[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"motor-activity\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:motor-activity":34},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,48,80,112,146,167,200,224,249,280,304],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100627815","cranberry-polyphenols-and-stress-resilience-during-multitasking-in-healthy-adults-100627815",false,"NCT07453537","Cranberry Polyphenols and Stress Resilience During Multitasking in Healthy Adults","Cranberry Polyphenols and Human Stress Resilience: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial Integrating Cognitive, Physiological, and Microbiome Adaptations Underlying Nutritional Neuroprotection and Multitasking Performance in Healthy Adults.","CRAN-MULTI","Inclusion Criteria:\n\n* At least 110 pounds\n* Between 30 and 55 years\n* BMI between 18.9 and 29.9 kg\u002Fm²\n* A minimum education level of high school or above\n\nExclusion Criteria:\n\n* Heavy caffeine users (consuming more than 300 mg\u002Fday or more than two cups of coffee per day)\n* Alcohol consumption exceeding three drinks per week\n* A smoking history of 10 years or more, or current use of cannabis products\n* Uncontrolled hypertension\n* Clinically diagnosed illnesses such as diabetes, cardiovascular disease, neurological disorders, or mental health conditions\n* Participants currently taking prescribed anti-inflammatory medications, antibiotics, or antidepressants that may affect study outcomes, particularly those related to blood and fecal sample analysis\n* Individuals who regularly take vitamin or mineral supplements and are unwilling to discontinue them for the duration of the study will not qualify.\n* Participants must be willing to maintain their current daily routine and lifestyle, undergo body weight and height measurements, and notify study coordinators of any illnesses or significant adverse life events during the study period\n* Those with specific dietary restrictions that prevent them from consuming the standardized breakfast sandwich required in the study protocol\n* Participants must successfully complete the on-site multitasking task as a screening measure prior to signing consent.\n* Beck's Depression Inventory score of 21 or higher\n* Beck's Anxiety Inventory score of 21 or higher\n* A history of severe suicidal tendencies, or seasonal depression\n* Pregnancy and breastfeeding (Female participants must complete four pregnancy tests throughout the study and track their menstrual cycle. Those unwilling to comply with these requirements will not be eligible.)\n* Potential participants must not have taken any anti-inflammatory medications, antibiotics, or antidepressants within the past three months prior to the start of the study\n* Individuals who were previously enrolled in IRB#202300950 will be excluded due to the learning effect of cognitive tests, ensuring accurate data collection for this study",true,"ALL","30 Years","55 Years",{"count":22,"type":23},84,"ESTIMATED","INTERVENTIONAL",[26],"NA","This randomized, double-blind, placebo-controlled clinical trial evaluates whether 70 days of daily cranberry juice consumption improves cognitive performance and motor accuracy and reduces psychological and physiological stress responses during a motor-cognitive dual-task multitasking challenge in healthy adults aged 30-55 (Aim 1). It is hypothesized that chronic cranberry juice intake will enhance dual-task performance and attenuate stress reactivity (Hypothesis 1). It is further hypothesized that cranberry juice will mitigate multitasking-related fatigue, mood fluctuations, and cognitive impairment, accompanied by favorable changes in circulating stress biomarkers and stress-regulatory neurochemical pathways (Aim 2\u002FHypothesis 2). Finally, the study incorporates gut analysis to determine whether cranberry juice induces beneficial shifts in the gut microbiota and microbial metabolites (e.g., SCFAs) and whether these changes are associated with improved cognitive and stress-related outcomes, consistent with a microbiome-gut-brain axis mechanism (Aim 3\u002FHypothesis 3).",[29,30,31,32,33,34],"Stress Response","Mental Stress","Multitasking Behavior and Multitasking Ability","Physiological Stress","Cognitive Symptoms","Motor Activity","RECRUITING","2026-06-29",{"date":38,"type":39},"2026-06-30","ACTUAL",{"date":41,"type":23},"2026-08-01",{"date":43,"type":23},"2029-08-01",{"name":45,"class":46},"University of Florida","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":17,"sex":18,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":24,"phases":60,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":47},"100645211","app-based-motor-skills-intervention-in-primary-school-and-home-settings-100645211","NCT07679633","App-based Motor Skills Intervention in Primary School and Home Settings","DigiKids C-RCT: App-based Motor Skills Intervention in Primary School and Home Settings","DigiKids RCT","Inclusion Criteria:\n\n* Children enrolled in the first grade of primary school\n* Sufficient Finnish language proficiency\n* Written informed consent from the guardian and written assent from the child\n\nExclusion Criteria:\n\n* Age under 6 or over 8 years\n* Medical or physical conditions preventing participation in the assessments (including severe musculoskeletal complaints or concussions within the preceding 3 months)\n* Refusal to participate in baseline assessments","6 Years","8 Years",{"count":59,"type":23},314,[26],"The objective of this trial is to evaluate the effectiveness of a mobile app-based motor skills intervention (DigiKids RCT) on motor competence, physical activity, and perceived motor competence compared with standard school practices in primary school children. In addition, the study will examine other factors such as child-specific and family-related factors that might influence the findings.",[63,34],"Healthy",[65,66,67,68,69],"Physical Activity","Mobile Applications","Child","Behavior","Motor Skills","NOT_YET_RECRUITING","2026-06-28",{"date":73,"type":39},"2026-07-01",{"date":75,"type":23},"2026-08-10",{"date":77,"type":23},"2027-05-31",{"name":79,"class":46},"Tampere University",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":17,"sex":18,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":24,"phases":92,"briefSummary":93,"conditions":94,"keywords":96,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":47},"100554348","rtms-to-improve-motor-function-in-autism-100554348","NCT06497920","rTMS to Improve Motor Function in Autism","Modulating Plasticity in the Motor Cortex Using Repetitive Transcranial Magnetic Stimulation to Improve Motor Function in Autism Spectrum Disorder","(AMBLE Autism)","Inclusion Criteria:\n\nASD or control participants must meet all of the inclusion criteria to eligible for this study:\n\n1. Aged between 18 and 40 years old. 40 years is chosen as the cut-off because of the report of high rates of Parkinsonism in autistic adults \\> 39years;\n2. Have IQ\\>70;\n3. Are able to read, write and communicate effectively in English;\n4. Are able to provide informed consent. We will recruit only intellectually-able autistic adults. The intellectual ability will be determined using WASI-II. The ability to provide consent will be determined using clinical assessment.\n5. Have no prior history of seizure;\n6. Must sign and date the informed consent form;\n7. Stated willingness to comply with all study procedures;\n8. Agreement to adhere to Lifestyle Considerations, that is: refrain from consumption of alcohol, tobacco, marijuana, or caffeine on the day of study visits.\n\nAll ASD participants:\n\n1. Will have DSM-5 diagnosis of ASD without intellectual disability, confirmed by clinical assessment and the Autism Diagnostic Observation Schedule - 2 (ADOS-2);\n2. Will have significant motor function difficulties defined as a standard composite score \\\u003C40 (i.e., \\>1 standard deviation below the mean) on either fine or gross motor composite scores of the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition or BOT-2;\n3. Are clinically stable as determined by clinical assessment, with no medication changes over the past 4 weeks. Given the high variability of handedness in ASD, we will include participants with left, right or mixed handedness.\n\nExclusion Criteria:\n\nASD or control participants will be excluded if they experience\u002Fhave:\n\n1. Current pregnancy;\n2. Current or past history of co-morbid medical condition that may require urgent medical intervention;\n3. DSM-5 substance use disorder (other than tobacco) within the past 6 months; however, all participants will be asked to refrain from smoking or taking caffeine four hours prior to the iTBS session;\n4. Significant hearing or visual impairment interfering with the ability to read or hear instructions;\n5. Significantly debilitating medical or neurologic illness (e.g., encephalitis, aneurysms, tumors, central nervous system infections), or acute or unstable medical illnesses as determined by project physician (e.g., uncontrolled diabetes);\n6. Metal implants or a pace-maker;\n7. Prior rTMS treatment;\n\nIn addition, ASD participants will be excluded if they report taking benzodiazepines or anticonvulsants currently.\n\nNT controls will be excluded if they have:\n\n1. Presence of psychopathology other than specific phobia, as screened by Personality Assessment Inventory and;\n2. A known diagnosis of Pervasive Developmental Disorder or ASD among any biologically related family members.","18 Years","40 Years",{"count":91,"type":23},150,[26],"In the current project, investigators have two main goals: i) Testing whether an excessive plasticity, i.e. hyperplasticity in the motor cortex underlies motor function difficulties in autistic adults, and ii) Using repetitive Transcranial Magnetic Stimulation (rTMS) with autistic adults to examine whether resulting reduced hyperplasticity in the motor cortex will be associated with clinical improvements in the motor function.",[95,34],"Autism Spectrum Disorder",[97,98,99,100,101,102],"Autism","Motor Function","Repetitive Transcranial Magnetic Stimulation","Transcranial Magnetic Stimulation","Motor Cortex","Electroencephalography","2026-06-11",{"date":105,"type":39},"2026-06-15",{"date":107,"type":39},"2024-04-24",{"date":109,"type":23},"2029-06-30",{"name":111,"class":46},"Centre for Addiction and Mental Health",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":118,"eligibilityCriteria":119,"healthyVolunteers":17,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":120,"targetDuration":4,"studyType":24,"phases":122,"briefSummary":123,"conditions":124,"keywords":130,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":145},"100643238","aconselha--movimento-protocol-for-online-training-on-physical-activity-and-sedentary-behavior-counseling-100643238","NCT07636291","Aconselha + Movimento: Protocol for Online Training on Physical Activity and Sedentary Behavior Counseling","Development, Implementation, and Effectiveness Evaluation of a Training Program for Health Workers on Physical Activity and Sedentary Behavior: Protocol of Aconselha + Movimento","ACONSELHA+","Inclusion Criteria:\n\n* Healthcare professionals working in Primary Health Care Units (UBS) in Florianópolis (SC), Rio Claro (SP), or São José dos Pinhais (PR) during the data collection period\n* Professionals who are actively working in their positions at the time of recruitment\n* Professionals who voluntarily agree to participate and provide informed consent\n\nExclusion Criteria:\n\n* Professionals who are not actively working during the data collection period\n* Professionals who do not provide informed consent\n* Professionals with incomplete baseline assessment data",{"count":121,"type":23},3306,[26],"This study aims to develop, implement, and evaluate the effectiveness of an online training program on physical activity and sedentary behavior counseling for primary health care workers. The training program is designed to improve competencies related to physical activity and sedentary behavior counseling within primary health care settings. Health professionals working in primary health care units from selected municipalities in Brazil will be invited to participate. Outcomes related to counseling competencies and professional practices will be assessed before and after participation in the training program.",[125,126,127,34,128,129],"Counseling","Exercise","Competence","Primary Health Care Providers","Primary Health Care",[131,132,126,133,134,135],"counseling","Motor activity","Health Centers","Public Health","Primary health care","2026-06-03",{"date":138,"type":39},"2026-06-09",{"date":140,"type":39},"2026-03-11",{"date":142,"type":23},"2026-12-15",{"name":144,"class":46},"Universidade Federal do Paraná",3,{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":150,"acronym":4,"eligibilityCriteria":151,"healthyVolunteers":17,"sex":18,"minAge":88,"maxAge":152,"enrollmentInfo":153,"targetDuration":4,"studyType":24,"phases":155,"briefSummary":156,"conditions":157,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":158,"lastUpdatePostDateStruct":159,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":47},"100627380","unilateral-m1-anodal-tdcs-to-enhance-learning-in-a-gross-movement-videogame-task-100627380","NCT07447882","Unilateral M1 Anodal tDCS to Enhance Learning in a Gross Movement Videogame Task","Inclusion Criteria:\n\n* · Healthy adults between the ages 18-45\n\n  * Answer 'no' to questions 2 through 18 on the tDCS checklist as these factors can increase likelihood of adverse events with tDCS (Appendix 1)\n\n    * No neurological damage, disease, or dysfunction (nerve damage, chronic pain disorders, diabetic neuropathy) that affect the upper limbs.\n    * No significant acute or chronic medical, neurologic, or illness in the patient that, in the judgment of the Principal Investigator, could compromise subject safety, limit the ability to complete the study, and\u002For compromise the objectives of the study\n\nExclusion Criteria:\n\n* · Currently prescribed and taking stimulant medication (Adderall, Ritalin, Vyvanse, etc.)\n\n  * Consumption of over-the-counter stimulants such as caffeine or nicotine (coffee, soda, supplements, energy drinks, tobacco products, or other nicotine containing products such as gum, vape pens, etc...) 12 hours prior to entering the lab on the day of testing as this can directly affect cortical excitability. If a subject takes any of these substances 12 hours prior to session 1 they will be asked to reschedule for a later date.\n  * Have played the game Beat Saber on a Virtual Reality Headset in the last 12 months.","45 Years",{"count":154,"type":23},52,[26],"Virtual reality as a gaming method is being used more regularly due to its immersive environments and total body playability. A few studies have used VR paired with brain stimulation as a clinical treatment for PTSD (van't Wout-Frank et al. 2024), as well as for regaining movement and cognitive abilities following stroke (Cheng et al. 2024; Lima et al. 2024). While a clinical use for VR and brain stimulation is the ultimate goal, there have still been no basic science investigations studying the efficacy of pairing the two. This investigation will be the first in exploring the connection between VR and brain stimulation as it relates to behavioral improvements (learning the game quicker) and eventually the investigators will begin to study the exact cortical changes that facilitate the accelerated learning. The game \"Beat Saber\" was chosen because it requires the subjects to move their arm in a large 3-Dimensional space and gives a performance metric after each trial to measure improvement",[34],"2026-05-28",{"date":160,"type":39},"2026-06-01",{"date":162,"type":39},"2025-04-23",{"date":164,"type":23},"2026-08",{"name":166,"class":46},"Indiana University",{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":172,"acronym":173,"eligibilityCriteria":174,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":175,"targetDuration":4,"studyType":177,"phases":4,"briefSummary":178,"conditions":179,"keywords":184,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":196,"leadSponsor":198,"locationsCount":47},"100640793","physical-activity-level-at-home-in-cmt1a-patients-wearable-sensor-assessment-100640793","NCT07591779","Physical Activity Level at Home in CMT1A Patients: Wearable Sensor Assessment","Study of the Relationship Between Clinical and Functional Characteristics of Patients With CMT1A Disease and Their Level of Physical Activity at Home Measured Using Portable Electronic Sensors","CMT1A-HOME","Inclusion Criteria:\n\n1. Age ≥ 18 years\n2. Genetically confirmed diagnosis of CMT1A (PMP22 duplication on chromosomal analysis)\n3. Followed at the National Reference Centre for Rare Peripheral Neuropathies (Service de Neurologie, CHU de Limoges) and\u002For having undergone gait analysis at the Quantified Movement Analysis Laboratory (Laboratoire d'AQM), Service de Médecine Physique et de Réadaptation, CHU de Limoges\n4. Ability to walk independently (with or without walking aids)\n5. Informed consent obtained\n6. Affiliated to French social security system\n\nExclusion Criteria:\n\n1. Other associated neurological condition that could independently affect walking or motor activity\n2. Inability to wear the sensor device (skin allergy, sensory intolerance)\n3. Inability to comply with study procedures (cognitive impairment, no fixed domicile)\n4. Participation in another interventional study during the same period\n5. Pregnant or breastfeeding women\n6. Patients under legal protection (guardianship or curatorship)",{"count":176,"type":23},60,"OBSERVATIONAL","Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common hereditary peripheral neuropathy, affecting approximately 26,000 patients in France. It presents as chronic and progressive sensorimotor deficits predominantly affecting the distal lower limbs, with onset typically in childhood. There is currently no specific pharmacological treatment; management remains symptomatic.\n\nThis research will:\n\nIn the long run, validated wearable sensors could improve patient follow-up, personalize rehabilitation, and support the design of clinical trials for CMT1A - including trials of the novel \"Nano-Cur\" treatment currently under development.",[180,181,34,182,183],"Charcot-Marie-Tooth Disease, Type IA","Peripheral Neuropathy Hereditary","Walking, Difficulty","Neuromuscular Diseases",[185,186,187,188,189,190,191],"CMT1A","wearable sensor","actigraphy","physical activity","CMT-FOM","functional assessment","peripheral neuropathy","2026-05-20",{"date":194,"type":39},"2026-05-22",{"date":160,"type":23},{"date":197,"type":23},"2027-06-30",{"name":199,"class":46},"University Hospital, Limoges",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":204,"acronym":4,"eligibilityCriteria":205,"healthyVolunteers":11,"sex":18,"minAge":206,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":24,"phases":209,"briefSummary":210,"conditions":211,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":215,"lastUpdatePostDateStruct":216,"startDateStruct":218,"completionDateStruct":220,"leadSponsor":222,"locationsCount":47},"100638334","quantitative-monitoring-of-disability-care-quality-for-long-term-care-facilities-2-100638334","NCT07579832","Quantitative Monitoring of Disability Care Quality for Long-Term Care Facilities 2","Inclusion Criteria:\n\n* Older adults with disabilities:\n\n  * Aged ≥ 65 years.\n  * Classified as CMS level 2-6 under Taiwan Long-Term Care Need Assessment.\n  * Currently receiving at least one Long-Term Care 2.0 service (e.g., home care, home-based rehabilitation, or respite care).\n  * Have normal cognitive function, or a Mini-Mental State Examination (MMSE) score ≥ 23 when cognitive screening is performed.\n  * Own and are able to use a smartphone.\n  * Willing to participate and provide written informed consent.\n* Family caregivers:\n\n  * Have normal cognitive function, or a Mini-Mental State Examination (MMSE) score ≥ 23 when cognitive screening is performed.\n  * Own and are able to use a smartphone.\n  * Willing to participate and provide written informed consent.\n* Multidisciplinary rehabilitation professionals:\n\n  * Employed or contracted by a home-based long-term care institution with at least three professional disciplines (e.g., physical therapists, occupational therapists, nurses, social workers).\n  * Own and are able to use a smartphone.\n  * Willing to participate and provide written informed consent.\n\nExclusion Criteria:\n\n* Older adults with disabilities:\n\n  * Severe acute medical conditions or unstable physiological status.\n  * Severe cognitive impairment without a caregiver capable of assisting with questionnaires.\n  * Not currently receiving any long-term care services.\n* Family caregivers:\n\n  * Severe acute medical conditions or unstable physiological status.\n  * Severe cognitive impairment without ability to complete questionnaires.\n  * Not currently involved in long-term care services.\n* Multidisciplinary rehabilitation professionals:\n\n  * Providing services exclusively in non-home-based settings (e.g., institutional or hospital-only care).","65 Years",{"count":208,"type":23},1080,[26],"The goal of this clinical trial is to evaluate whether a smart wearable wristband-based care system can improve the quality of care and physical activity levels among older adults with disabilities receiving home-based care. The study population includes older adults with disabilities, their family caregivers, and multidisciplinary rehabilitation service providers.\n\nThe main questions it aims to answer are:\n\n1. Whether the use of a smart wearable wristband can improve functional performance, as measured by Activities of Daily Living (ADLs), Instrumental Activities of Daily Living (IADLs), and Integrated Care for Older People (ICOPE) assessments?\n2. Whether the intervention can increase physical activity levels and improve overall care quality, while reducing caregiver burden and enhancing satisfaction?\n\nParticipants will:\n\n1. Wear a smart wearable wristband continuously for 8 weeks to record physical activity data, including step count, activity level, heart rate, and fatigue index.\n2. Undergo assessments at baseline and after the 8-week intervention, including Activities of Daily Living (ADLs), Instrumental Activities of Daily Living (IADLs), Integrated Care for Older People (ICOPE), and the Chinese Version of the Physical Activity Scale for the Elderly (PASE-C).\n3. Provide data on caregiver stress, satisfaction, and service utilization for the analysis of care quality.",[212,213,214,34],"Disabled Persons","Activities of Daily Living","Aged","2026-05-06",{"date":217,"type":39},"2026-05-12",{"date":219,"type":23},"2026-05-15",{"date":221,"type":23},"2027-12-31",{"name":223,"class":46},"National Health Research Institutes, Taiwan",{"id":225,"slug":226,"hasResults":11,"nctId":227,"briefTitle":228,"officialTitle":229,"acronym":230,"eligibilityCriteria":231,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":232,"targetDuration":4,"studyType":177,"phases":4,"briefSummary":234,"conditions":235,"keywords":236,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":239,"lastUpdatePostDateStruct":240,"startDateStruct":242,"completionDateStruct":244,"leadSponsor":246,"locationsCount":47},"100621669","physical-activity-trends-in-cancer-survivors-treated-at-the-movement-and-rehabilitation-clinic-100621669","NCT07373626","Physical Activity Trends in Cancer Survivors Treated at the 'MOvement and REhabilitation' Clinic","Prospective Study on Physical Activity Trends in Cancer Survivors Treated at the 'MOvement and REhabilitation' (MO.RE) Clinic","MOREACTIVE2025","Inclusion Criteria:\n\n* Diagnosis of cancer\n* Age over 18 years\n* Signed informed consent\n* Patients for whom a physical exercise program can be proposed\n\nExclusion Criteria:\n\n* Patients for whom the physiatric assessment identifies a need for individual rehabilitative treatment\n* Significant language barrier\n* Neuropsychological, psychiatric, or cognitive deficits, or clinical conditions that prevent participation in an independent physical activity program",{"count":233,"type":23},50,"An active lifestyle after a cancer diagnosis can reduce the side effects of treatment and improve quality of life, mental health, and survival. Recent evidence in the literature confirms its benefits across various types and stages of cancer. However, the majority of cancer patients do not reach the recommended levels of physical activity due to physical, psychological, and logistical barriers. It is essential that healthcare professionals provide motivational support and address individual barriers to physical activity through the active involvement of patients, thus promoting the adoption and maintenance of an active lifestyle. To achieve this, personalization of physical activity programs is crucial. For this reason, the MOvement \\& REhabilitation clinic was established in 2022, where a dedicated physiotherapist provides personalized consultations and educational support to promote physical activity among cancer patients.\n\nThis study aims to evaluate the trend over time in the amount of physical activity among cancer patients attending the \"MOvement and REhabilitation\" (MO.RE) clinic. The study also seeks to assess patient engagement, the amount of resources used to help patients maintain an active lifestyle, and any barriers to physical activity.",[68,34],[65,237,238],"Physical Exercise","Onco-hematological patients","2026-01-23",{"date":241,"type":39},"2026-01-28",{"date":243,"type":39},"2025-09-01",{"date":245,"type":23},"2027-02-28",{"name":247,"class":248},"Azienda USL Reggio Emilia - IRCCS","OTHER_GOV",{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":255,"eligibilityCriteria":256,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":257,"targetDuration":4,"studyType":177,"phases":4,"briefSummary":258,"conditions":259,"keywords":264,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":271,"lastUpdatePostDateStruct":272,"startDateStruct":274,"completionDateStruct":276,"leadSponsor":278,"locationsCount":47},"100592913","physical-activity-in-cancer-patients-in-an-oncology-day-clinic---implementing-a-person-centered-program-led-by-nurses-100592913","NCT06999616","Physical Activity in Cancer Patients in an Oncology Day Clinic - Implementing a Person-centered Program Led by Nurses","Promoting Physical Activity in Individuals With Cancer in an Oncology Day Clinic - Testing the Feasibility of the Implementation of a Physical Activity Concept Within an Interprofessional Team Led by Nurses OnkoMoveNurse - Proof of Concept","OnkoMoveNurse","Inclusion Criteria:\n\n1. diagnosis of cancer,\n2. at least three treatments at the oncology outpatient clinic in Münsterlingen during the study period,\n3. aged ≥18 years, and\n4. sufficient knowledge of German.\n\nExclusion Criteria:\n\n* pregnancy",{"count":233,"type":23},"Background: Physical activity has demonstrated benefits in alleviating side effects and improving well-being in people with cancer. However, activity levels remain low during systemic treatment. Nurses are optimally positioned to lead interventions fostering an activity-friendly culture.\n\nObjective: This study aims to evaluate the feasibility and potential effects of the nurse-led, interprofessionally developed physical activity concept OncoMoveNurse in an outpatient oncology setting.\n\nMethods: Using a mixed-methods design over 15 months (10\u002F2024-12\u002F2025), the study includes implementation and evaluation phases. Quantitative data (n=50 patients, collected from 06\u002F2025-09\u002F2025) will assess primary (physical activity behavior) and secondary outcomes (self-efficacy, well-being, mood) via validated PROMs. Qualitative insights will be gathered through digital storytelling (n=2 patients, n=2 nurses) and one focus group (n=8 interprofessional team members). Inclusion criteria for patients include age ≥18, cancer diagnosis, at least three treatments in the day clinic, and sufficient German language skills.\n\nIntervention: OncoMoveNurse comprises five adaptable components: modular activity structure, safety framework, communication strategy, a team approach, and person-centered orientation. Supporting materials (e.g., posters, videos, exercise tools) and tailored implementation strategies were co-developed in alignment with core values.\n\nAnalysis: Quantitative data will be analyzed using SPSS (paired t-tests, p\\\u003C.05); qualitative data via content analysis in MAXQDA. A mixed-methods synthesis will integrate findings.\n\nEthics \\& Data Protection: Patient data collection will commence following ethics approval. All data are anonymized, stored securely, and handled in accordance with Swiss data protection laws.\n\nConclusion: This study will provide insights into the feasibility of nurse-led physical activity promotion in outpatient oncology and inform future outcome evaluations.",[260,34,261,262,263],"Neoplasms","Chemotherapy","Antitumor Drugs","Activity Level",[265,266,267,268,269,270,188],"activity promotions","proof-of-concept","implementation","activity concept","excercise","cancer patient","2025-12-03",{"date":273,"type":39},"2025-12-10",{"date":275,"type":39},"2025-08-01",{"date":277,"type":23},"2026-08-31",{"name":279,"class":46},"St.Gallen University of Applied Sciences",{"id":281,"slug":282,"hasResults":11,"nctId":283,"briefTitle":284,"officialTitle":285,"acronym":4,"eligibilityCriteria":286,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":287,"targetDuration":4,"studyType":24,"phases":289,"briefSummary":290,"conditions":291,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":295,"lastUpdatePostDateStruct":296,"startDateStruct":298,"completionDateStruct":300,"leadSponsor":302,"locationsCount":47},"100553218","implementation-of-ivs3-for-upper-limb-motor-recovery-100553218","NCT06483230","Implementation of IVS3 for Upper Limb Motor Recovery","A Pilot Study on Tolerance and Ease of Implementation of Intensive Visual Stimulation (IVS3) in Daily Practice for Upper Limb Motor Recovery in Outpatient Rehab Center","Inclusion Criteria:\n\n1. Age ≥ 18 years old\n2. English speaking\n3. History of ischemic or hemorrhagic stroke ≥ 6 months prior to study enrolment\n4. FMA-UE: 20 \\\u003C x \\\u003C 50 (moderate impairments)\n5. With or without hemi spatial neglect\n\nExclusion Criteria:\n\n1. Spasticity or increased tone with MAS ≥3 in the upper extremity\n2. Unable to communicate effectively or provide informed consent\n3. Significant visual impairments\n4. Concurrent occupational therapy being received outside of the study\n5. Pregnant or incarcerated individuals",{"count":288,"type":23},25,[26],"This study measures participant satisfaction and upper extremity function in outpatients with chronic stroke when exposed to the IVS3 device. Investigators hypothesize that treatment with the IVS3 device will be feasible and tolerable for use in the outpatient setting.",[292,293,294,34],"Neglect, Hemispatial","Stroke, Cardiovascular","Mirror Movement","2025-10-27",{"date":297,"type":39},"2025-10-29",{"date":299,"type":39},"2024-10-02",{"date":301,"type":23},"2027-06",{"name":303,"class":46},"Weill Medical College of Cornell University",{"id":305,"slug":306,"hasResults":11,"nctId":307,"briefTitle":308,"officialTitle":309,"acronym":4,"eligibilityCriteria":310,"healthyVolunteers":17,"sex":18,"minAge":311,"maxAge":4,"enrollmentInfo":312,"targetDuration":4,"studyType":24,"phases":313,"briefSummary":314,"conditions":315,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":317,"lastUpdatePostDateStruct":318,"startDateStruct":320,"completionDateStruct":322,"leadSponsor":324,"locationsCount":47},"100490688","a-good-start-matters-intervention-study-100490688","NCT05669378","A Good Start Matters Intervention Study","A Good Start Matters: Do Supportive Childcare Centre Environments, Policies and Practices Enhance Physical Activity?","Inclusion Criteria for childcare center:\n\n* Located in the Metro Vancouver region\n* Provides care to at least 10 children older than 2 1\u002F2 years and younger than 6 years\n* Childcare program that is longer than 4 hours each day\n\nInclusion for child outcomes \u002F measurement\n\n* children must attend a childcare that has volunteered to participate in the study\n* Child must be older than 2 1\u002F2 years and younger than 6 years of age\n\nInclusion Criteria for managers and staff childcare centers:\n\n\\- Managers at licensed BC childcare facilities, working full time (at least 3 full days per week) in a facility for children aged 2½ to 6 years, defined as an Executive Director, supervisor, or program manager. Aged 19 years or older.\n\nOR\n\n\\- Childcare staff at licensed BC childcare facilities, working full time (at least 3 full days per week), defined as Early Childhood Educator, instructor, or staff that cares for 2½ to 6-year-old children. Aged 19 years or older.\n\nExclusion Criteria for childcare center:\n\n* Located outside Metro Vancouver region\n* Facilities caring only for children under 2 1\u002F2 years old or older than 6 years\n* Family or in-home multi-age childcare\n\nExclusion Criteria for managers and staff childcare centers:\n\n* Do not care or supervise 2 ½ to 6 years old children\n* Work less than 3 full days per week\n* Administrative assistant\u002Foffice manager\n* Younger than 19 years of age","30 Months",{"count":154,"type":23},[26],"The BC government and partners developed Active Play Standards and a capacity-building strategy to help childcare centers implement the Standards. We have developed an intervention to supplement the governmental capacity-building strategies. The intervention is comprised of implementation support strategies targeted at childcare providers in BC that will aid with the sustainment of Active Play best practices at their facilities. The impact of the intervention will be assessed by measuring its impact on a) change in practices with respect to Active Play; and b) improving child-level outcomes (children's physical activity, sedentary behavior, and motor skill competencies). The findings will inform future policies and enhance our understanding of how policy action supported by communication, capacity-building, and sustainment strategies influence the environment of childcare centres.",[316,34],"Physical Inactivity","2025-04-14",{"date":319,"type":39},"2025-04-16",{"date":321,"type":39},"2023-10-25",{"date":323,"type":23},"2025-09-30",{"name":325,"class":46},"University of British Columbia"]