[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"type-2-diabetes-mellitus-with-complication\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:type-2-diabetes-mellitus-with-complication":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100575326","implementation-of-a-preventive-diabetic-foot-care-program-for-patients-at-risk-of-diabetic-foot-100575326",false,"NCT06770829","Implementation of a Preventive Diabetic Foot Care Program for Patients at Risk of Diabetic Foot","The Effect of a Preventive Diabetic Foot Care Program on Knowledge, Behavior, Self-Management, and Glycemic Control Levels in Patients at Risk of Diabetic Foot","Inclusion Criteria\n\nParticipants must meet all of the following criteria to be included in the study:\n\n* Patients with type 2 diabetes receiving follow-up and treatment at the Akdeniz University Hospital Endocrinology and Metabolic Diseases Outpatient Clinic.\n* Presence of one or more diabetic foot risk factors, categorized as category 2 or 3 according to the IWGDF (International Working Group on the Diabetic Foot) Risk Classification System.\n* Diagnosed with type 2 diabetes for at least six months.\n* Aged between 30 and 65 years.\n* Literate.\n* No physical or mental disabilities that would prevent answering the study questions.\n* No communication barriers.\n* Able to understand and verbalize their diagnosis.\n* HbA1c ≥7.5%.\n* Internet access at home and possession of a device such as a computer, tablet, or smartphone, with the ability to use these tools.\n* Willing to provide informed consent to participate in the study.\n\nExclusion Criteria\n\nParticipants will be excluded if they meet any of the following conditions:\n\n* Myocardial infarction, stroke, heart failure, or angina pectoris within the last year.\n* Diagnosed with type 1 diabetes or gestational diabetes.\n* Presence of an active diabetic foot ulcer.\n* Diagnosed with dementia or cognitive deficits.\n* Diagnosed with glaucoma, cataracts, or retinopathy.\n* Diagnosed with a terminal illness.\n* Inability to provide accurate information or participate in the study.\n\nCriteria for Exclusion During Follow-Up\n\nParticipants will be excluded from the study during the follow-up period if they meet any of the following conditions:\n\n* Voluntarily choose to withdraw from the study.\n* Fail to complete at least two-thirds of the follow-up period for any reason.\n* Undergo bariatric surgery during the study.\n* Exhibit non-adherence to prescribed medications.\n* Have a general health condition that, according to their own statement, is unsuitable for continuing the study.","ALL","30 Years","65 Years",{"count":20,"type":21},78,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the effect of a preventive diabetic foot care program on the knowledge, behavior, self-management, and glycemic control levels of type 2 diabetic patients at risk of diabetic foot. The development of a Preventive Diabetic Foot Care Program (DiaFOOTCare) for patients with type 2 diabetes at risk of diabetic foot is expected to make a significant contribution to preventing diabetic foot formation. The DiaFOOTCare program consists of two stages. In the first phase, a comprehensive, multi-component, and evidence-based preventive diabetic foot care program will be designed specifically for type 2 diabetic patients at risk of diabetic foot. The internal validity of the program will be tested through expert evaluations by specialists in diabetic foot care, assessments using readability formulas, and pre-application testing with patients identified as being at risk of diabetic foot. As part of the final implementation of the first phase, all interventions included in the DiaFOOTCare protocol will be administered to four patients with diabetic foot risk over a three-week period. Following this, the DiaFOOTCare protocol will be evaluated based on the feedback provided by these four pre-application participants. In the second phase, a randomized controlled trial (RCT) with a single-blinded and active control group design will be conducted at the Akdeniz University Hospital Endocrinology and Metabolic Diseases Outpatient Clinic. A group of patients with type 2 diabetes and diabetic foot risk will be identified, and pre-tests will be administered. The patients will then be randomly assigned to the intervention group (n=39) and the control group (n=39). The effectiveness of the DiaFOOTCare program will be assessed through post-tests.",[27,28],"Diabetic Foot Ulcer","Type 2 Diabetes Mellitus With Complication",[30,31,32,33,34],"Nursing","Type 2 Diabetes Mellitus","Diabetic Foot","Preventive Diabetic Foot Care","Randomized Controlled Trial","NOT_YET_RECRUITING","2026-06-09",{"date":38,"type":39},"2026-06-10","ACTUAL",{"date":41,"type":21},"2026-06-15",{"date":43,"type":21},"2026-08-01",{"name":45,"class":46},"Akdeniz University","OTHER",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":18,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100630186","comparing-effects-of-hiit-and-mict-on-functional-mobility-muscle-strength-and-quality-of-life-in-diabetic-patients-100630186","NCT07484399","Comparing Effects of HIIT and MICT on Functional Mobility, Muscle Strength, and Quality of Life in Diabetic Patients","Comparing The Effects of High Intensity Interval Training and Moderate Intensity Continuous Training on Functional Mobility, Muscle Strength, and Quality of Life in Diabetic Patients","Inclusion Criteria\n\n:• Adults aging form 35 to 65.\n\n* Both male and female diabetic patients.\n* Individuals diagnosed with type 2 diabetes for at least five years.\n* Individuals able to participate in moderate to intense physical activity.\n\nExclusion Criteria:\n\n* • Individuals with significant orthopedic limitations.\n\n  * Individuals with uncontrolled cardiovascular disease or musculoskeletal issues.\n  * Individuals with incontinence issues during physical activity or inability to comply to study protocols","35 Years",{"count":56,"type":21},28,[24],"To compare the effects of High-Intensity Interval Training (HIIT) and Moderate-Intensity Continuous Training (MICT) on functional mobility, muscle strength, and quality of life in individuals with type-2-diabetes.",[28],[61],"muscles weakness, disability, reduced quality of life,","2026-03-16",{"date":64,"type":39},"2026-03-20",{"date":66,"type":21},"2026-03-05",{"date":68,"type":21},"2026-09-22",{"name":70,"class":46},"Riphah International University"]