[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"behavioral-problem\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:behavioral-problem":35},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,56,79],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":36,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100479368","reducing-blood-pressure-in-mid-life-adult-binge-drinkers-100479368",false,"NCT05522075","Reducing Blood Pressure in Mid-life Adult Binge Drinkers","Reducing Blood Pressure in Mid-life Adult Binge Drinkers: the Role of Microvascular Function and Sympathetic Activity","Inclusion Criteria:\n\n* Men and women (50-64 years of age) who do not drink alcohol, who drink at moderate levels, or who binge drink\n* Female subjects will be postmenopausal (i.e., cessation of menses for ≥1 yr).\n* Subjects who can speak and understand English.\n\nExclusion Criteria:\n\n* a history of diabetes, cardiovascular disease, liver, or renal disease\n* current or history of smoking and illicit drug use\n* blood pressure ≥160\u002F100 mm Hg\n* other known traditional cardiovascular disease risks: obesity (BMI≥35 kg\u002Fm2), or hyperlipidemia (total cholesterol\\>230 mg\u002Fdl and\u002For LDL cholesterol\\>160 mg\u002Fdl)\n* active infection (in the past 2 months)\n* a history of seizures, cancer, or inflammatory disease (i.e., gout or rheumatoid)\n* unstable body weight (\\>5% change during the past 6 months)\n* regular aerobic exercise training (i.e., they engage in 30 min of structured aerobic exercise at least 3 times per week)\n* current use of hormone replacement therapy (i.e., estrogen, progesterone, and testosterone)",true,"ALL","50 Years","64 Years",{"count":21,"type":22},55,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study has two phases:\n\nPhase 1 is to examine blood pressure, microvascular function, and sympathetic nerve activity in mid-life adult binge drinkers vs. alcohol abstainers\u002Fmoderate drinkers.\n\nPhase 2 is to examine the effect of 8-week aerobic exercise training on blood pressure, microvascular function, and sympathetic nerve activity in mid-life adult binge drinkers",[28,29,30,31,32,33,34,35],"Alcohol Drinking","Binge Drinking","Blood Pressure","Alcohol Abstinence","Aging","Lifestyle Factors","Vasodilation","Behavioral Problem",[37,38,39,40,41,42],"Exercise training","High-intensity interval training","Midlife adults","Middle-aged","Microvascular function","Sympathetic nerve activity","RECRUITING","2026-05-27",{"date":46,"type":47},"2026-06-01","ACTUAL",{"date":49,"type":47},"2022-11-21",{"date":51,"type":22},"2027-04-30",{"name":53,"class":54},"The University of Texas at Arlington","OTHER",1,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":23,"phases":66,"briefSummary":67,"conditions":68,"keywords":4,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":55},"100569547","referral-training-and-egen-trials-100569547","NCT06695663","Referral Training and eGen Trials","Inclusion Criteria:\n\n* Inclusion criteria for parent in the randomized controlled trial include being a parent or caregiver of a child ages 3 to 8 and having a referral to a participating therapist from a primary care provider.\n* The only inclusion criteria is that participants be a PCC who sees children between the ages of 3- 8 years old. PCCs must also have approval from their clinic to participate. Vulnerable populations will not be targeted from inclusion but may be included if they meet the previously stated inclusion criteria.\n\nExclusion Criteria:\n\n* Parents would be excluded if there is a reasonable belief that participating could increase danger to a child or if they are psychologically unable to engage in the intervention activities.","18 Years","100 Years",{"count":65,"type":22},600,[25],"Child and adolescent behavioral health problems are related to the leading causes of youth morbidity and mortality. Parent-focused interventions effectively prevent behavioral health problems such as depression and conduct disorders and can provide a downstream economic benefit to society by reducing criminal activity, education costs, and health care use.\n\nUnfortunately, parenting programs are not widely available, accessible, nor well-attended.\n\nPediatric primary care is a non-stigmatizing setting with nearly universal reach and, therefore, an ideal contact point to increase access. However, primary care clinicians (PCCs) often have insufficient training in behavioral health topics and typical referral practices are inadequate.\n\nThere are also logistical barriers to attending in-person parenting programs, like the need for childcare and a large time-commitment. There is a need to develop effective referral practices in conjunction with increasing the accessibility of parenting programs. The study long-term goal is to prevent significant behavioral health problems through widespread access to effective and accessible parenting programs through primary care referrals.\n\nIn this study there are two trials: First is the primary care clinicians \"PCC\" trial, testing the effectiveness of referral training (aim 1). Second is the parents \"eGen\" trial provided by therapists, testing the effectiveness of eGen parenting intervention (aim 2).",[35,69],"Behavioral Problem of Child","2025-12-11",{"date":72,"type":47},"2025-12-15",{"date":74,"type":47},"2025-01-17",{"date":76,"type":22},"2030-11-01",{"name":78,"class":54},"University of Minnesota",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":16,"sex":17,"minAge":86,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":96,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":55},"100554968","stop-focus-plan-and-change-predicting-parent-and-child-responses-to-a-brief-telehealth-parent-training-100554968","NCT06505980","Stop, Focus, Plan, and Change: Predicting Parent and Child Responses to a Brief, Telehealth Parent Training","Stop, Focus, Plan, and Change: A Translational Approach to Predict Parent and Child Responses to a Brief, Telehealth Parent Training","Inclusion Criteria:\n\n* Parent speaks English or Spanish\n* Parent has access to Internet\n* Parent intends to complete treatment\n* Parent reports child has elevated externalizing concerns\n\nExclusion Criteria:\n\n* Child is a ward of the state\n* Child diagnosed with severe medical or nonverbal developmental disability","3 Years","5 Years",{"count":89,"type":22},130,[25],"This study will look at who does not improve after doing a behavioral parent training program briefly through telehealth. It will also study ways to make the intervention better for those that do not improve.",[35,93,94,95],"Irritable Mood","Parenting","Stress",[97,98,99,100],"Behavioral Concerns","Irritability","Parenting stress","Parenting practices","2025-02-28",{"date":103,"type":47},"2025-03-04",{"date":105,"type":47},"2024-10-18",{"date":107,"type":22},"2029-03-30",{"name":109,"class":54},"University of Colorado, Denver"]