[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"smartwatches\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:smartwatches":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,91],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":4},"100631070","sustainability-of-the-effects-of-an-adapted-physical-activity-program-on-physical-fitness-and-psycho-behavioral-factors-in-patients-with-chronic-diseases-100631070",false,"NCT07495891","Sustainability of the Effects of an Adapted Physical Activity Program on Physical Fitness and Psycho-behavioral Factors in Patients With Chronic Diseases","Sustainability of the Effects of an Adapted Physical Activity Program on Physical Fitness and Psycho-behavioral Factors in Patients With Chronic Diseases: the Influence of Program Duration and the Use of a Smartwatch","DURATECH-APA","Inclusion Criteria:\n\n* Patients over the age of 18\n* French-speaking patients\n* Patients with a chronic condition diagnosed by a doctor\n* Patients with a doctor's prescription for APA\n* Patients capable of understanding instructions\n* Patients enrolled in the Social Security system\n* Patients referred to Maison Sport Santé La Musse by a doctor for the first time\n\nNon inclusion Criteria :\n\n* Medical contraindications to physical exertion\n* Pregnant women\n* Individuals under legal guardianship, conservatorship, or judicial protection.\n* Severe cognitive or motor impairment\n* Lack of proficiency in French\n* Patients in the acute phase requiring specialized care\n* Patients simultaneously participating in another interventional research study\n* Inability to attend sessions regularly or adhere to the schedule of evaluations.\n* Patients who have already completed a program at the Maison Sport Santé\n\nExclusion Criteria:\n\n* Completion of fewer than 16 APA sessions (less than 70% of sessions)\n* Acute exacerbation of a chronic condition during follow-up\n* For groups without smartwatches, the use of a digital tool such as a physical activity tracker by participants would constitute an exclusion criterion\n* Completion of a patient therapeutic education program","ALL","18 Years",{"count":20,"type":21},280,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to determine the extent to which different approaches to adapted physical activity coaching influence physical fitness, psycho-behavioral, and anthropometric parameters in patients with stabilized chronic conditions who have been referred to a Sport-Health Center by their physician. The trial includes four parallel groups, distinguishing between two program durations (3 months or 6 months) and the use or non-use of a smartwatch as a tool for monitoring activity. All participants complete 24 sessions of adapted physical activity (APA), in accordance with the standard practices of the La Musse Sport-Health Center, where the study is entirely conducted. However, the distribution of sessions differs by group: two sessions per week over three months or one session per week over six months. Randomization is stratified by age, sex, and baseline fitness level. Assessments are conducted at the following five time points: enrollment (T0), end of the 3-month program (T1), end of the 6-month program (T2), followed by follow-up at 12 months (T3) and 18 months (T4), to observe the durability of the effects after the supervised phase. The primary outcome measure is improvement in physical fitness and anthropometric parameters, objectively measured using tests recognized for their reliability (TDM6, Sit-to-Stand 30s, Timed Up and Go, Sit and Reach, grip strength, BMI, waist circumference). The secondary outcomes focus on changes in motivation toward health-related physical activity (EMAPS), perceived self-efficacy to engage in physical activity (ECS), and self-reported physical activity (IPAQ-SF), which will be collected regularly throughout the program, more frequently than in standard care. A total of 280 patients will be enrolled to ensure sufficient statistical power, taking into account an anticipated loss-to-follow-up rate over 18 months. Data collection and processing will be pseudonymized and conducted on the secure network of La Musse Hospital.",[27,28,29,30,31],"Adapted Physical Activity","Smartwatches","Chronic Disease","Motivation for Physical Activity","Physical Fitness",[33,34,35,36,37,38,39,40],"Adapted physical activity","Chronic diseases","Smartwatch","Sustainability of effects","Motivation for physical activity","Self-efficacy in physical activity","Physical fitness","Longitudinal follow-up","NOT_YET_RECRUITING","2026-03-23",{"date":44,"type":45},"2026-03-27","ACTUAL",{"date":47,"type":21},"2026-03-30",{"date":49,"type":21},"2028-12-31",{"name":51,"class":52},"Hopital La Musse","OTHER",{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":61,"minAge":18,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":4,"briefSummary":65,"conditions":66,"keywords":72,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":90},"100605450","step-count-and-treatment-response-in-neoadjuvant-breast-cancer-100605450","NCT07162675","Step Count and Treatment Response in Neoadjuvant Breast Cancer","A Multicenter Prospective Study: The Impact of Step Count Measured by Smartwatches on Treatment Response in Non-Metastatic HER2-Negative Breast Cancer Patients Receiving Neoadjuvant Therapy","NEOBRE-STEP","Inclusion Criteria:\n\n* Female patients aged ≥18 years.\n* Pathologically confirmed non-metastatic HER2-negative breast cancer.\n* Candidates scheduled to receive neoadjuvant systemic therapy followed by surgery.\n* ECOG performance status 0-2.\n* Ability to provide informed consent.\n\nExclusion Criteria:\n\n* Metastatic breast cancer at diagnosis.\n* HER2-positive breast cancer.\n* Previous systemic therapy for current breast cancer.\n* Severe comorbidities limiting mobility or physical activity (e.g., advanced neurologic or musculoskeletal disorders).\n* ECOG performance status ≥3.\n* Pregnancy or breastfeeding.\n* Refusal or inability to use a smartwatch device.","FEMALE",{"count":63,"type":21},82,"OBSERVATIONAL","This prospective multicenter observational study (NEOBRE-STEP) investigates the impact of daily step counts, measured by Huawei Fit 2 smartwatches, on treatment response in patients with non-metastatic Human Epidermal Growth Factor Receptor 2 (HER2)-negative breast cancer undergoing neoadjuvant systemic therapy. Patients will wear smartwatches to continuously record step counts, activity intensity, sleep, and heart rate. Patient-reported outcomes, including sleep quality (Pittsburgh Sleep Quality Index, PSQI) and quality of life (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30, EORTC QLQ-C30), will be assessed at baseline and after treatment. The primary outcomes are pathological complete response (pCR) and Miller-Payne score. Secondary outcomes include sleep quality, quality of life, perioperative outcomes, and feasibility of smartwatch monitoring.",[67,68,69,70,71,28],"Breast Neoplasm Malignant Female","Exercise","Breast Cancer Females","Wearable Technology","Sleep Quality",[73,74,35,75,76,77,78],"neoadjuvant therapy","HER2-Negative Breast Cancer","Step Count","Physical Activity","Patient-Reported Outcomes","Quality of Life (EORTC QLQ-C30)","RECRUITING","2026-02-19",{"date":82,"type":45},"2026-02-20",{"date":84,"type":45},"2025-09-08",{"date":86,"type":21},"2026-08-29",{"name":88,"class":89},"Ankara Etlik City Hospital","OTHER_GOV",2,{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":95,"acronym":96,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":98,"targetDuration":4,"studyType":22,"phases":100,"briefSummary":101,"conditions":102,"keywords":109,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":126},"100571781","diagnosis-of-atrial-fibrillation-in-postoperative-thoracic-surgery-using-a-smartwatch-100571781","NCT06724718","Diagnosis of Atrial Fibrillation in Postoperative Thoracic Surgery Using a Smartwatch","THO-FA-WATCH","Inclusion Criteria:\n\n* Adults (\\>18 years old).\n* Patients undergoing major thoracic surgery with one-lung ventilation within the past 48 hours.\n* Scheduled pneumonectomy or lobectomy.\n* Admission to a conventional surgical unit postoperatively.\n* Ability to perform single-lead ECG using a smartwatch.\n* Coverage under a social security system.\n* Signed informed consent\n\nExclusion Criteria:\n\n* History of atrial fibrillation.\n* Requirement for telemetry for AV block or tachyarrhythmias (\\>140 bpm).\n* Dependency on a pacemaker.\n* Participation in another interventional clinical trial affecting POAF incidence.\n* Mediastinal, pleural, or chest wall surgery.\n* Reoperations or surgeries performed more than 48 hours prior.\n* Pregnant women.\n* Patients under guardians or similar legal protection.",{"count":99,"type":21},302,[24],"Postoperative atrial fibrillation (POAF) occurs in approximately 20% of patients following thoracic surgery. Early diagnosis is essential to prevent complications such as heart failure, stroke, myocardial infarction, and increased mortality. Smartwatches equipped with single-lead ECG capabilities and algorithms to detect asymptomatic atrial fibrillation (AF) offer a potential solution. This study aims to evaluate the effectiveness of smartwatches in detecting POAF compared to standard care.",[103,104,28,105,106,107,108],"Postoperative Atrial Fibrillation","Thoracic Surgery","Rhythm Monitoring","Cardiovascular Prognosis","Asymptomatic Atrial Fibrillation","Randomized Trial",[110,111,112,113,114,115,116],"Postoperative atrial fibrillation","thoracic surgery","smartwatches","rhythm monitoring","cardiovascular prognosis","asymptomatic atrial fibrillation","randomized trial","2025-06-11",{"date":119,"type":45},"2025-06-12",{"date":121,"type":45},"2025-06-01",{"date":123,"type":21},"2027-12",{"name":125,"class":52},"Centre Hospitalier Universitaire, Amiens",1]