[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"engagement-patient\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:engagement-patient":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,52,88,114,144,169,200],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":34,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100609439","nicu-utilization-of-remote-voice-technology-to-improve-maternal-experience-nurture-100609439",false,"NCT07214597","NICU Utilization of Remote Voice Technology to Improve mateRnal Experience (NURTURE)","NICU Utilization of Remote Voice Technology to Improve mateRnal Experience (NURTURE): A Randomized Controlled Trial","NURTURE","Inclusion Criteria:\n\n1. Infant:\n\n   1. Admitted to the neonatal intensive care unit (NICU)\n   2. Not readmitted after discharge from the NICU\n   3. Expected to survive at least 2 weeks\n   4. Expected to be admitted to the NICU for at least 2 weeks\n   5. Singleton gestation\n2. Mother:\n\n   1. Age ≥ 18 years old\n   2. English speaking\n   3. Mother is the biological mother of the infant admitted to the NICU\n   4. Postpartum day 4 or less\n3. Partner (NOTE: Partner enrollment is not required)\n\n   1. Mother agrees to partner's participation\n   2. Designated by mother as support person with infant access\n\nExclusion Criteria\n\n1. Infant\n\n   a. Re-admission to NICU\n2. Mother\n\n   1. No access to an Android or iOS smartphone\n   2. Unwilling to download the VoiceLove NICU app to their personal smartphone and unwilling to accept the terms and conditions of the VoiceLove app\n   3. No personal email address\n   4. Incarcerated at time of delivery or postpartum\n   5. Inability to obtain informed consent\n\n   i. Patient's clinician refuses enrollment of the patient ii. Patient is either mentally (acute psychosis) or physically (intubated or critically ill in the ICU) unable to provide informed consent f. Unable to approach the patient (staffing, patient unavailable) g. Mother is not the intended parent (plans adoption, is a surrogate, will not have custody of the infant)\n3. Partner (NOTE: Partner enrollment is not required)\n\n   1. Age \\\u003C 18 years old\n   2. Not English speaking\n   3. Inability to obtain informed consent\n   4. No access to an Android or iOS smartphone that is different from the mother's smartphone\n   5. No access to an email address that is different from the mother's email address\n   6. Unwilling to download the VoiceLove NICU app to their personal smartphone and unwilling to accept the terms and conditions of the VoiceLove app",true,"FEMALE","18 Years",{"count":21,"type":22},150,"ESTIMATED","INTERVENTIONAL",[25],"NA","The study's objective is to conduct a Phase II randomized controlled trial examining the preliminary efficacy of the VoiceLove app compared to usual care on maternal postpartum depression in mothers with infants admitted to the Neonatal Intensive Care Unit (NICU). Primary aim: Assess the effects of VoiceLove on maternal postpartum depression, measured by the Edinburgh Postnatal Depression Scale (EPDS). The estimates from this study will be used for a future definitive Phase III trial. Secondary aim: Assess feasibility, acceptability, and patterns of communication and engagement among mothers, partners, and NICU clinicians during the NICU hospitalization, measured through app usage metrics, satisfaction surveys, and qualitative interviews. Additionally, we will evaluate effects of infant length of stay.",[28,29,30,31,32,33],"Postpartum Depression (PPD)","Self-Efficacy","Parental Anxiety","Engagement, Patient","Usability","Length of Stay",[35,36,28,37,15,38],"Neonatal Intensive Care Unit","NICU","VoiceLove app","VoiceLove","RECRUITING","2026-06-15",{"date":42,"type":43},"2026-06-17","ACTUAL",{"date":45,"type":43},"2026-02-04",{"date":47,"type":22},"2028-01",{"name":49,"class":50},"Vanderbilt University Medical Center","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":60,"minAge":61,"maxAge":19,"enrollmentInfo":62,"targetDuration":4,"studyType":23,"phases":64,"briefSummary":65,"conditions":66,"keywords":73,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":51},"100608922","parents-helping-parents-for-youth-vaping-cessation-100608922","NCT07207850","Parents Helping Parents for Youth Vaping Cessation","Parents Helping Parents for Youth Vaping Cessation (PhP-VX)","PhP-VX","ADOLESCENT INCLUSION:\n\n* 15-18\n* Report vaping in the previous 30 days\n* English literacy\n\nPARENT INCLUSION:\n\n* Biological, adoptive, stepparents, or adult guardian of adolescent participating\n* Have face-to-face contact with the adolescent at least one day per week during the study period\n* Access to a computer or mobile phone at home\n* Interested in helping adolescent quit e-cigarette\u002Fvape use","ALL","15 Years",{"count":63,"type":22},200,[25],"The goal of this randomized controlled study is to test if this new intervention works to help adolescents quit vaping. A key feature of the program is the use of peer support for parents, delivered by trained parent coaches. Participants will complete baseline and follow up surveys. Parents in the intervention arm will receive peer support as part of the program.",[67,31,68,69,70,71,72],"Implementation Science","E Cigarette Use","Peer Support","Vaping Teens","Vaping Cessation","Parent Support",[74,75,76,77,78],"Vaping","Tobacco","vaping cessation","Parent support","adolescent vaping","2026-05-20",{"date":81,"type":43},"2026-05-26",{"date":83,"type":43},"2026-05-18",{"date":85,"type":22},"2027-08-31",{"name":87,"class":50},"University of Nebraska",{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":94,"eligibilityCriteria":95,"healthyVolunteers":17,"sex":60,"minAge":96,"maxAge":4,"enrollmentInfo":97,"targetDuration":4,"studyType":23,"phases":99,"briefSummary":100,"conditions":101,"keywords":102,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":113},"100614374","qt-digital-mental-health-engagement-study-100614374","NCT07278765","QT-Digital Mental Health Engagement Study","Optimizing Engagement With Digital Mental Health Services Among Sexual And Gender Minority Consumers","QT-DIMES","Inclusion Criteria:\n\n* Users of the Mental Health America (MHA) website engaging from Internet Protocol (IP) addresses in the United States\n* Completed the PHQ-9 depression screener in English\n* Answered MHA's standard demographic questions that identify users as age 14 and older\n* Answered MHA's standard demographic questions that identify users as LGBTQ+.\n\nExclusion Criteria:\n\n* IP addresses outside of the United States\n* Do not answer MHA's standard demographic questions\n* Answered MHA's standard demographic questions that identify users as age 13 and younger\n* Answered MHA's standard demographic questions that identify users as not LGBTQ+.","14 Years",{"count":98,"type":22},2300,[25],"Sexual and gender minority (SGM) populations are disproportionately impacted by mental health concerns relative to their heterosexual and cisgender peers. Despite high need, SGM populations continue to report unmet mental health needs because they cannot or do not access mental health services. Digital Mental Health (DMH) services have been recognized as feasible, economical, and effective options to broaden the availability of mental health care to consumers who face barriers to mental health help-seeking. SGM consumers cite a preference for DMH care and this delivery format holds promise to attend to major mental health care access barriers experienced by this consumer group. Yet, the availability of DMH services tailored to the needs of SGM consumers is limited, and a dearth of research examines SGM populations' actual engagement with DMH services. A potential solution to fully understand how SGM populations utilize DMH services would be to characterize their engagement within a natural setting. Leveraging an established partnership with Mental Health America (MHA), a non-profit mental health advocacy group offering free, evidence-based screenings and self-guided DMH resources, this study will follow a large, naturalistic sample of SGM DMH consumers with the aim to test tailored engagement strategies with SGM DMH consumers using a micro-randomized trial (MRT) design. Results of this study will inform if delivering engagement strategies can meaningfully increase initial and sustained engagement with MHA resources and which types of strategies, specifically, work best for which users.",[31],[103],"Digital Mental Health","2026-05-06",{"date":106,"type":43},"2026-05-08",{"date":108,"type":43},"2026-03-12",{"date":110,"type":22},"2027-05",{"name":112,"class":50},"University of Washington",2,{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":119,"acronym":4,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":121,"targetDuration":4,"studyType":23,"phases":123,"briefSummary":124,"conditions":125,"keywords":130,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":51},"100486003","1morestep-an-intervention-to-increase-hiv-care-engagement-and-reduce-intimate-partner-violence-among-black-women-living-with-hiv-100486003","NCT05608421","1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV","1MoreStep: Pilot Trial of an Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV","Inclusion Criteria:\n\n* Cis-gender female\n* Black or African American\n* ≥ Age 18\n* Living with HIV\n* ≤ 1 HIV care visit in previous 12 months OR virally unsuppressed (\\>50 copies\u002FmL) OR at high risk for poor HIV care adherence (PHQ ≥ 3, Generalized Anxiety Disorder (GAD) ≥ 3, active substance use)\n* IPV within the previous 2 years\n* Ability to attend in-person for up to 8 sessions\n* Do not report immediate severe danger from their partner\n* English fluency\n\nExclusion Criteria:\n\n* Not a Cis-gender female\n* Not Black or African American\n* ≤ Age17 or younger\n* Not living with HIV\n* ≥ 2 HIV care visits in previous 12 months\n* No IPV within the previous 2 years\n* Inability to attend in-person for up to 8 sessions\n* Reports immediate severe danger from their partner\n* Not fluent in English",{"count":122,"type":22},100,[25],"This study tests a 5-session cognitive behavioral approach program (herein referred to as the 1MoreStep intervention) to train Black women living with HIV (BWLWHI) and exposed to intimate partner violence (IPV) in the past 2 years (hereafter, BWLWHI) in: 1) cognitive and behavioral skills to access internal and external sources of strength (e.g. self-reliance, safety net); safety strategies, knowledge about Undetectable = Untransmissible (U=U) and HIV care; and reduce internalized and anticipated stigma; 2) communication skills to respond to enacted HIV and IPV stigma and enlist social support; and 3) addressing structural barriers to HIV care engagement with an HIV navigator component. The intervention is informed by the HIV-Stigma Framework and a resilient-reintegration model which views women as active participants in responding to IPV and managing life with HIV.\n\nAim 1: Examine preliminary efficacy of the 1MoreStep intervention on: (a) IPV safety strategies (informal and formal resources, safety planning, and placating strategies at baseline, 3-month and 6-month follow-up visits); and (b) HIV care engagement (medical record confirmed visit with an HIV care provider, antiretroviral therapy (ART) prescription, medication adherence, and viral load status during 3-month and 6-month follow-up visits).\n\nAim 2: Examine the acceptability and feasibility of the 1MoreStep intervention operationalized by (a) quantitative measures: session attendance and fidelity to key intervention components and (b) qualitative interviews to assess: program fit, facilitators and barriers to participation, and using 1MoreStep intervention skills.",[126,127,128,31,129],"Violence, Domestic","HIV","Stigma, Social","Medication Adherence",[127,131,132,133,134],"Intimate Partner Violence (IPV)","Black women","Cognitive behavioral approach","Randomized Control Trial (RCT)","2026-04-23",{"date":137,"type":43},"2026-04-29",{"date":139,"type":43},"2023-06-26",{"date":141,"type":22},"2026-12",{"name":143,"class":50},"Johns Hopkins University",{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":150,"eligibilityCriteria":151,"healthyVolunteers":11,"sex":60,"minAge":152,"maxAge":4,"enrollmentInfo":153,"targetDuration":4,"studyType":23,"phases":155,"briefSummary":156,"conditions":157,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":51},"100630548","forge-ahead-feasibility-of-yoga-to-improve-cognitive-function-100630548","NCT07489105","Forge AHEAD: Feasibility of Yoga to Improve Cognitive Function","Engaging Stakeholders and Patients to Evaluate the Feasibility of Yoga to Improve Cognitive Function in Rural Heart Failure Patients in the Deep South","Forge AHEAD","Inclusion Criteria:\n\n* Heart failure diagnosis\n* Aged 55 years or older\n\nExclusion Criteria:\n\n* Traumatic brain injury, co-existing neurological and psychiatric disorders\n* Implanted defibrillator or metal objects, left ventricular assist device placement, or cardiac transplant\n* Substance abuse\n* Unable to perform yoga due to physical limitations or severity of illness\n* Currently engaged in a yoga program","55 Years",{"count":154,"type":22},20,[25],"The investigators will conduct a two-phase pilot study to test the feasibility and acceptability of a 12-week Chair Yoga intervention for 20 heart-failure patients. Using a patient-centered approach, investigators will involve stakeholders in designing the protocol, gather patient feedback, and refine the protocol accordingly.",[158,159,31],"Heart Failure","Rural Health","2026-03-21",{"date":162,"type":43},"2026-03-25",{"date":164,"type":43},"2025-07-24",{"date":166,"type":22},"2027-12-31",{"name":168,"class":50},"Auburn University",{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":4,"eligibilityCriteria":175,"healthyVolunteers":11,"sex":60,"minAge":176,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":23,"phases":180,"briefSummary":181,"conditions":182,"keywords":186,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":51},"100587644","otago-exercise-program-and-motivational-interviewing-100587644","NCT06931067","OTAGO Exercise Program and Motivational Interviewing","Health Behavior Change for Fall Prevention","Inclusion Criteria:\n\n* Age ≥60\n* At high fall risk: At least one \"Yes\" to 1) had a fall in the past year; 2) answer \"difficult\" to the question \"do you find it hard to stand without using your hands\"; 3) worry about falling\n* Able to converse audibly and coherently in English\n* Ambulatory with or without assistive device use\n* Self-report challenges navigating the environment outside of the home\n* At least one \"some or much difficulty\" or \"unable to do\" to:Walking one block?; Stepping up onto a curb?; Getting out of a straight back chair? Climbing one flight of stairs? Getting out of the house\n\nExclusion Criteria:\n\n* o Receiving ongoing physical therapy with a primary focus on improving balance and strength of lower extremities\n\n  * Experiencing acute health issues such as fracture, pain, or infection that prohibits them from participating in exercises\n  * Able to stand on one foot for more than 10 seconds without holding onto something\n  * 6-item Callahan cognitive assessment over the phone: Patients with scores of 2 or less, positive for dementia criteria, will be excluded.\n  * Patients participating in other studies that may impact fall-related behavior change.\n  * Participants engaged in routine moderate or vigorous physical activities that require lower extremity balance and strength (e.g., \\>100 minutes\u002Fweek for more than 3 months)","60 Years","120 Years",{"count":179,"type":22},60,[25],"The goal of this study is to see if OTAGO instructors, who have been trained in a special communication method called motivational interviewing, can help older adults start and stick with the OTAGO exercise program. The results will help guide future research on how behavior change techniques can support other fall prevention strategies.",[183,184,31,185],"Fall Risk Factors","Physical Activity","Community-dwelling Older Adults",[187,188,189,190],"OTAGO","OEP","Motivational interviewing","behavior change","2025-04-09",{"date":193,"type":43},"2025-04-16",{"date":195,"type":43},"2025-02-20",{"date":197,"type":22},"2026-02",{"name":199,"class":50},"Oregon Health and Science University",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":204,"acronym":205,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":60,"minAge":19,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":23,"phases":209,"briefSummary":210,"conditions":211,"keywords":215,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":230},"100560318","digital-navigators-for-acceptance-and-competence-development-with-mental-health-apps-100560318","NCT06575582","Digital Navigators for Acceptance and Competence Development with Mental Health Apps","DigiNavi","Inclusion Criteria:\n\n* Main diagnosis according to ICD 10 F00-F69, F80-F99\n* Capacity to consent is given\n* Sufficient language skills for an interview in German\n* Participants have access to modern digital hardware (smartphone)\n* Basic knowledge of how to operate a smartphone\n\nExclusion Criteria:\n\n* Acute danger to self or others\n* Patients have received prompt (\\\u003C= 3 weeks) qualified psychiatric or psychotherapeutic treatment\n* Severe organic brain diseases with cognitive deficits\n* Intellectual disability",{"count":208,"type":22},116,[25],"The goal of this clinical trial is to learn if and how so called \"Digital Navigators\" (DN) can help general practitioners, outpatient psychiatrists and psychologists as well as their treated patients to use digital mental health apps (DiGAs) and integrate it into their treatment. The main questions it aims to answer are:\n\n* What are the chances and implementation barriers of DN?\n* What are the acceptance and expectations towards DN?\n* Do DN affect the psychological health of patients?\n* Do DN affect the digital health literacy and technical competence of participants?\n\nEmployees of medical teams (e.g. medical assistants) receive training to become a DN. Afterwards patients are accompanied and supported by the DN for 12 weeks to select and use a suitable app for their mental disorder.",[212,31,213,214],"Acceptability of Health Care","Nurse's Role","Mental Disorder",[216,217,218,219,220],"digital health","ehealth","mhealth","mental health","health literacy","2024-08-29",{"date":223,"type":43},"2024-09-03",{"date":225,"type":43},"2024-07-15",{"date":227,"type":22},"2025-07-14",{"name":229,"class":50},"Medizinische Hochschule Brandenburg Theodor Fontane",6]