[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Amsterdam University of Applied Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":93},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,67],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100625938","plant-based-protein-rich-weight-loss-intervention-in-55-adults-with-obesity-100625938",false,"NCT07429136","Plant-based Protein-rich Weight Loss Intervention in 55+ Adults With Obesity","2EAT","Inclusion Criteria:\n\n* Aged 55 or older\n* Are obese: have a BMI of \\>30 kg\u002Fm2 or BMI \\>27 kg\u002Fm2 and waist circumference \\>88 cm (women) or \\>102 cm (men)\n* Living independently (not in a health facility)\n* The willingness that the general practitioner will be notified of study participation\n* Written informed consent\n* Willingness to comply with the protocol\n* Consent of the study physician\n\nExclusion Criteria:\n\n* Inability to understand the Dutch language\n* Cognitive impairment (MMSE \\\u003C15)\n* Use of total or partial parenteral nutrition (TPN)\n* Alcohol or drug abuse in the opinion of the investigator\n* Current enrolment in a fixed rehabilitation program or other intervention studies\n* Palliative treatment or a life expectancy of ≤ 3 months\n* Following a vegetarian or vegan (100% plant-based) diet\n* Bariatric surgery\n* Active medical treatment interfering with this intervention (e.g. weight loss medication as Ozempic, cancer patients receiving systemic and immune therapy)\n* Physical disabled: unable to meet the general daily exercise guideline for adults\n* Planned a holiday during the intervention period and is unable to attend group- or individual sessions for \\> 3 weeks\n\nThe health conditions below will be assessed by the study physician. When a condition interferes the dietary treatment or if the diet worsens the participants health it counts as exclusion criteria:\n\n* Diagnosed with unstable coronary heart disease (CHD), decompensated heart failure, uncontrolled hypertension or uncontrolled arrhythmias (e.g. heart failure NYHA \\>3)\n* Diagnosed degenerative neurocognitive disorders\n* Diagnosed with renal failure\n* COPD GOLD \\>3","ALL","55 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of the 2EAT RCT is to investigate whether a shift towards more plant-based (≥60% with a minimum of 50%) protein intake can be achieved in an energy restricted diet for three and six months in older adults (55+) with obesity.\n\nThe 2EAT researchers developed a new dietary counseling plan for six months. This includes four individual consultations, five group meetings and three 24h-recalls. In these six months, participants receive dietary counseling focused on energy restriction (-500 kcal), higher protein intake (aim towards 1.2 g\u002Fkg\u002Fd, minimum of 0.8 g\u002Fkg\u002Fd). Participants are randomly allocated either to the more plant-based diet (≥60%) or the more animal-based diet (≥60%). At the start of the intervention, participants are provided with a workbook and recipe book.\n\nSecondary objectives are to assess the effect after three and six months 2EAT dietary treatment on 1) weight loss and 2) skeletal muscle mass. Exploratory objectives are to assess the effect after three and six months 2EAT dietary treatment on 1) physical health outcomes (muscle mass and physical performance), 2) body composition, 3) metabolic blood parameters, 4) vitality and quality of life, 5) nutritional intake, 6) behavioral changes, 7) evaluate the process of the dietary treatment.",[26],"Obesity",[26,28],"Ageing","RECRUITING","2026-02-17",{"date":32,"type":33},"2026-02-24","ACTUAL",{"date":35,"type":33},"2024-08-13",{"date":37,"type":20},"2027-04-01",{"name":39,"class":40},"Amsterdam University of Applied Sciences","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":40,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":49,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":66},"100504968","effect-of-occupational-therapy-at-home-e-rehabilitation-other-for-persons-post-stroke-100504968","NCT05855226","Effect of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke","Supporting Daily Functioning of Persons With a Neurological Disorder: (Cost)Effectiveness of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke","Inclusion Criteria:\n\n* be able to walk a few steps with or without a walking device.\n* 60 years or older\n* an assessment score of at least 16 on the Montreal Cognitive Assessment (MoCA)\n* an indication for follow up GR at home\n\nExclusion Criteria:\n\n* Who are terminally ill\n* Who have severe aphasia; problems with understanding.\n* Who has been assessed legally incapable by a geriatric doctor","60 Years",{"count":51,"type":20},171,[23],"The goal of this (cost)effectiveness study is to compare care as usual with OTHER-intervention in Cerebro Vascular Accident (CVA) older adults in Geriatric Rehabilitation (GR). The main question\\[s\\] it aims to answer are:\n\n1. What is the effectiveness of OTHER, as compared to occupational therapy as usual (CAU), on improving the self-perceived performance in daily activities of community-dwelling older persons post-stroke over a 24-week period after initiation of OTHER or CAU, as measured longitudinally (at week 4, 13 and 26)?\n\n   Secondary:\n2. What is the effectiveness of OTHER on improving satisfaction with the perceived daily performance of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n3. What is the effectiveness of OTHER on improving physical activity of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n4. What is the effectiveness of OTHER on improving self-management of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n5. How do persons post-stroke and OT's experience and how do they reflect on OTHER in supporting a sense of self-management, safety and improving daily functioning? (qualitative approach).\n6. What factors influenced the intervention delivery and the perceived benefits in the OTHER study (process evaluation)? 1) monitoring treatment fidelity, barriers and facilitators for implementation; 2) gain insight into the impact of OTHER on the GR transition to home; 3) to gain insight into what stroke survivors and OT's think of OTHER. 4) how participants, and professionals experience and thoughts they have on the OTHER-intervention in supporting daily functioning and self-management\n\n   Cost-effectiveness\n7. What is the cost-effectiveness of OTHER on improving self-perceived performance in daily activities and Quality Adjusted Life Years (QALYs) of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n\nParticipants will get the OTHER-intervention treatment given by de occupational therapist which consists of activity monitoring, coaching and videoconferencing to optimalise the transition from clinical care to home.\n\nResearchers will compare care as usual to see if there is a effect on improving the self-perceived performance in daily activities, self-management and improving physical activity .",[55,56,57],"Stroke","eHealth","Occupational Therapy","2025-09-04",{"date":60,"type":33},"2025-09-10",{"date":62,"type":33},"2023-03-13",{"date":64,"type":20},"2026-01",{"name":39,"class":40},9,{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":74,"sex":16,"minAge":75,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":21,"phases":79,"briefSummary":80,"conditions":81,"keywords":4,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":4},"100561609","a-study-on-an-educational-tool-for-the-development-of-a-tailored-dynamic-school-day-in-dutch-primary-schools-100561609","NCT06592391","A Study on an Educational Tool for the Development of a Tailored Dynamic School Day in Dutch Primary Schools.","Process Evaluation and Effectiveness Trial to Assess a Tailored Whole School Approach for a More Dynamic School Day in Dutch Primary Schools.","Inclusion Criteria:\n\nFrom participating 21 schools:\n\n* all teachers\n* a board member\n* all pupils from grade 4 - 8 (Dutch system, age 8 - 12)\n\nExclusion Criteria:\n\n\\-",true,"8 Years","99 Years",{"count":78,"type":20},980,[23],"A dynamic school day is a school day that involves regular interruptions of sedentary learning with moments of physical activity. Many Dutch primary schools have thus far not succeeded in making their school day more 'dynamic' .\n\nIn this project, the researchers will develop an educational innovation to support schools in the development of a dynamic school day that is tailored to their local context. To determine the effectiveness of the educational innovation, the researchers will study the implementation process and assess the effectiveness.\n\nThe research questions for the researcher project are:\n\n1. To what extend are school teams successful in the development and implementation of a tailored dynamic school day, and what are facilitating and hindering factors during implementation?\n2. What is the effect of the tailored dynamic school day on 8 - 12 year old pupils? Sedentary time and physical activity behavior, wellbeing and in class behavior will be assessed.",[82,83],"Physical Activity","Children, Only","NOT_YET_RECRUITING","2024-09-09",{"date":87,"type":33},"2024-09-19",{"date":89,"type":20},"2024-10",{"date":91,"type":20},"2028-01",{"name":39,"class":40},""]