[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sophiahemmet University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":100},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100514046","evaluation-of-a-personalised-digital-intervention-evibody-for-healthy-and-sustained-lifestyle-behaviors-and-well-being-among-adults-a-real-world-quasi-experimental-study-100514046",false,"NCT05973383","Evaluation of a Personalised Digital Intervention (EviBody) for Healthy and Sustained Lifestyle Behaviors and Well-being Among Adults: a Real-world Quasi-experimental Study","Effectiveness and Theory-based Evaluation of a Personalised Digital Intervention (EviBody) for Healthy and Sustained Lifestyle Behaviours and Well-being Among Adults","Inclusion Criteria (intervention arms):\n\n* adults ≥18 years\n* signing up for the app EviBody using electronic identification\n* consent to the research study\n\nInclusion Criteria (controls):\n\n* adults ≥18 years\n* consent to the research study\n\nExclusion Criteria (intervention arms):\n\n* individuals who are discharged from the app due to refracting the terms of the service,\n* is currently using a digital product that is explicitly designed to support behaviour change,\n* subjects scoring \\>70 on well-being will be excluded from the primary analyses,\n* subjects who appear as friends, colleagues, or family with anyone in the research or owner group will be excluded.\n\nExclusion Criteria (controls):\n\n* is currently using a digital product that is explicitly designed to support behaviour change,\n* is found to be a user of EviBody,\n* subjects scoring \\>70 on well-being will be excluded from the primary analyses,\n* subjects who appear as friends, colleagues, or family with anyone in the research or owner group will be excluded.",true,"ALL","18 Years",{"count":20,"type":21},1500,"ESTIMATED","OBSERVATIONAL","The goal of this quasi-experimental observational study is to evaluate the impact of a personally tailored digital intervention aimed to support a healthy lifestyle on well-being, lifestyle behaviors, and mental health among the adult population.\n\nThe main questions it aims to answer are:\n\nI) Is a digital intervention developed to offer personalised digital support for healthy habits effective in improving well-being compared to a control group from the general population after 6 months? II) Is the effectiveness dose-dependent (better effect with higher membership level)? III) Does the digital intervention assist in maintaining healthy eating and physical activity habits, mental health, and well-being across 24 months? IV) Are sociodemographic factors associated with achieving the self-identified goals and improvements in eating and physical activity habits, mental health, and well-being? VI) Do engagement, motivation, self-efficacy, and perceived barriers mediate the associations between sociodemographic characteristics and changes in self-identified goals, eating and physical activity habits, mental health, and well-being over a 24-month period? V) How is the pattern of user engagement across 24 months?\n\nParticipants are users of the mobile phone application EviBody. The group will be compared with individuals from the general population to evaluate if the digital intervention is effective in improving well-being, eating and physical activity habits, and mental health.",[25],"Well-being",[27,28,29,30,31],"primary prevention","secondary prevention","health promotion","self-management","behavior","RECRUITING","2026-04-23",{"date":35,"type":36},"2026-04-29","ACTUAL",{"date":38,"type":36},"2026-01-01",{"date":40,"type":21},"2028-12-31",{"name":42,"class":43},"Sophiahemmet University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":64,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":44},"100487939","periodic-continuous-glucose-monitoring-in-patients-with-type-2-diabetes-100487939","NCT05633628","Periodic Continuous Glucose Monitoring in Patients With Type 2 Diabetes","Periodic Continuous Glucose Monitoring to Support a Person-centered Approach During Diabetes Consultations in Patients With Type 2 Diabetes- A Randomised Controlled Study","Inclusion Criteria:\n\n* Adults aged 18-80 years\n* Type 2 diabetes with a duration of \\> 6 months\n* HbA1c 45-70 mmol\u002Fmol\n* Have a smartphone\n* Experience of self-monitoring of blood glucose prior to the study start\n\nExclusion Criteria:\n\n* Prandial insulin\n* Pregnancy or planning pregnancy during the study\n* Breastfeeding\n* Renal disease with estimated glomerular filtration rate (eGFR) \\\u003C45 mL\u002F min\u002F1.73 m2\n* Active malignancy or under investigation for malignancy\n* Severe visual impairment\n* Severe skin allergy that inhibits the use of a continuous glucose monitoring device\n* Glucocorticoids (systemic)\n* Planned or currently using weight reduction medications, programs, or surgery\n* Cognitively or psychologically unable to participate and read instructions\n* Enrolled in other clinical trials\n* Eating disorders","80 Years",{"count":54,"type":21},400,"INTERVENTIONAL",[57],"NA","The aim of this randomised controlled trial is to investigate the effectiveness of periodic CGM (continuous glucose monitoring) to support a person-centered approach versus self-monitoring of blood glucose (SMBG) in adults with type 2 diabetes on glucose control and patient reported outcomes.",[60],"Type 2 Diabetes",[62,63],"CGM","Personcentered care",{"date":35,"type":36},{"date":66,"type":36},"2023-02-01",{"date":68,"type":21},"2026-12",{"name":42,"class":43},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":55,"phases":79,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},"100587962","evaluation-of-a-digital-person-centered-rehabilitation-program-targeting-physical-activity-in-spinal-stenosis-surgery-get-back-100587962","NCT06935201","Evaluation of a Digital Person-Centered Rehabilitation Program Targeting Physical Activity in Spinal Stenosis Surgery (Get Back)","Get Back, A Digital Person-Centered Rehabilitation Program to Increase Physical Activity After Lumbar Spinal Stenosis Surgery - a Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients planned for decompression surgery due to central lumbar spinal stenosis\n\nExclusion Criteria:\n\n* Patients with malignancy under treatment or with metastases;\n* History of neurological or other disorders resulting in severe movement dysfunction;\n* Untreated or instable heart conditions that prohibits physical tests;\n* Poor understanding of Swedish.",{"count":78,"type":21},252,[57],"This study aims to investigate whether Get Back is more effective than standard rehabilitation in increasing the number of steps per day, improving physical activity levels, and functional ability for patients undergoing surgery for lumbar spinal stenosis (LSS). LSS is common, especially among older adults, leading to increased health risks and reduced quality of life. Despite its prevalence (about 60% of all spinal surgeries in Sweden), many LSS patients remain physically inactive post-surgery, worsening their health. Rehabilitation remains a global challenge with unequal access, and many patients feel disengaged from the process. Get Back is a digital rehabilitation program including three components: gradually increasing physical activity, managing fear and avoidance behaviors, and using behavior change techniques. It has shown promising results in a pilot study, increasing daily steps. The program uses a person-centered approach tailored to personal needs. This multicenter randomized controlled trial will assess efficacy, process, and cost-effectiveness. It will also explore how preoperative values such as physical capacity and psychological factors predict changes in daily steps after surgery. Data will be collected via questionnaires, functional tests, and interviews, with the primary outcome being daily steps measured with motion sensors. The study will involve 252 patients from four spinal clinics. Get Back promotes increased physical activity and accessible rehabilitation, contributing to better health for LSS patients.",[82],"Spinal Stenosis Lumbar",[84,85,86,87,88,89,90],"Rehabilitation","Person-centred care","Physical activity","Steps per day","Behavioral medicine","Telerehabilitation","Telehealth","2026-04-22",{"date":93,"type":36},"2026-04-28",{"date":95,"type":36},"2025-05-12",{"date":97,"type":21},"2028-05",{"name":42,"class":43},4,""]