[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"social-support\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:social-support":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,51,80,111,138,166,199,228,262],{"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":34,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100645009","empowerher-hybrid-digital-intervention-for-breast-cancer-survivors-100645009",false,"NCT07676591","EmpowerHer: Hybrid Digital Intervention for Breast Cancer Survivors","EmpowerHer: Protocol for a Multicentre Randomized Controlled Trial Evaluating a Hybrid Digital Exercise and Education Intervention for Breast Cancer Survivors Across Five European Countries","EmpowerHer","Inclusion Criteria:\n\n* Women aged 18-65 years.\n* History of breast cancer.\n* Completed primary treatment (surgery, chemotherapy, and\u002For radiotherapy; adjuvant hormone therapy is permitted).\n* No evidence of active or metastatic disease at enrolment.\n* Able to provide informed consent and communicate in the local language.\n* Own and are able to use a smartphone.\n* Willing to engage in the exercise program.\n\nExclusion Criteria:\n\n* Cognitive impairment preventing safe participation or questionnaire completion.\n* Uncontrolled medical conditions that contraindicate exercise (e.g., unstable cardiac disease).\n* Concurrently enrolled in another structured exercise or survivorship study.\n* Pregnant or breastfeeding.","FEMALE","18 Years","65 Years",{"count":21,"type":22},147,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn if a 12-week hybrid exercise and education program (EmpowerHer) works to improve health-related quality of life in breast cancer survivors aged 35 to 65.\n\nThe main questions it aims to answer are:\n\n* Does the EmpowerHer program improve the everyday quality of life of participants?\n* Does the program lower fatigue, anxiety, and depression while raising physical fitness?\n\nResearchers will compare the EmpowerHer program to usual medical care to see if the program works better to help survivors recover.\n\nParticipants will:\n\n* Use a mobile application at home at least twice a week for structured exercise.\n* Read short educational modules on the mobile application about health after cancer.\n* Attend weekly in-person motivational group sessions with a program facilitator.\n* Complete health and physical tests at the start, at 12 weeks, and 3 months later.",[28,29,30,31,32,33],"Breast Cancer","Cancer Survivors","Quality of Life","Exercise Therapy","Social Support","Mobile Applications",[35,31,36,33,32,37,30],"Breast Cancer Survivors","Digital Health","Multicentre Randomized Controlled Trial","NOT_YET_RECRUITING","2026-06-23",{"date":41,"type":42},"2026-06-30","ACTUAL",{"date":44,"type":22},"2027-07-01",{"date":46,"type":22},"2028-06-30",{"name":48,"class":49},"University of Valencia","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":57,"minAge":18,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":50},"100629196","activating-social-resources-in-psychotherapy-seeking-individuals-effectiveness-and-timing-of-a-social-support-just-in-time-adaptive-intervention-100629196","NCT07471529","Activating Social Resources in Psychotherapy-Seeking Individuals: Effectiveness and Timing of a Social Support Just-in-Time Adaptive Intervention","Inclusion Criteria:\n\n* indicating to seek outpatient psychotherapy\n* elevated levels of self-reported depressive symptoms (Beck Depression Inventory-II (BDI) score \\> 13 (out of 63); Kühner et al., 2007)\n* owning a smartphone\n* signing the informed consent form\n\nExclusion Criteria:\n\n* first session for outpatient psychotherapy is scheduled within four weeks\n* suicidal ideation (values \\> 2 in BDI item 9)\n* presence of manic symptoms (Mood Disorder Questionnaire (MDQ) score \\> 7), - shift work\n* age below 18 or above 70","ALL","70 Years",{"count":60,"type":22},120,[25],"This study evaluates a Just-In-Time Adaptive Intervention (JITAI) aiming to foster social support processes for adults with elevated depressive symptoms awaiting outpatient psychotherapy. Utilizing a daily-level micro-randomized trial (MRT) design conducted over 21 days, participants are assessed six times daily. Participants are randomized across four conditions: (1) vulnerability-triggered, (2) vulnerability and receptivity-triggered, (3) support-need-triggered, and (4) a no-intervention control. The primary objective of this study is to evaluate the effectiveness of the JITAI in reducing daily depressive symptoms and increasing received social support (primary outcomes), as well as reducing daily loneliness and enhancing perceived social support (secondary outcomes). Furthermore, the study aims to compare the relative efficacy of three distinct triggering strategies to identify the most effective timing for intervention delivery.",[64,32,65],"Loneliness","Depressive Symptoms",[32,64,67,68,69,65],"Just-in-Time Adaptive Intervention","JITAI","Ecological Momentary Intervention","RECRUITING","2026-04-29",{"date":73,"type":42},"2026-04-30",{"date":75,"type":42},"2026-04-22",{"date":77,"type":22},"2026-12",{"name":79,"class":49},"University of Zurich",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":57,"minAge":87,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":23,"phases":91,"briefSummary":92,"conditions":93,"keywords":97,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":4},"100633368","evaluating-whatsok-helpline-for-youth-with-concerns-about-sexual-thoughts-and-behaviors-100633368","NCT07525778","Evaluating WhatsOK Helpline for Youth With Concerns About Sexual Thoughts and Behaviors","A Randomized Control Trial Evaluation of WhatsOK for the Primary Prevention of Problematic Sexual Behaviors Among Youth","Inclusion Criteria:\n\n* must be ages 14-17 years at baseline\n* must have concerns about their sexual thoughts or behaviors\n* must be able to read, write, and speak in English\n\nExclusion Criteria:\n\n* Under 14 or over 17 years of age\n* Does not have concerns about their sexual thoughts or behaviors\n* Previously contacted a helpline or hotline for concerns about their sexual thoughts or behaviors\n* Is not able to read, write, or speak in English\n* Does not consent to participate","14 Years","17 Years",{"count":90,"type":22},920,[25],"Research suggests up to 77% of harmful sexual experiences during childhood are caused by other youth. Sometimes called peer-peer abuse or youth-perpetrated child sexual abuse, problematic and harmful sexual behavior among youth (PHSBY) involves sexual behaviors that are not developmentally appropriate and have potential to cause harm to the child or children involved.\n\nCompared to adults, children and adolescents who engage in sexual exploration are at greater risk of making mistakes or causing harm, in large part because they have insufficient information about healthy sexual behavior and development, consent, and related concepts. However, the available support, information, and resources for youth who have engaged in or are at risk of engaging in PSHB are limited.\n\nTo address these unmet needs, Stop it Now! (stopitnow.org) created the first youth-focused website and helpline services (WhatsOK) for young people with concerns about their sexual thoughts, interests, and behaviors. WhatsOK.org is a microsite developed specifically for youth aged 14-21 years. If a child or young person has concerns about their sexual thoughts or behaviors, the WhatsOK Online Help Center and Helpline can provide support and resources to support healthy behavior and prevent problematic or harmful behavior. If someone has already engaged in PHSBY or if they are unsure about whether what has been done is illegal, they can still reach out for confidential help to learn about taking steps to stop.\n\nPreliminary findings from a longitudinal, observational study of the WhatsOK helpline suggest that youth are willing to seek out help for their (and others') sexual interests and behaviors, highlighting the critical need for prevention strategies targeting youth with potentially concerning sexual behaviors. We examined the characteristics of contacts to the WhatsOK helpline via data collected from pre-set questions on age, primary reason for contact, timing of inquiry relative to other help-seeking, and timing relative to harm caused. Most inquiries came from youth aged 14 to 21 (57.7%) via email (54.4%). Over half (54.6%) had already engaged in harmful or illegal behaviors or were potentially at risk to do so. The majority of contacts sought help prior to seeking out other external professional resources (54%).\n\nThe current study is a randomized control trial evaluating the impact of the WhatsOK helpline in reducing PHSBY and improving help-seeking attitudes and behavior in a sample of participants ages 14-17 with concerns about their sexual thoughts and behaviors.",[94,32,95,96],"Mental Health","Perceived Self-efficacy","Sexual Behavior",[98,99,100,101],"youth sexual behavior","adolescents","support services","helpline","2026-04-07",{"date":104,"type":42},"2026-04-13",{"date":106,"type":22},"2026-04-06",{"date":108,"type":22},"2029-09-29",{"name":110,"class":49},"Center for Violence Prevention Research Inc",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":118,"sex":57,"minAge":119,"maxAge":87,"enrollmentInfo":120,"targetDuration":4,"studyType":23,"phases":122,"briefSummary":123,"conditions":124,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":5},"100488388","intervention-to-prevent-behavioral-health-symptoms-among-pandemic-affected-children-100488388","NCT05639465","Intervention to Prevent Behavioral Health Symptoms Among Pandemic Affected Children","Pragmatic RCT of a Multi-level Mechanistically Informed Community Intervention to Prevent the Onset of Behavioral Health Symptoms Among Socioeconomically Disadvantaged Pandemic Affected Children","Inclusion Criteria:\n\n* child experienced the COVID-19 pandemic and an additional large-scale disaster\n* child score is 5 or above on the Strengths and Difficulties Questionnaire\n* child is in 3- 8th grade at enrollment\n* the parent or guardian must complete informed consent and child assent\n* child must speak English or Spanish.\n\nExclusion Criteria:\n\n* child is currently receiving treatment for a diagnosed mental health condition\n* children who are not able to interact with other students in a group work format, regardless of IEP status",true,"8 Years",{"count":121,"type":22},800,[25],"Racial and ethnic minority children who live in socioeconomically disadvantaged communities are disproportionately impacted by pandemic and climate-induced disasters. Although effective interventions have been designed to treat mental health related symptoms in post-disaster settings, accessible, empirically supported prevention interventions are needed to prevent the onset of mental and behavioral health issues among these children. Building on our preliminary findings, the proposed study examines the efficacy and implementation of a COVID-19 adapted disaster focused prevention intervention, Journey of Hope-C19, in preventing behavioral health and interpersonal problems among racial and ethnic minority children who live in low-resource high poverty communities.",[125,126,127,128,32],"Emotional Distress","Prosocial Behavior","Pandemic, COVID-19","Coping Skills","2026-01-21",{"date":131,"type":42},"2026-01-23",{"date":133,"type":42},"2022-11-15",{"date":135,"type":22},"2027-05-15",{"name":137,"class":49},"University of Illinois at Urbana-Champaign",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":118,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":144,"targetDuration":4,"studyType":23,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":50},"100497921","understanding-the-role-of-doulas-in-supporting-people-with-pmads-100497921","NCT05763537","Understanding the Role of Doulas in Supporting People With PMADs","Inclusion Criteria:\n\n* Participants must be over the age of 18\n* Currently pregnant and between 13 and 26 gestational weeks at the time of enrollment\n* Live in a HRSA-designated rural area of Montana\n\nExclusion Criteria:\n\n* They are under the age of 18\n* Not currently pregnant\n* Not between 13-26 gestational weeks at the time of enrollment\n* If they do not live in a HRSA-designated rural are of Montana.",{"count":145,"type":22},75,[25],"Detailed Description The doula-led intervention developed during the first phase of this project will be pilot tested for feasibility. Following the recruitment procedures described in the recruitment and retention plan, approximately 75 participants will be enrolled into the study. Twenty-five of the participants will receive regular doula care and 25 of the participants will receive care from a doula trained in the PMAD doula training throughout their pregnancy, childbirth, and postpartum time period, following the intervention procedures developed in Aim 2 of this study. Twenty-five women will not receive care from a doula and will receive perinatal care as usual. Women in all groups will take surveys via REDCap during their enrollment in the intervention, at 1 month postpartum, 3 months, and 6 months postpartum (at the conclusion of the intervention). All participants who receive the PMAD doula intervention will complete checklists after each session with their doula, to assess fidelity to the intervention. Participant communication with their doula via patient notebook will also be assessed for fidelity to the intervention.",[149,150,151,152,32,94,153,154,155,156],"Maternal Health","Pregnancy","Delivery, Obstetric","Self Efficacy","Substance-Related Disorders","Postpartum Depression","Depression","Mental Health Services","2025-11-12",{"date":159,"type":42},"2025-11-14",{"date":161,"type":42},"2024-11-26",{"date":163,"type":22},"2026-07-31",{"name":165,"class":49},"University of Montana",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":172,"eligibilityCriteria":173,"healthyVolunteers":118,"sex":17,"minAge":174,"maxAge":4,"enrollmentInfo":175,"targetDuration":4,"studyType":23,"phases":177,"briefSummary":178,"conditions":179,"keywords":182,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":50},"100593809","economic-empowerment-and-health-promotion-of-uganda-grandmother-caregivers-100593809","NCT07011264","Economic Empowerment and Health Promotion of Uganda Grandmother-caregivers.","Development and Testing of BAJJAJJA: An Intervention to Promote Economic Empowerment and Health of Grandmothers Who Provide Primary Care for Grandchildren in Uganda","BAJJAJJA","Inclusion Criteria:\n\nParticipants must meet all of the following criteria:\n\n* Female, aged 50 years or older (reflecting the post-reproductive age range in Uganda)\n* Luganda-speaking (commonly spoken language).\n* Primary caregiver of at least one minor grandchild (under 18 years) for more than six months\n* Able to independently perform activities of daily living (e.g., cooking, bathing)\n\nExclusion Criteria:\n\nParticipants will be excluded if they:\n\n* Are cohabitating with their adult children\n* Are grandmothers under the age of 50","50 Years",{"count":176,"type":22},24,[25],"Background:\n\nThere are an estimated 163 million children worldwide who are under the care of their grandparents or other relatives. In Uganda, social determinants of health (i.e., poverty, wars, and maternal and perinatal conditions) threaten the middle generation (age 15-49) and leave older adults, especially grandmothers (Bajjajja), to become the safety net. Yet, in this region, knowledge about effective interventions that support the health and wellbeing of these GMCs is limited to nonexistent. As such, Dr. Matovu proposes to refine, adapt, and test her BAJJAJJA intervention that she developed.\n\nSpecific Aims:\n\nDr. Matovu will achieve this goal through three Specific Aims:\n\n1. Refine and adapt the BAJJAJJA intervention components through a collaborative and iterative feedback process with a diverse community group of 18 members;\n2. Test the feasibility, acceptability and preliminary efficacy of the BAJJAJJA intervention in improving economic and health outcomes among 24 Ugandan GMCs; and\n3. Explore the barriers and facilitators to (3a) maintenance of the BAJJAJJA individual intervention benefits and (3b) sustainability of the income generating activity at 6 months post-intervention.\n\nThis innovative study will utilize a community-engaged approach that emphasizes the meaningful involvement of community partners to develop an intervention that targets GMCs. Her outcomes will support her future efficacy clinical trial to test a novel multi-component and community-engaged BAJJAJJA intervention to promote the mental, physical, and economic wellbeing of GMCs.",[180,181,32],"Financial Burden","Health Behavior",[183,184,185,186,187,188,189],"NIH Stage Model","intervention testing","intervention development","physical challenges","mental challenges","financial stress","Ugandan grandmother-caregivers","2025-08-11",{"date":192,"type":42},"2025-08-14",{"date":194,"type":22},"2025-10-01",{"date":196,"type":22},"2029-08-30",{"name":198,"class":49},"University of Utah",{"id":200,"slug":201,"hasResults":11,"nctId":202,"briefTitle":203,"officialTitle":203,"acronym":204,"eligibilityCriteria":205,"healthyVolunteers":118,"sex":57,"minAge":18,"maxAge":4,"enrollmentInfo":206,"targetDuration":4,"studyType":23,"phases":208,"briefSummary":209,"conditions":210,"keywords":216,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":50},"100569172","preventt2-together-examining-the-efficacy-of-couple-based-lifestyle-intervention-to-prevent-type-2-diabetes-100569172","NCT06690788","PreventT2 Together: Examining the Efficacy of Couple-based Lifestyle Intervention to Prevent Type 2 Diabetes","PT2T","Inclusion Criteria:\n\n1. \"Target partner\" is eligible for the National DPP per CDC eligibility requirements:\n\n   * BMI ≥ 25 kg\u002Fm² (≥ 23 kg\u002Fm² if Asian American), and\n   * Do not have a diagnosis of type 1 or type 2 diabetes, and\n   * Not currently pregnant, and\n   * High risk for type 2 diabetes based on: (i) CDC Prediabetes Risk Test score ≥ 5, (ii) clinically diagnosed Gestational Diabetes during a previous pregnancy (for women), or (iii) a blood test result indicative of prediabetes in the past year (i.e., fasting blood glucose 100-125 mg\u002Fdl; plasma glucose 140-199 mg\u002Fdl measured 2 hours after a 75 g glucose load; or HbA1c 5.7%-6.4%).\n2. The couple has lived together for 1+ years.\n3. Both partners are willing to participate in the research.\n4. Both partners are at least 18 years old.\n5. Both partners are fluent in English.\n\nEXCLUSION CRITERIA:\n\n1. \"Supporting partner\" has a diagnosis of Type 2 Diabetes.\n2. Either partner:\n\n   * Has a diagnosis of another chronic disease (unless no major events\u002Fchanges for 3+ months), or\n   * Is currently on medication or engaged in lifestyle intervention for prediabetes or obesity, or\n   * Has previously participated in the National DPP, or\n   * Reports discomfort participating in a lifestyle program with their partner, or\n   * Reports a low level of relationship commitment (i.e., \"4\" or lower on a scale from 1 (do not agree at all) to 7 (agree completely) on the item \"I want this relationship to stay strong no matter what rough times we encounter.\"; Owen et al., 2011).",{"count":207,"type":22},324,[25],"Nearly half of adults in the United States have or are at risk of developing type 2 diabetes. The overall goal of this community-engaged research is to examine the efficacy of an innovative couple-based lifestyle intervention to prevent type 2 diabetes that is applicable to a broad range of partnered adults in the United States. By simultaneously targeting lifestyle and perceived support from romantic partners, there is a high likelihood of creating lasting changes in both",[211,212,213,32,214,215],"Prediabetic State","Life Style","Intervention Study","Physical Activity","Obesity",[217,218,32,219],"Lifestyle Intervention","Prevention","Couple Relationships","2025-05-28",{"date":222,"type":42},"2025-05-30",{"date":224,"type":42},"2025-03-06",{"date":226,"type":22},"2028-11",{"name":198,"class":49},{"id":229,"slug":230,"hasResults":11,"nctId":231,"briefTitle":232,"officialTitle":232,"acronym":233,"eligibilityCriteria":234,"healthyVolunteers":118,"sex":57,"minAge":18,"maxAge":235,"enrollmentInfo":236,"targetDuration":4,"studyType":23,"phases":238,"briefSummary":240,"conditions":241,"keywords":246,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":253,"lastUpdatePostDateStruct":254,"startDateStruct":256,"completionDateStruct":258,"leadSponsor":260,"locationsCount":50},"100587883","phase-2-cultural-adaptation-of-a-web-based-app-myplan-thailand-to-empower-and-support-friends-and-family-of-intimate-partner-violence-survivors-100587883","NCT06934174","Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends and Family of Intimate Partner Violence Survivors","IPV","Inclusion Criteria:\n\n* being female or males who have a female friend currently (past 6 months) experiencing IPV\n* Thai speaking\u002Freading\n* At least 18 years old\n* Have access to a safe smart-phone or computer with internet\n* Have safe email address\n* Living in Thailand\n\nExclusion Criteria:\n\n* Cannot speak\u002Freading Thai\n* Less than age 18 years old\n* Cannot access to a safe smartphone or computer with internet\n* Not living in Thailand","60 Years",{"count":237,"type":22},100,[239],"PHASE2","This research will support and empower friends\u002Ffamily (F\u002FF) of intimate partner violence (IPV) survivors in Thailand, where IPV is critical and common, and survivors first and foremost seek help for abuse from their F\u002FF. myPlan app (www.myPlanapp.org) is a free mobile evidence-based intervention app to prevent IPV. The app was first developed in the United States (US) and has been disseminated to high-income countries (e.g., New Zealand, Canada, Australia) and lowincome (Kenya). One new hope for improving survivors' psychological and well-being is adapting and introducing the myPlan app for the concerned friends\u002Ffamily who support survivors in Thailand.\n\nTherefore, the propose of this longitudinal research study, Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends\u002FFamily of Intimate Partner Violence Survivors in Thailand, will have two consecutive phases with three aims: 1) To tailor the myPlan app content for concerned F\u002FF members of Thai IPV survivors, 2) To integrate the adapted myPlan app content for concerned F\u002FF members of Thai IPV survivors, 3) To test the feasibility and acceptability of the adapted myPlan app with concerned F\u002FF members of Thai IPV survivors. Phase 1 (Year 1-2) will achieve aim 1-2 to tailor the myPlan app with Thai survivors and friends\u002Ffamily. The investigators will review current content and conduct in-depth interviews with survivors and concerned F\u002FF members on social norms associated with IPV, informal support systems and the role\u002Fresponsibility in helping survivors, safety strategies used by concerned F\u002FF members and negative consequences for both survivor and F\u002FF member providing support. Moreover, in phase 1, the adapted content will be pilot tested with concerned F\u002FF members of survivors by using cognitive techniques and theater-testing methodology.\n\nPhase 2 (Year 3-4) will achieve aim 3 to test the feasibility and acceptability of the adapted myPlan app with F\u002FF. The investigators will conduct a two-group RCT design with concerned F\u002FF member randomized to receive a) the myPlan app for F\u002FF member, or b) standard usual-care safety planning information. Primary outcomes for F\u002FF members include change in knowledge and attitudes towards IPV and F\u002FF empowerment to plan and take safety support survivor. Secondary outcomes will examine change in F\u002FF' distress, frustration and consequences for supporting the survivor. This phase will also collect feasibility and acceptability data to informed a planned R01 submission in Year 3 of the study. The K43 application outlines a four-year plan to support a candidate who is a nursing instructor with 15 years of work in diverse projects, settings, and disciplines; which positions her for a successful career as an independent researcher in research field of intimate partner violence. The career development plan provides a sequence of carefully selected training and mentoring experiences, including coursework to increase research capacity, leadership skills, mentored research leading to a R01 proposal, peer reviewed publications, and professional networking, that will catapult this research to the next level of research achievement. The team will be a collaboration between the Boromarajonani College of Nursing Khon Kaen (BCNKK), Khon Kaen One Stop Crisis Center (OSCC), Johns Hopkins University (JHU), Notre Dame of Maryland University (NDM), and Auckland University of Technology (AUT), New Zealand.",[242,32,243,244,245],"Intimate Partner Violence (IPV)","Empowerment","mHealth","Effectiveness",[247,248,249,250,251,252],"Intimate partner violence","Friends\u002FFamily memeber","Safety","Social support","mHealth intervention","Thailand","2025-05-08",{"date":255,"type":42},"2025-05-13",{"date":257,"type":42},"2025-04-17",{"date":259,"type":22},"2026-06",{"name":261,"class":49},"Boromarajonani College of Nursing, Khon Kaen",{"id":263,"slug":264,"hasResults":11,"nctId":265,"briefTitle":266,"officialTitle":267,"acronym":4,"eligibilityCriteria":268,"healthyVolunteers":118,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":269,"targetDuration":4,"studyType":23,"phases":271,"briefSummary":272,"conditions":273,"keywords":276,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":278,"lastUpdatePostDateStruct":279,"startDateStruct":281,"completionDateStruct":282,"leadSponsor":284,"locationsCount":4},"100554949","postnatal-companion-support-the-effect-of-education-on-maternal-depression-and-fatigue-100554949","NCT06505733","Postnatal Companion Support The Effect of Education on Maternal Depression and Fatigue","Postnatal Companion Support The Effect of Education on Maternal Depression and Fatigue: A Randomised Controlled Trial","Inclusion Criteria:\n\n* Knowing how to read and write Turkish,\n* Volunteer to participate in the research,\n* She gave birth by cesarean section,\n* Primiparous,\n* Pregnant women who are open to communication (able to understand and answer questions) will be included in the sample.\n\nExclusion Criteria:\n\n* Those who do not have the skills of reading, listening, writing, speaking and understanding Turkish,\n* Those who have a hearing or visual impairment,\n* Having postpartum complications,\n* giving birth to stillbirth,\n* People who wanted to withdraw from the study were not included.",{"count":270,"type":22},72,[25],"In this study, it is aimed to investigate the effect of the trainings included in the content of the practical guide for postpartum supporter training companions, which will be given to the companions of women in the postpartum period, on depression and fatigue on mothers. The research will be conducted in methodological and single blind randomised control design. The study will be conducted at Necmettin Erbakan University Faculty of Medicine Hospital. A total of 70 puerperants will be included in the study as intervention (n: 35) and control (n: 35) groups. Introductory Information Form, Postpartum depression rating scale as data collection tools in the study: Motherhood Monitoring Scale by Parents (MMSP), Edinburgh Postnatal Depression Scale (EDDS), Multidimensional Fatigue Rating Scale will be used. The research data will be collected three times as pre-test data, fourth day and tenth day. Number, percentage, mean and standard deviation will be used in the evaluation of descriptive data; Chi-square test will be used for the similarity of the descriptive characteristics of the experimental and control groups; Kolmogrow-Smirnov and Shapiro-Wilk will be used in the normality analysis of dependent variables; t test in independent groups (student t test) will be used to compare the post-test scores of the experimental and control groups; and ANOVA in dependent groups will be used to compare the pre-test-post-test mean scores of the experimental group and eta square will be used to calculate effect sizes. The results obtained will be tested at p\\\u003C0.05 significance level and bidirectionally. When the literature is examined, there is not enough data on the depression and fatigue of the companion caring for the woman in the postpartum period. This study aims to fill the gaps in the literature and to reduce depression and fatigue in mothers.",[274,275,155,32],"Postpartum","Fatigue",[277,155,275,274],"social support","2024-08-07",{"date":280,"type":42},"2024-08-09",{"date":278,"type":22},{"date":283,"type":22},"2024-08-17",{"name":285,"class":49},"KTO Karatay University"]