[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"meditation-training\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:meditation-training":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,57],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":34,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":56},"100634675","choice-and-autonomy-in-learning-mindfulness-for-pediatric-residents-100634675",false,"NCT07542769","Choice and Autonomy in Learning Mindfulness for Pediatric Residents","CALM-PR","Inclusion Criteria:\n\n* Current categorical pediatrics residents at Northwestern University.\n* Preliminary pediatrics residents who intend to continue in pediatrics.\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n\\- None; all pediatric residents meeting inclusion criteria are eligible.",true,"ALL",{"count":19,"type":20},42,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study is a pilot clinical trial designed to evaluate a flexible, online mindfulness program for pediatric residents. Medical training can be stressful, and although mindfulness programs are often offered to support well-being, many are either in-person or follow a fixed format that may not fit individual schedules or preferences. This study will test a digital mindfulness program called Wakeful, which allows participants to complete the course at their own pace. Participants will be randomly assigned to one of two groups: one group will be able to choose the length of their mindfulness program (3, 5, or 7 weeks), while the other group will be assigned a program length without a choice. The goal is to understand whether giving participants a choice improves how often they use the program, how satisfied they are with it, and whether they complete it. The main outcomes of this study focus on how participants interact with the program, including how many sessions they complete, how often they practice mindfulness on their own, and how useful and relevant they find the program. The study will also look at overall satisfaction and how many participants drop out before finishing. In addition, the study will explore whether participants report changes in mindfulness and compassion for others, although it is not designed to determine clinical improvements in mental health. By understanding how pediatric residents engage with different program formats, this study aims to inform the design of more flexible and user-centered digital wellness programs that better fit into demanding medical training environments.",[26,27,28,29,30,31,32,33],"Program Engagement","Treatment Adherence and Compliance","Mindfulness","Self-Compassion","Physician Burnout","Psychological Well-Being","Meditation","Meditation Training",[28,32,35,36,37,38,39,27,40,26,41,42,29,43],"Digital Health Intervention","Internet-Based Intervention","Physician Well-Being","Graduate Medical Education","Pediatric Residency","Patient Acceptance of Health Care","User Engagement","Pilot Projects","Compassion","RECRUITING","2026-05-21",{"date":47,"type":48},"2026-05-26","ACTUAL",{"date":50,"type":48},"2026-04-13",{"date":52,"type":20},"2027-05-01",{"name":54,"class":55},"Northwestern University","OTHER",1,{"id":58,"slug":59,"hasResults":11,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":4,"eligibilityCriteria":63,"healthyVolunteers":11,"sex":17,"minAge":64,"maxAge":4,"enrollmentInfo":65,"targetDuration":4,"studyType":21,"phases":67,"briefSummary":68,"conditions":69,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":4},"100616852","effect-of-meditation-as-an-adjunct-to-cardiac-rehabilitation-100616852","NCT07310992","Effect of Meditation as an Adjunct to Cardiac Rehabilitation","The Effect of Meditation Practice Combined With Cardiac Rehabilitation on Improving Quality of Life and Controlling Blood Pressure.","Inclusion Criteria:\n\n* Patients of both sexes, aged 18 years or older.\n* Newly enrolled in the Phase II Cardiac Rehabilitation Program.\n* Clinically stable condition with medical clearance to perform aerobic and resistance exercises.\n* Diagnosis of cardiovascular disease (e.g., coronary artery disease, post-myocardial infarction, post-cardiac surgery, or stable heart failure) warranting rehabilitation.\n* Willingness and cognitive ability to provide written informed consent.\n* Availability to attend the twice-weekly sessions for the 12-week duration of the study.\n\nExclusion Criteria:\n\n* Current regular practice of meditation, yoga, or other mind-body techniques (defined as formal practice more than once a week in the previous 3 months).\n* Current participation in other psychological or behavioral intervention clinical trials.\n* Severe cognitive impairment or psychiatric disorders that preclude understanding of the meditation instructions or group participation (e.g., dementia, untreated psychosis).\n* Unstable clinical conditions such as unstable angina, uncontrolled arrhythmias, or decompensated heart failure that contraindicate physical exercise.\n* Significant orthopedic or neurological limitations that prevent the performance of the exercise protocol.\n* Refusal to participate in the randomization process.","18 Years",{"count":66,"type":20},80,[23],"Cardiovascular rehabilitation is a well-established standard of care that significantly reduces morbidity and mortality while improving quality of life. However, integrating behavioral interventions into physical training may offer additional benefits for autonomic regulation and emotional well-being.\n\nThis randomized clinical trial aims to investigate the efficacy of adding a brief, guided mindfulness meditation session to a standard cardiovascular rehabilitation program. The study seeks to determine whether this combined intervention enhances blood pressure control, improves perceived quality of life, and increases patient adherence compared to standard rehabilitation alone.\n\nParticipants newly enrolled in the Cardiac Rehabilitation Service will be randomized into two groups. Both groups will undergo a standard 12-week regimen of aerobic and resistance training combined with optimized medical therapy. The intervention group will additionally receive 15 minutes of voice-guided mindfulness meditation at the end of each exercise session. Key outcome measures include blood pressure variability, quality of life scores (assessed via EQ-5D), and attendance rates.",[70,33,71],"High Blood Pressure (& [Essential Hypertension])","Rehabilitation Exercise","NOT_YET_RECRUITING","2025-12-30",{"date":75,"type":48},"2026-01-05",{"date":77,"type":20},"2026-01-15",{"date":79,"type":20},"2028-01-15",{"name":81,"class":55},"Instituto Dante Pazzanese de Cardiologia"]