[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"anger\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:anger":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,48,74,106,136,167,203,228,259,283,312],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100578511","therapy-dog-visits-for-patients-hospitalized-with-traumatic-injuries-100578511",false,"NCT06812247","Therapy Dog Visits for Patients Hospitalized With Traumatic Injuries","Inclusion Criteria:\n\n* Patients admitted to the Trauma and Acute Care Surgery (TACS) service following a trauma\n* English or Spanish speaking\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Fear of dogs, allergy to dogs\n* Immunocompromised\n* Contact precautions\n* Delirious, intubated, or otherwise unable to consent","ALL","18 Years",{"count":18,"type":19},80,"ESTIMATED","INTERVENTIONAL",[22],"NA","Animal assisted therapy (AAT) with dogs has been shown to be beneficial for a wide range of patients with both acute and chronic illnesses, including spinal cord injuries, heart failure, myocardial infarctions, strokes, cancer, post-traumatic stress disorder, and depression. Studies have also demonstrated that even in healthy adults, the presence of dogs is associated with physiologic changes such as increased pain threshold, decreased blood pressure, and decreased heart rate. However, few studies have investigated the role of AAT in the post-operative course in adults. This study will investigate the impact of therapy dog visits on pain and anxiety scores for trauma patients at Boston Medical Center (BMC).",[25,26,27,28,29],"Trauma Injury","Depression","Anxiety","Anger","Pain",[31,32,33,34],"Therapy dogs","Healing pups","Animal assisted therapy (AAT)","Traumatic injuries recovery","RECRUITING","2026-06-13",{"date":38,"type":39},"2026-06-16","ACTUAL",{"date":41,"type":39},"2025-06-04",{"date":43,"type":19},"2026-12",{"name":45,"class":46},"Boston Medical Center","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":16,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":20,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":47},"100637110","examining-the-efficacy-of-the-man-therapy-platform-in-reducing-problematic-anger-among-military-service-members-with-and-without-a-tbi-history-100637110","NCT07604701","Examining the Efficacy of the Man Therapy Platform in Reducing Problematic Anger Among Military Service Members With and Without a TBI History","Examining the Efficacy of the Man Therapy Platform in Reducing Problematic Anger Among Military Service Members With and Without a TBI History: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Military service member\n* Identify as male\n* Aged 18+ years\n* Positive problematic anger screen (DAR-3 \\>8)\n* Ability to read, write, and speak English\n\nExclusion Criteria:\n\n* Active psychosis or acute mania necessitating clinical intervention\n* Acute thoughts of self- or other-harm necessitating imminent clinical intervention (e.g., hospitalization)\n* Unable to provide informed consent","MALE",{"count":57,"type":19},226,[22],"The goal of this randomized controlled trial is to determine if an interactive digital solution, Man Therapy, reduces indices of problematic anger in male military service members who screen positive for problematic anger.\n\nThe man questions this study aims to answer are:\n\n* Does Man Therapy reduce indices of problematic anger?\n* Does Man Therapy reduce psychosocial correlates of anger?\n\nResearchers will also examine if the effects of those aims differ based on a participant's history of a mild TBI, the mechanism of a primary mild TBI, and\u002For the number of mild TBIs.\n\nResearchers will compare Man Therapy to a waitlist control. This will help determine if Man Therapy works better than no treatment.\n\nParticipants will:\n\n* Complete a baseline survey\n* Be randomized to intervention or waitlist control\n* If randomized to intervention, participants will receive the intervention and complete a survey immediately after the intervention and at 1-, and 3-months following the intervention\n* If randomized to waitlist control, participants complete surveys at 1-, and 3-months and have the opportunity to complete the intervention following the 3-month survey",[61,62,28],"Mild Traumatic Brain Injury (mTBI)","Traumatic Brain Injury",[62,28],"NOT_YET_RECRUITING","2026-05-26",{"date":67,"type":39},"2026-05-29",{"date":69,"type":19},"2026-09-01",{"date":71,"type":19},"2028-12-01",{"name":73,"class":46},"University of Colorado, Denver",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":15,"minAge":81,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":20,"phases":85,"briefSummary":86,"conditions":87,"keywords":93,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":47},"100585460","step-by-step-evaluation-of-a-stepped-care-model-100585460","NCT06902649","Step-by-Step: Evaluation of a Stepped Care Model","Step-by-Step: Evaluation of a Stepped Care Model for Anger, Defiant, or Aggressive Behavior in Children and Adolescents","Inclusion Criteria:\n\n* Families with children aged 8-16 years who have difficulty controlling anger or exhibit defiant or aggressive behavior. The child\u002Fadolescent meets 3 of the diagnostic criteria for Oppositional Defiant Disorder or 2 criteria for Conduct Disorder indicating aggressive behavior.\n* Medication for the child can remain stable.\n* Parents need to be able to read and engage with materials in Swedish\n\nExclusion Criteria:\n\n* Families with children younger than 8 years old or who have already turned 17, or who do not exhibit defiant or aggressive behaviors according to the first inclusion criterion.\n* Children with severe depression, suicidal behavior, bipolar disorder, psychosis, eating disorders, severe autism (level 2 and 3), diagnosed intellectual disability, or ongoing criminal behavior assessed to require interventions other than the study's interventions are excluded.\n* Children\u002Fadolescents with other ongoing psychological treatments for the same condition or assessed by the clinician in need of other interventions\n* Parents and children with epilepsy or migraines","8 Years","16 Years",{"count":84,"type":19},210,[22],"The primary aim of this project is to examine the effectiveness of a stepped care model of interventions for children's defiant or aggressive behavior problems. The stepped model consists of a brief internet-based parenting support program (Step 1). For those with continued need of additional interventions, Step 2 includes access to one of following interventions: b) a Cognitive Behavior Therapy (CBT) -Virtual Reality (VR)-assisted parenting support program, b) a Cognitive Behavior Therapy -Virtual Reality-assisted child intervention, or c) standard interventions\u002Fsupport at the family's unit\u002Fclinic and continued access to the study's internet-based parenting support program, after which the family may choose CBT-VR for the child or the parent.",[88,89,90,91,92,28],"Child Behavior Problem","Disruptive Behavior","Oppositional Defiant Disorder","Conduct Problems","Aggression",[89,88,94,95,96],"Cognitive behavior therapy","Virtual Reality","Parenting support program","2026-03-04",{"date":99,"type":39},"2026-03-06",{"date":101,"type":39},"2025-04-02",{"date":103,"type":19},"2027-08-31",{"name":105,"class":46},"Karolinska Institutet",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":110,"acronym":111,"eligibilityCriteria":112,"healthyVolunteers":113,"sex":15,"minAge":16,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":20,"phases":117,"briefSummary":118,"conditions":119,"keywords":125,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":128,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":47},"100515759","a-mixed-methods-pilot-trial-of-the-step-home-workshop-to-improve-reintegration-and-reduce-suicide-risk-for-recently-transitioned-veterans-100515759","NCT05995678","A Mixed Methods Pilot Trial of the STEP Home Workshop to Improve Reintegration and Reduce Suicide Risk for Recently Transitioned Veterans","SH-SP","Inclusion Criteria:\n\n* Recently transitioned Veterans within three years of separation from military service\n* Self-reported functional impairment or reintegration difficulties as measured by the Military-to-Civilian Questionnaire (any item score \\> 1 indicating \"some difficulty\"; M2CQ; \\[71\\])\n* Sufficient English fluency\n* Agree to participate (informed consent\u002FHIPAA)\n\nExclusion Criteria:\n\n* Active psychosis\n* Imminent or acute high suicide risk requiring immediate crisis intervention (low-moderate non-imminent risk for suicide is allowed)\n* Current moderate or severe substance use disorder\n* Neurological diagnosis excluding TBI\n\n  * Participants with mild substance use disorder will be allowed\n  * Substance use is a common behavior that may contribute to reintegration difficulties and suicide risk",true,"65 Years",{"count":116,"type":19},120,[22],"Risk of Veteran suicide is elevated during the first year of transition from military service to civilian life. Most Veteran suicides occur among Veterans who are not connected to VA healthcare. Suicide prevention and connection to care are therefore critical for recently transitioning Veterans. Transitioning Veterans require services to provide them with suicide prevention education, skills to manage their transition effectively, and support in their access to VA healthcare. Convenient, accessible, palatable, patient-centered care options that are cost-effective, easy to implement nationwide, and target domains known to mitigate suicide risk are needed during this critical transition period. This proposal would bridge this important healthcare gap using STEP-Home-SP, a transdiagnostic, non-stigmatizing, skills-based workshop. STEP-Home-SP will provide Veterans with suicide prevention education, skills to improve transition, support to access VA care, and a platform to decrease social isolation early in their military to civilian transition, thereby reducing suicide risk downstream.",[120,121,122,123,124,28],"TBI","Suicide Prevention","Veterans","PTSD","Transdiagnostic",[122,120,124,126,121,123,127],"Intervention","Reintegration",{"date":99,"type":39},{"date":130,"type":39},"2024-03-01",{"date":132,"type":19},"2027-05-31",{"name":134,"class":135},"VA Office of Research and Development","FED",{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":142,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":15,"minAge":144,"maxAge":145,"enrollmentInfo":146,"targetDuration":4,"studyType":20,"phases":148,"briefSummary":149,"conditions":150,"keywords":153,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":47},"100517647","parent-management-training-to-treat-irritability-100517647","NCT06020261","Parent Management Training to Treat Irritability","The Efficacy of Parent Management Training to Treat Irritability","PMT","Inclusion Criteria:\n\n* clinically significant irritability (Clinician Affective Reactivity Index 30 or greater)\n* parent or guardian willing to participate in treatment with the child\n\nExclusion Criteria:\n\n* psychiatric instability (danger to self\u002Fothers, risky substance abuse)\n* current active Post-Traumatic Stress Disorder (PTSD) or a severe active stressor (e.g. child abuse)\n* history of severe psychopathology with an established alternate treatment (e.g. autism spectrum disorder, bipolar disorder, schizophrenia, intellectual disability)\n* general medical condition that may be driving irritability or prevent generalizable physiologic measures.\n* screen positive for an intellectual disability via Wechsler Abbreviated Scale of Intelligence Second Edition (WASI II) estimated Intelligence Quotient (IQ)\\\u003C70.","10 Years","14 Years",{"count":147,"type":19},36,[22],"The goal of this clinical trial is to see if 12 sessions of a Parent Management Training program can treat irritability in children aged 10-14 years old. The main question it aims to answer are:\n\n* Can a Parent Management Training for parents reduce anger outbursts and cranky moods in their children?\n* Can Parent Management Training be done in an outpatient clinic and do parents like it?\n\nUp to 18 families can join this study. This study will be used to set up a larger study in the Fall of 2025.\n\nParent participants will complete 12 sessions of Parent Management Training for Irritability. Each session will be 45-55 minutes weekly. They will also participate in the assessments of their child before, during and after treatment.\n\nChild participants will do assessments before, during and after the Parent Management Training treatment.",[151,152,28],"Irritable Mood","Temper Tantrum",[154,155,156,157,158],"irritability","anger","parenting","temper outbursts","Parent Management Training","2026-01-06",{"date":161,"type":39},"2026-01-07",{"date":163,"type":39},"2025-06-12",{"date":165,"type":19},"2026-12-30",{"name":73,"class":46},{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":20,"phases":176,"briefSummary":177,"conditions":178,"keywords":191,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":202},"100471118","art-therapy-and-emotional-well-being-in-military-populations-with-posttraumatic-stress-symptoms-100471118","NCT05414708","Art Therapy and Emotional Well Being in Military Populations With Posttraumatic Stress Symptoms","Inclusion Criteria:\n\n* DEERS Eligible\n* Active Duty or Veteran separated within the past 10 years\n* Significant posttraumatic stress symptoms (score of \\>\u002F=31 on the PCL-5)\n\nExclusion Criteria:\n\n* History of moderate, severe, or penetrating brain injury\n* History of psychotic disorder, bipolar disorder, or active suicidal or homicidal ideation\n* History of multiple sclerosis, Huntington's disease, or Alzheimer's disease\n* History of stroke or myocardial infarction\n* History of brain tumor\n* History of seizures\n* Contradictions for MRI (for example, participants will be excluded for pregnancy, metal implants or suspected shrapnel, aneurysm\u002Fintracranial clips, cardiac pacemakers or implanted programmable devices or pumps)\n* Unable to provide informed consent\n* History of previous exposure to art therapy\n* Active substance use disorder","64 Years",{"count":175,"type":19},40,[22],"Art therapy is used across the Military Health System for treatment of posttraumatic symptoms, but there is limited research on how art therapy is able to restore emotional expression and regulation in service members. This research hopes to learn about the effects of art therapy on emotional expression and regulation in service members as well as the neurological systems at work. If a participant chooses to be in this study, he or she will attend eleven sessions over a period of six to eight months. The first session will be an interview and self-assessment questionnaires to collect information on a variety of symptoms, experiences, and personality traits, and an MRI scan. During the MRI scan, participants will be asked to perform a task where they will be shown a series of neutral and negative images. The following eight sessions will be one-hour art therapy sessions with a certified art therapist. The tenth session will consist of the same self-assessment questionnaires and another MRI scan. The final session will consist of some of the same questionnaires from the tenth visit, as well as a qualitative interview done virtually three months after the tenth visit.",[123,179,180,181,182,183,184,151,28,185,186,187,188,189,190],"Military Activity","Post-Traumatic Headache","Posttraumatic Stress Disorder","Posttraumatic Stress Disorder, Delayed Onset","Sleep Disturbance","Nightmare","Combat and Operational Stress Reaction","Combat Stress Disorders","Military Family","Military Operations","Emotional Regulation","Emotion Processing",[123,192,193],"Military","Art Therapy",{"date":195,"type":39},"2026-01-08",{"date":197,"type":39},"2022-02-01",{"date":199,"type":19},"2027-12",{"name":201,"class":135},"Walter Reed National Military Medical Center",2,{"id":204,"slug":205,"hasResults":11,"nctId":206,"briefTitle":207,"officialTitle":208,"acronym":209,"eligibilityCriteria":210,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":211,"targetDuration":4,"studyType":20,"phases":213,"briefSummary":214,"conditions":215,"keywords":216,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":47},"100523380","mobile-anger-reduction-intervention-100523380","NCT06094933","Mobile Anger Reduction Intervention","A Randomized Controlled Trial of the Mobile Anger Reduction Intervention for Veterans","MARI","Inclusion Criteria:\n\n* Veterans diagnosed with PTSD, established via chart review and a score of greater than or equal to 33 on the PTSD Checklist for DSM-5 (PCL-5)\n* Reporting a score of greater than or equal to 12 on the 5-item Dimensions of Anger Reactions Scale\n* Have not had any changes to type or dose of psychiatric medications for 3 months, with no plans to make adjustments in the next 6 months\n* Able to read at least 6th grade level material\n\nExclusion Criteria:\n\n* Currently in a period of active psychosis or mania\n* Exhibit current prominent suicidal or homicidal ideation requiring immediate intervention\n* Have used the MARI application before as part of another research study\n* Receiving (or plan to receive) other anger management psychotherapy or trauma-focused therapy for PTSD (i.e., prolonged exposure, cognitive processing therapy during the course of the study",{"count":212,"type":19},150,[22],"Difficulty controlling anger is the most commonly reported reintegration concern among combat Veterans, especially those with a diagnosis of posttraumatic stress disorder (PTSD). Problematic anger is associated with significant functional impairment. In the current project, the investigators will compare the Mobile Anger Reduction Intervention (MARI) with a health education mobile intervention (HED) among Veterans with PTSD and problematic anger. Participants will be randomized to the MARI or HED condition. The hypothesis is that participants in the MARI condition will experience greater anger reductions and functional improvements relative to the HED condition.",[181,28],[217,155,218,219],"posttraumatic stress disorder","hostile interpretation bias","mHealth","2025-10-15",{"date":222,"type":39},"2025-10-20",{"date":224,"type":39},"2024-11-12",{"date":226,"type":19},"2028-03-31",{"name":134,"class":135},{"id":229,"slug":230,"hasResults":11,"nctId":231,"briefTitle":232,"officialTitle":233,"acronym":234,"eligibilityCriteria":235,"healthyVolunteers":113,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":236,"targetDuration":4,"studyType":20,"phases":238,"briefSummary":239,"conditions":240,"keywords":246,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":250,"lastUpdatePostDateStruct":251,"startDateStruct":253,"completionDateStruct":255,"leadSponsor":257,"locationsCount":47},"100551077","building-emotional-awareness-and-mental-health-beam-2024-2027-100551077","NCT06455397","Building Emotional Awareness and Mental Health (BEAM) 2024-2027","Implementing BEAM: An mHealth Tool to Prevent Mental Health Problems and Improve Developmental Outcomes in Young Children","BEAM","Inclusion Criteria:\n\n1. Moderate to severe symptoms of depression, anxiety, parenting stress, and\u002For anger (as measured by the PHQ-9, GAD-7, PSI, and PROMIS-Anger). Those who do not have moderate to severe symptoms will meet with a member of the program research team to determine eligibility. This eligibility decision will be based on clinical judgement, ensuring that those with need can participate.\n2. Being a parent or primary caregiver of any gender to an 24- to 71-month-old (i.e., 2-5 year old) child.\n3. Living in Manitoba.\n4. Able to participate in check ins (15 to 60 minutes) via Zoom, phone, direct messaging with a parent peer coach.\n5. 18 years or older.\n6. Able to understand\u002Fread\u002Fspeak in English.\n7. Willing to complete four 45-min questionnaires.\n8. At eligibility screening, a question asks if participants have access to an electronic device for viewing videos and participating in Zoom meetings. Participants who do not have access will be asked to contact the research team. The team may be able to accommodate a limited number of participants by providing relevant devices for the duration of the study.\n9. Participants have IP addresses within Manitoba, Canada, as determined by IP address in REDCap at time of eligibility screener questionnaire completion. Participants will be required to securely upload a photo that includes both a valid piece of Manitoba government identification and the participant's face (i.e., a 'selfie').\n\nExclusion Criteria:\n\n1. Living outside of Manitoba.\n2. Being a parent or primary caregiver to a child outside of the ages of 24- to 71-months (i.e., 2-5 years).\n3. Previously participated in an earlier BEAM trial.\n4. Parents who report self-harm that required medical attention within the past six months or a suicide attempt within the past year will be ineligible to participate in BEAM unless the participant is engaged in individual therapy that attends to this acute risk level with one of the following professionals for the duration of the BEAM program: psychiatrist, psychologist, social worker, or psychotherapist. The research team will email all prospective participants who are pending eligibility to schedule a phone call. This call will determine whether it is feasible to connect the participant with an individual therapist to manage specific needs before engaging in the BEAM program, and discuss if the BEAM program is the right fit for the participant's present needs.\n\nCo-parents will be permitted to participate in BEAM regardless of current mental health challenges. Therefore, co-parents are only subject to inclusion criterion (3) and criteria (5-9). Instead of meeting inclusion criteria (2), parenting partners must be a \"co-parent (e.g., the child's mom, dad, step-parent) or other primary caregiver (e.g., the child's grandma, cousin, uncle, auntie)\" to the corresponding participant's 24- to 71-month-old (i.e., 2-5 year old) child. Co-parents will not receive the same pre-trial screening as parent participants, and thus will not be subject to exclusion criteria.",{"count":237,"type":19},400,[22],"Children are highly sensitive to adversity during their first five years of life, with exposure to chronic parental mental illness (MI) consistently linked to socio-emotional impairments and mental health problems in children. Children born during the COVID-19 pandemic were exposed to unprecedented level of parental distress, with parental MI reported at three times the pre-pandemic rates. This situation underscored a pressing need for scalable solutions to foster positive mental health and developmental outcomes for a generation of children. In response, the investigators developed the Building Emotional Awareness and Mental Health (BEAM) program, an innovative mobile health (mHealth) solution for parents of young children. Clinical trials to date evaluating BEAM have shown promising results, demonstrating reductions in parent depression, anxiety, and harsh parenting practices. This trial involves an effectiveness-implementation hybrid design with co-primary aims of (1) determining BEAM's effectiveness in improving child mental health and developmental outcomes, and (2) evaluating the implementation of BEAM in the community through metrics such as feasibility, acceptability, and uptake. The secondary aim of this trial is to measure BEAM's effectiveness in improving long-term biopsychosocial family outcomes using administrative data. A final exploratory aim of this trial will measure the cost-utility of delivering BEAM relative to extant health programming.\n\nThis trial will evaluate the effectiveness of implementing the BEAM intervention in the community with a sample of 400 parent participants with a child aged 24-71 months. Study participants will complete 12 weeks of psychoeducation modules in the BEAM app, with access to an online social support forum and check ins with a peer coach. Assessments of parent and child symptoms will occur at pre-test before BEAM begins (T1), immediately after the last week of the BEAM intervention (post-test, T2), 6-month follow-up (T3), and 12-month follow-up (T4).\n\nBeginning in 2025, the trial offers participants the option to invite one parenting partner to join them in the program. A parenting partner is defined as a co-parent (e.g., the child's mother, father, or step-parent) or another primary caregiver (e.g., a grandparent, cousin, uncle, or aunt). Each participant may invite one such individual, hereafter referred to as a \"co-parent.\" Co-parents will have access to the BEAM intervention and all its features, with the exception of peer coaching. Co-parents will be eligible to complete the same outcome measures at the same timepoints as participants. Three differences that will separate co-parents from participants are: (1) co-parents will not be asked to complete the ASQ:2-SE or ASQ-3 secondary outcome measures; (2) co-parents will not have access to peer coaching, and (3) co-parents will not be required to be experiencing moderate to severe symptoms of depression, anxiety, parenting stress, and\u002For anger. (Please see Eligibility \\> Eligibility Criteria for the less restrictive inclusion and exclusion criteria for co-parents.) Co-parents will not be counted toward the trial sample size of n=400, and will not be included in primary analyses. Instead, co-parent data will be used in sub-studies to address exploratory research questions.\n\nThe BEAM program offers a promising solution to addressing elevated parental mental health symptoms, parenting stress, and related child functioning concerns. The present implementation trial aims to extend the groundwork established by an open pilot trial and RCT of the BEAM program, in a next step of testing BEAM's readiness for nationwide scaling.",[241,28,242,243,244,245],"Depression, Anxiety","Parenting","Stress, Psychological","Parent-Child Relations","Child Development",[242,247,26,27,248,249],"Mental health","Psychoeducation","App-based intervention","2025-06-13",{"date":252,"type":39},"2025-06-18",{"date":254,"type":39},"2024-03-11",{"date":256,"type":19},"2027-06",{"name":258,"class":46},"Leslie E. Roos",{"id":260,"slug":261,"hasResults":11,"nctId":262,"briefTitle":263,"officialTitle":264,"acronym":4,"eligibilityCriteria":265,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":266,"targetDuration":4,"studyType":267,"phases":4,"briefSummary":268,"conditions":269,"keywords":272,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":274,"lastUpdatePostDateStruct":275,"startDateStruct":277,"completionDateStruct":279,"leadSponsor":280,"locationsCount":47},"100416441","experiences-of-anger-in-patients-in-primary-health-care-with-symptoms-of-generalized-anxiety-100416441","NCT04702711","Experiences of Anger in Patients in Primary Health Care With Symptoms of Generalized Anxiety","Experiences of Anger in Patients in Primary Health Care With Symptoms of Generalized Anxiety - a Qualitative Study From the Perspective of Patients and Health Care Professionals","Patients with symptoms of generalized anxiety\n\nInclusion Criteria:\n\n* Clinically significant level of symptoms of generalized anxiety which is confirmed by a self-rated diagnose of GAD on the questionnaire GAD-Q-IV (Newman et al., 2002; Moore et al., 2014). The questions of the GAD-Q-IV correspond to the A, B, C and D criteria of GAD in Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).\n* Sufficient knowledge in Swedish to be able to answer questionnaires and take part in an interview.\n* If the patient receives any medical or psychological treatment for generalized anxiety this should be recently started and\u002For not yet have led to any notable decrease of symptoms. In the case of pharmacological treatment this should not be associated with more extensive psychological side-effects.\n\nExclusion Criteria:\n\n* Severe psychiatric difficulties where the patient needs specialized psychiatric care\n* Known brain-injury or symptoms of dementia\n* The patient is in an acute crisis\n* Obvious alcohol or substance abuse\n\nHealth care professionals\n\nInclusion Criteria:\n\n* Have a health care profession and work at a primary health care center.\n* Current working experience of at least one year at a primary health care center which included contact with patients with symptoms of generalized anxiety\n\nExclusion Criteria:\n\n\\- Being at the primary health care center in the role of an external student",{"count":175,"type":19},"OBSERVATIONAL","Symptoms of generalized anxiety is common in the general population and is often treated in primary health care. Anger is an emotion that can lead to interpersonal problems but can also be an agent for justice and change. Previous research has shown a link between generalized anxiety and anger but there is a lack of qualitative research investigating how individuals with symptoms of generalized anxiety experience anger.\n\nThe aim of this research study is to increase knowledge about how anger is experienced in adult patients in primary health care with symptoms of generalized anxiety and about the experiences of health care professionals working with patients with symptoms of generalized anxiety.",[270,28,271],"Generalized Anxiety","Primary Health Care",[270,273,28,271],"Worry","2025-04-11",{"date":276,"type":39},"2025-04-16",{"date":278,"type":39},"2020-10-19",{"date":43,"type":19},{"name":281,"class":282},"Kronoberg County Council","OTHER_GOV",{"id":284,"slug":285,"hasResults":11,"nctId":286,"briefTitle":287,"officialTitle":288,"acronym":4,"eligibilityCriteria":289,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":290,"targetDuration":4,"studyType":20,"phases":292,"briefSummary":293,"conditions":294,"keywords":298,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":303,"lastUpdatePostDateStruct":304,"startDateStruct":306,"completionDateStruct":308,"leadSponsor":310,"locationsCount":4},"100576465","the-efficacy-of-lavender-herbal-tea-in-misophonia-100576465","NCT06785649","The Efficacy of Lavender Herbal Tea in Misophonia","The Effect of Lavender Herbal Tea on the Mental Health of Individuals With Misophonia: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Reporting at least three trigger sounds\n* Assessed by a specialist psychiatric nurse and a psychiatrist as humophonia based on the diagnostic criteria for humophonia established by Schröder et al. (2013)\n* Individuals aged 18 and over\n\nExclusion Criteria:\n\n* Allergy to any herbal tea, food or medicine\n* Psychiatric illness or chronic illness\n* Taking psychiatric medication (such as anxiolytics, and antidepressants)\n* Regular use of medication (such as antihypertensive, antidiabetic)\n* Regular use of herbal teas or complementary medicines\n* Tinnitus and\u002For hyperacusis",{"count":291,"type":19},60,[22],"Misophonia is a disorder characterized by a high level of annoyance with certain sounds. Exposure to these sounds causes physical symptoms characterized by anger, aggression, helplessness, overwhelm, and stimulation of the sympathetic nervous system. These emotional and physical reactions can lead to a decline in family relationships, work and school productivity, withdrawal from social relationships, and even suicide. There is limited empirical evidence evaluating the efficacy of therapeutic approaches to misophonia. This limited empirical evidence consists of pharmacological agents such as selective serotonin reuptake inhibitors, stimulants, antipsychotics, and β-Blockers, as well as cognitive behavioral therapy, acceptance and commitment therapy, and dialectical behavior therapy. Complementary therapies are important because of their potential efficacy, tolerability, possible non-interference, and low cost. The fact that lavender has anxiolytic, antidepressant, neuroprotective, and anti-inflammatory properties may affect the emotional and physical responses elicited by misophonia. Therefore, within the scope of the study, misophonia individuals will be divided into two groups; one group will use lavender tea for 14 days and the other group will form a waiting list. The study data will be collected by 'Information Collection Form', 'Misophonia Scale', 'Beck Depression Inventory-II', 'Anxiety Rating Scale', and 'Trait Anger Scale'. SPSS 25.0 software will be used to analyze the data obtained from the research. Considering the limitations of therapeutic approaches for misophonia, testing the effectiveness of lavender in reducing misophonia symptoms will make an important contribution to the literature.",[295,296,27,26,28,297],"Misophonia","Misophonia Treatment","Complementary Medicine",[299,300,301,155,302],"misophonia","anxiety","depression","lavender","2025-01-19",{"date":305,"type":39},"2025-01-21",{"date":307,"type":19},"2025-02-01",{"date":309,"type":19},"2025-02-28",{"name":311,"class":46},"Sakarya University",{"id":313,"slug":314,"hasResults":11,"nctId":315,"briefTitle":316,"officialTitle":317,"acronym":4,"eligibilityCriteria":318,"healthyVolunteers":11,"sex":15,"minAge":144,"maxAge":82,"enrollmentInfo":319,"targetDuration":4,"studyType":20,"phases":321,"briefSummary":322,"conditions":323,"keywords":324,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":329,"startDateStruct":331,"completionDateStruct":332,"leadSponsor":334,"locationsCount":4},"100559105","pilot-study-of-cognitive-behavior-therapy-with-role-plays-in-virtual-reality-for-children-with-behavior-problems-100559105","NCT06559800","Pilot Study of Cognitive Behavior Therapy With Role-plays in Virtual Reality for Children With Behavior Problems","Step by Step - Pilot Study of Cognitive Behavior Therapy With Role-plays in Virtual Reality for Children With Anger, Oppositional or Aggressive Behaviors","Inclusion Criteria:\n\n* Child\u002Fyouth aged between 10-16 years with increased levels of anger or disruptive behaviors,\n* The child's behavior problems is elevated on questions targeting behavioral problems (SDQ conduct problems subscale).\n\nExclusion Criteria:\n\n* Child\u002Fyouth is below 10 years or above 16 years of age\n* No increased levels of anger or disruptive behaviors\n* Child\u002Fyouth is diagnosed with autism, serious depression, psychosis, eating disorder, or self-harm behaviors\n* Child\u002Fyouth has epilepsy or migraine",{"count":320,"type":19},10,[22],"The main aim of this small pilot trial is to evaluate preliminary effects and feasibility of the child intervention YourSkills for child disruptive behavior (e.g., enhanced anger or aggressive behavior) when evaluated in Sweden for children\u002Fyouth aged 10-16 years. YourSkills is based on cognitive behavioral therapy (CBT) and includes practicing of skills in virtual reality (VR).\n\nThe main questions the project aims to answer are:\n\n* What are the preliminary effects of the child\u002Fyouth CBT-VR-program?\n* What is the level of child\u002Fyouth engagement in the CBT-VR program?\n* What are the experiences of parents, children\u002Fyouth and therapists of the program?\n\nThe CBT-VR program is delivered at clinics during ten individual sessions. Parents will answer quantitative measurements before and after treatment, children will answer quantitative measurements before, during and after treatment. Within- group analyses will be conducted to examine experiences and preliminary effects of the program. Parents, children and clinicians are also asked to participate in a qualitative interview after the program has ended.",[88,89,90,91,92,28],[325,326,94,327],"Disruptive behavior","Child behavior problems","Virtual reality","2024-08-15",{"date":330,"type":39},"2024-08-19",{"date":330,"type":19},{"date":333,"type":19},"2024-11-30",{"name":105,"class":46}]