIVA mobile application.\n* Willingness to install and use the TIVA app for 4 weeks.\n* Ability to provide informed consent.\n\nExclusion Criteria:\n\n* Severe cognitive impairment.\n* difficulties preventing independent use of the application or completion of study assessments.\n* Severe psychiatric disorder or acute mental health crisis interfering with participation.\n* Participation in another structured caregiver support or psychological intervention during the study period.\n* Inability to use a smartphone independently.","18 Years",{"count":57,"type":21},80,[24],"This pilot study aims to evaluate the feasibility, usability, and preliminary effects of the TIVA mobile health intervention in promoting positive mental health among family caregivers of older adults. TIVA is a culturally adapted mobile application based on Lluch's Positive Mental Health model and designed to support caregivers through daily activities, motivational messages, relaxation strategies, and psychoeducational content over a four-week intervention period.\n\nA pilot randomized controlled study with parallel allocation will be conducted involving family caregivers recruited in community and primary healthcare settings in Portugal. Participants will be allocated either to the TIVA intervention group or to a usual care control group. Outcomes will include positive mental health, caregiver burden, usability, satisfaction, adherence, and acceptability. Data will be collected at baseline, post-intervention, and follow-up.\n\nThis study intends to contribute to the development of accessible digital mental health strategies to support family caregivers and promote healthy ageing.",[27,61,62,63],"Family Caregivers","Mental Health Promotion","Caregiver Burden",[65,61,27,66,62,67,63],"TIVA mHealth","Older Adults","Mobile Application",{"date":69,"type":38},"2026-06-01",{"date":71,"type":21},"2026-09",{"date":73,"type":21},"2027-04",{"name":75,"class":45},"Universidade do Porto",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":83,"enrollmentInfo":84,"targetDuration":4,"studyType":22,"phases":86,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":46},"100634009","preliminary-efficacy-of-the-adoptmindful2careweb-a-web-based-mindful-parenting-post-adoption-intervention-for-adoptive-parents-100634009","NCT07534111","Preliminary Efficacy of the AdoptMindful2Care@Web: A Web-Based Mindful Parenting Post-Adoption Intervention for Adoptive Parents","Adopting eMental Health IV: A Randomized Controlled Pilot Trial to Evaluate a Web-Based Mindful Parenting Post-Adoption Intervention","Inclusion Criteria:\n\n* Have at least one adoptive child aged under 18 years\n* Have an adoption decreed by the court less than 24 months ago\n* Have no other adoption process in progress\n* Have reading and writing abilities in the Portuguese language\n* Have regular access to the internet and electronic devices\n\nExclusion Criteria:\n\n* Presence of a severe mental disorder (e.g., schizophrenia, substance abuse, bipolar disorder).\n* Have previously participated in the face-to-face, group-based version of the programme (pAdoptMindful2Care)","99 Years",{"count":85,"type":21},90,[24],"The development of post-adoption interventions aimed at promoting parental well-being and positive parenting is an urgent need. Mindful Parenting-based interventions appear to be particularly promising in this field, as they address parents' needs in coping with the emotional challenges of parenting and seem to foster greater compassionate, non-judgmental acceptance toward themselves and their children, as well as enhance the self-regulation of immediate emotional states in favor of long-term goals that support the parent-child relationship. However, the delivery of such interventions in face-to-face formats for adoptive parents (APs), particularly within the scope of universal prevention, faces considerable barriers (e.g., wide geographical dispersion of APs, limited mental health specialization among adoption service teams). eHealth tools represent an innovative pathway for intervention that may help overcome these barriers, given their multiple advantages, including: (1) improved access to healthcare regardless of time and location, (2) greater user autonomy in managing their own care, and (3) enhanced quality and innovation in service delivery, supported by the diversity, efficiency, and technological advancement of these systems. The primary goal of this study is to evaluate the effectiveness of AdoptMindful2Care@Web, a new 9-module, web-based post-adoption psychological intervention grounded in the principles of mindful parenting.\n\nThis pilot randomized controlled trial, with a two-arm design, precedes the full RCT planned as AdoptMindful2Care@Web. It is open to mothers and fathers who have at least one adoptive child under 18 years of age, whose adoption was legally decreed by the court less than 24 months prior to enrollment, who are not involved in any other ongoing adoption process, who are able to read and write in Portuguese, and who have regular access to the internet and electronic devices. A minimum of 90 families will be recruited with the support of all Portuguese governmental adoption agencies. After expressing interest in participating through an expression-of-interest form available on the project website, a member of the research team will contact them by telephone to conduct an initial screening (brief interview), with the following aims: (1) to clarify any questions regarding the study and (2) to assess their eligibility for participation (i.e., to confirm whether they meet the inclusion criteria and do not fall under any exclusion criteria). At the end of the telephone screening, they will be informed of the decision of eligibility. If deemed eligible and willing to participate, a specific date and time will be scheduled for completion of the online study assessment protocol corresponding to the first assessment point (T0). To support adherence to this appointment, a reminder will be sent on the scheduled day (via text message or email, as applicable).\n\nEligible participants will be randomly assigned to either the intervention group (AdoptMindful2Care@Web) or a waitlist control group (participants will receive the intervention after the study concludes). The intervention includes eight core modules plus a follow-up module, all carried out via an online platform, each lasting approximately 40 minutes. Participants in both groups will complete assessments at four time points: baseline, post-intervention, 1- and 2-month follow-up. These assessments will include both self-report (e.g., parenting stress) and hetero-report measures (e.g., children's emotional and developmental difficulties).",[89,27],"Parenting Stress",[89,27,91,92,93,94],"Mindful Parenting Intervention","Adoptive Parents","Post-Adoption","Web-Based","2026-04-16",{"date":97,"type":38},"2026-04-21",{"date":99,"type":21},"2026-04",{"date":101,"type":21},"2028-08",{"name":103,"class":45},"University of Coimbra"]