[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"diabetes-distress\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:diabetes-distress":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,44,73,101,133,173,227,249,278,297,321],{"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":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100584262","achieving-routine-intervention-and-screening-for-emotional-health-100584262",false,"NCT06887049","Achieving Routine Intervention and Screening for Emotional Health","ARISE: Achieving Routine Intervention and Screening for Emotional Health: Randomized Controlled Trial","ARISE","Inclusion Criteria:\n\n* Patient at a participating clinic\n* Type 2 diabetes\n* Adult (18 years or older)\n* A1C \\> 8%\n\nExclusion Criteria:\n\n* Pregnant","ALL","18 Years",{"count":20,"type":21},1250,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this project is to evaluate the effectiveness of diabetes distress screening and intervention on patients with type 2 diabetes mellitus (T2DM).",[27,28],"Type 2 Diabetes Mellitus (T2DM)","Diabetes Distress",[30],"diabetes distress screening","RECRUITING","2026-06-03",{"date":34,"type":35},"2026-06-05","ACTUAL",{"date":37,"type":35},"2026-03-10",{"date":39,"type":21},"2028-09",{"name":41,"class":42},"University of Chicago","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100588045","type-1-diabetes-and-diabetes-distress-100588045","NCT06936280","Type 1 Diabetes and Diabetes Distress","A Group-based Psychological Intervention for Emerging Adults With Type 1 Diabetes and Diabetes Distress","ACTnow","Inclusion Criteria:\n\n* Type 1 diabetes for at least 6 months\n* Age between 18 and 35\n* T1-DDS score ≥ 2, or T1-DDS subscale score ≥ 2\n* Treated in a diabetes clinic in the Region of Southern Denmark\n* Proficient in Danish\n\nExclusion Criteria:\n\n* Psychiatric diagnosis: diagnosed with substance abuse, alcohol abuse, psychosis, schizophrenia or any other psychiatric diagnosis that may compromise participation in the intervention\n* Cognitive disorders such as brain injury\n* Complex challenges best suited to individual treatment\n* Current therapeutic treatment for depression, anxiety or stress\n* Not stable medication for anxiety\u002Fdepression for the past two months or planned change in medication for anxiety\u002Fdepression during the project period","35 Years",{"count":54,"type":21},100,[24],"The goal of this clinical trial is to reduce diabetes distress in emerging adults (18-35 years) with type 1 diabetes and moderate-to-severe diabetes distress.\n\nThe expectation is that a group-based psychological intervention (ACTnow) will not only reduce diabetes distress but also improve psychological well-being and glycemic outcomes.\n\nThe intervention involves a multidisciplinary team, including nurses, psychologists, and physicians, and is designed in a format that can easily be integrated into future standard care.\n\nThe main research questions are:\n\n* Does a group-based psychological intervention reduce diabetes distress?\n* Does a group-based psychological intervention improve psychological well-being and glycemic outcomes?\n\nResearchers will compare the group-based psychological intervention (arm 1) with a waitlist control group, which will receive the intervention after three months (arm 2).\n\nParticipants will first attend a virtual screening interview with a psychologist or nurse to identify if they are eligible to participate in the study. After randomization, the intervention group receives six bi-weekly sessions, each lasting two hours, led by a psychologist and nurse. Each session includes a mindfulness exercise, a review of the previous session, a new topic, individual homework assignments, and a conclusion.",[28,58],"Diabetes Mellitus Type 1",[60,61,62,50],"RCT study","type 1 diabetes","diabetes distress","2026-04-08",{"date":65,"type":35},"2026-04-09",{"date":67,"type":35},"2025-04-01",{"date":69,"type":21},"2027-05-31",{"name":71,"class":42},"Odense University Hospital",3,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":43},"100606923","technology-enabled-collaborative-care-for-diabetes-and-mental-health-100606923","NCT07181863","Technology-Enabled Collaborative Care for Diabetes and Mental Health","Bridging Gaps, Enhancing Wellbeing: Examining the Effectiveness of the Technology-Enabled Collaborative Care for Diabetes and Mental Health (TECC-DM) Model","TECC-DM","Inclusion Criteria:\n\n* Adults ≥18 years old\n* Diagnosed with type 2 diabetes (T2D)\n* Experiencing mental health challenges, defined as:\n* Hospital Anxiety and Depression Scale (HADS) score ≥8 on either subscale OR\n* Diabetes Distress Scale (DDS) score ≥2\n* Community-living\n* Able to communicate verbally in English\n* Residing in Ontario during study participation\n\nExclusion Criteria:\n\n* Diagnosis of severe mental illness (e.g., schizophrenia, psychotic disorder)",{"count":82,"type":21},160,[24],"Managing both type 2 diabetes and mental health challenges can be difficult, and many people do not receive care that supports both. This study looks at how virtual health coaching and support from interdisciplinary care teams can help people better manage their health.\n\nThe purpose of this study is to test the effectiveness of a virtual health coaching program for adults living with type 2 diabetes and mental health challenges compared to usual care. The Technology-Enabled Collaborative Care for type 2 Diabetes and Mental health (TECC-DM) program includes weekly coaching calls, support from an interdisciplinary care team, and online tools to aid self-management. The findings from this study will be used to help improve services for people who have type 2 diabetes and co-occurring mental health symptoms.",[86,87,28],"Type 2 Diabetes","Mental Health",[89,62,90,91],"type 2 diabetes","technology","collaborative care","2026-03-28",{"date":94,"type":35},"2026-04-02",{"date":96,"type":35},"2025-03-16",{"date":98,"type":21},"2027-12",{"name":100,"class":42},"McMaster University",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":17,"minAge":109,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":22,"phases":113,"briefSummary":114,"conditions":115,"keywords":120,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":43},"100628036","development-and-validation-of-psycho-social-program-psp-100628036","NCT07456410","Development and Validation of Psycho-Social Program (PSP)","Development and Validation of Psycho-Social Program (PSP) for Mental Health Problems Among Patients With Type 2 Diabetes Mellitus (T2DM): A Randomised Controlled Trial","PSP-T2DM","Inclusion Criteria: Participants must be adults aged 30-40 years with Type 2 diabetes, experiencing mild-to-moderate mental health problems related to diabetes will be eligible.\n\nExclusion Criteria: Participants will be excluded if they have severe psychiatric disorders, serious medical comorbidities, are taking psychiatric medications that may affect outcomes, or are unable to participate in the intervention sessions.\n\n\\-","30 Years","40 Years",{"count":112,"type":21},80,[24],"The study aims to determine the effectiveness of a structured psycho-social program (PSP) in improving mental health outcomes among patients with Type 2 diabetes mellitus (T2DM). The intervention is designed to reduce symptoms of depression, anxiety, and diabetes-related distress (DD) by addressing maladaptive thoughts, emotional responses, and coping behaviors associated with chronic illness management. Through structured sessions incorporating cognitive restructuring, stress management techniques, behavioral activation, and adaptive coping strategies, participants will learn to manage emotional distress more effectively while improving treatment adherence and daily functioning. The intervention is expected to enhance psychological well-being, promote healthier coping mechanisms, and support better overall adjustment to living with T2DM.",[116,117,28,118,119],"Mental Health Issue","Depression","Quality of Life","Medication Adherence",[121,122],"Type 2 Diabetes Mellitus","mental health problems","NOT_YET_RECRUITING","2026-03-04",{"date":126,"type":35},"2026-03-06",{"date":128,"type":21},"2026-03-25",{"date":130,"type":21},"2026-08-28",{"name":132,"class":42},"Government College University Faisalabad",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":139,"eligibilityCriteria":140,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":141,"enrollmentInfo":142,"targetDuration":4,"studyType":22,"phases":144,"briefSummary":145,"conditions":146,"keywords":148,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":43},"100617993","digital-self-management-education-and-support-for-young-adults-with-type-2-diabetes-dsmesyat2dm-100617993","NCT07325838","Digital Self-Management Education and Support for Young Adults With Type 2 Diabetes (DSMESYAT2DM)","The Effect of a Digital Self-Management Education and Support Program on Self-Management, Glycemic Control, and Distress in Young Adults With Type 2 Diabetes Mellitus","DSMESYAT2DM","Inclusion Criteria:\n\n* Age between 18 and 45 years.\n* Diagnosis of Type 2 Diabetes Mellitus.\n* Able to read and write in the study language.\n* Has access to the internet and to a digital device (such as a smartphone, tablet, or computer).\n* No communication barriers (e.g., hearing, speech, or severe cognitive impairment that would prevent understanding of the intervention and questionnaires).\n* No physical or mental health condition that, in the opinion of the investigators, would prevent participation in the digital intervention and follow-up.\n* Willing and able to use a digital platform\u002Fapplication for diabetes self-management education and support.\n* Provides informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Diagnosis of Type 1 Diabetes Mellitus or gestational diabetes.\n* Advanced diabetic retinopathy or other severe visual impairment that significantly limits the ability to use digital devices or read educational materials.\n* Severe psychiatric disorder or cognitive impairment that would interfere with participation in the intervention or completion of study assessments.\n* Any condition that the investigators judge to make the person unsuitable for participation (e.g., severe acute illness, terminal condition).\n* Unwillingness or inability to use the digital platform or to share necessary clinical data for the purposes of the study.","45 Years",{"count":143,"type":21},72,[24],"This randomized controlled trial will evaluate the effect of a nurse-led digital self-management education and support program on self-management behaviors, glycemic control, and diabetes-related distress in young adults with Type 2 Diabetes Mellitus (T2DM).\n\nYoung adults with T2DM often have difficulty maintaining good glycemic control and following self-management recommendations. Digital tools and remote education may help support their daily self-care, but there is limited evidence for structured, nurse-led digital programs in this age group.\n\nIn this study, 72 young adults aged 18 to 45 years with T2DM will be recruited from the Endocrinology and Metabolism outpatient clinic of Van Regional Training and Research Hospital. Participants who meet the inclusion criteria and provide informed consent will be randomly assigned to either the intervention group or the active control group (36 participants in each group). Randomization will be stratified by baseline HbA1c level.\n\nThe intervention group will receive a 12-week nurse-led Digital Diabetes Self-Management Education and Support (DSMES) program delivered via a digital platform. The program will be based on the ADCES7™ self-care behaviors and will include structured educational modules, self-monitoring and goal-setting tools, reminders, motivational messages, and interactive communication with a diabetes nurse and, when needed, other members of the multidisciplinary team.\n\nThe active control group will receive usual diabetes care and access to standard digital written education materials (for example, the Ministry of Health Type 2 Diabetes Mellitus patient education brochure in PDF format) via the same platform, as well as basic data entry tools for tracking glucose and related information. However, they will not receive the structured nurse-led DSMES intervention.\n\nPrimary outcomes will include changes in diabetes self-management behaviors and glycemic control (for example, HbA1c) from baseline to the end of the 12-week intervention. Secondary outcomes will include changes in diabetes-related distress and user satisfaction and usability of the digital program. Data will be collected using validated questionnaires and clinical laboratory results obtained from the hospital records.\n\nThe findings of this study may provide evidence on the effectiveness of a nurse-led digital DSMES program in improving self-management, glycemic control, and distress among young adults with T2DM and may support the integration of digital education and support into routine diabetes care.",[27,147,28],"Diabetes-related Distress",[121,149,150,151,152,153,154,155,156,28,157,158,159,160,161,162],"Young Adults","Diabetes Self-Management","Self-Management Education","Digital Health","eHealth","mHealth","Telehealth","Nurse-Led Intervention","Glycemic Control","HbA1c","DSMES (Diabetes Self-Management Education and Support)","Diabetes Education","Randomized Controlled Trial","Behavioral Intervention","2026-01-03",{"date":165,"type":35},"2026-01-08",{"date":167,"type":21},"2026-06-16",{"date":169,"type":21},"2027-12-31",{"name":171,"class":172},"Recep Turan","OTHER_GOV",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":177,"acronym":178,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":180,"enrollmentInfo":181,"targetDuration":4,"studyType":183,"phases":4,"briefSummary":184,"conditions":185,"keywords":205,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":222,"completionDateStruct":224,"leadSponsor":225,"locationsCount":72},"100609246","precision-subclassification-of-mental-health-in-diabetes-digital-twins-for-precision-mental-health-to-track-subgroups-100609246","NCT07212075","Precision Subclassification of Mental Health in Diabetes: Digital Twins for Precision Mental Health to Track Subgroups","TwinPeaks","Inclusion Criteria:\n\n* 18 to 80 years of age\n* Diagnosis of type 1 diabetes or type 2 diabetes or other specific type of diabetes\n* Diabetes duration ≥ 1 year\n* Sufficient German language skills\n* Informed consent\n\nExclusion Criteria:\n\n* Inability to consent\n* Significant cognitive impairment (e.g. dementia)\n* Severe disorder or condition impacting the person's ability to participate in the study or likely to confound results (e.g. treated cancer, heart disease ≥ NYHA III, schizophrenia\u002Fpsychotic disorder)\n* Terminal illness\n* Being bedridden","80 Years",{"count":182,"type":21},1809,"OBSERVATIONAL","Mental conditions and disorders (e.g. distress, depressive, anxiety, and eating disorders) are more prevalent in people with diabetes (PWD) and associated with reduced quality of life and impaired glycaemic outcomes. Evidence supports a complex network between psychosocial factors and glycaemic control that can be highly variable between persons. It is assumed that subgroups exist that show different trajectories of glycaemia and mental health.\n\nBelonging to a particular subgroup may be linked with a higher risk of developing mental health problems compared to others. This suggests that it is possible to treat individuals in different subgroups in a manner that optimizes their treatment and can improve health outcomes. Accurate characterisation can inform more individualized care. This calls for a more personalised approach considering the idiosyncrasies of different subgroups.\n\nOver 3 years, the investigators have established the basis of a precision mental health approach for diabetes using n-of-1 analyses. By utilizing combined ecological momentary assessment (EMA: repeated daily sampling of psychosocial factors in everyday life) and continuous glucose monitoring (CGM), intensive longitudinal data per person could be collected. This enables the analysis of individual associations between glycaemic parameters and psychosocial variables and identification of individual sources of diabetes distress in each person.\n\nThe objective of the present study is to use of the n-of-1 approach to identify subgroups of PWD who share common characteristics in the associations between glucose and psychosocial variables. The identified subgroups shall be used to develop a digital twin for precision mental health in diabetes. The digital twin serves as representation of a real person, allowing to make simulations and predictions of the course of mental health and glycaemia. These predictions can inform diabetes care and lead to more precise, personalised treatment decisions.\n\nTo achieve this, a longitudinal panel including over 1,400 PWD who continuously complete EMA and questionnaire surveys and measure glucose levels using CGM was developed. Over 1000 clinical interviews to diagnose mental disorders have been conducted to identify major mental health conditions and map mental outcomes. To identify subgroups and develop the digital twin, the sampling will be expanded aiming at a total of 1,809 PWD. Incidence and remission of mental disorders will be determined via repeated interviews.\n\nThe complex networks between clinical, metabolic, and psychosocial data will be analysed using machine learning, leading to new insights with the potential to shape future guidelines. These results will be used by the digital twin to predict courses of glycaemic control and mental health, translating the individual evidence into direct treatment suggestions.",[186,187,188,189,28,190,191,192,193,194,195,196,197,198,199,200,201,202,203,204],"Diabetes (DM)","Diabete Mellitus","Diabete Type 1","Diabete Type 2","Diabetes Complications","Depression - Major Depressive Disorder","Depression Anxiety Disorder","Depression Bipolar","Depression Disorders","Anxiety Disorder (Panic Disorder or GAD)","Anxiety Disorder NOS","Eating Disorder Binge","Anorexia Nervosa","Bulimia Nervosa","Eating Disorder Not Otherwise Specified","Depressed Mood","Anxiety Symptoms","Disordered Eating Behaviors","Fear of Hypoglycemia",[206,207,208,209,210,211,212,213,214,215,216,158,117,217,218,28,178],"Digital Twin","Precision Medicine","Precision Mental Health","Subclassification","Trajectories","Subtypes","Person-reported Outcomes (PRO)","Ecological Momentary Assessment (EMA)","Continuous Glucose Monitoring (CGM)","People with Diabetes (PWD)","Diabetes Mellitus","Anxiety","Eating disorder","2025-11-27",{"date":221,"type":35},"2025-12-04",{"date":223,"type":35},"2025-01-01",{"date":169,"type":21},{"name":226,"class":42},"Forschungsinstitut der Diabetes Akademie Mergentheim",{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":232,"acronym":4,"eligibilityCriteria":233,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":234,"targetDuration":4,"studyType":22,"phases":236,"briefSummary":237,"conditions":238,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":245,"leadSponsor":247,"locationsCount":4},"100601475","diabetes-distress-and-quality-of-life-in-university-students-with-type-1-dm-100601475","NCT07110974","Diabetes Distress and Quality of Life in University Students With Type 1 DM","Assessment of Diabetes Distress and Quality of Life in Sohag University Students With Type 1 Diabetes Mellitus","Inclusion Criteria:\n\n1. Already diagnosed Type 1 diabetes mellitus\n2. receiving insulin\n\nExclusion Criteria:\n\n1. refuses to participate in the study.\n2. deaf or mute.",{"count":235,"type":21},200,[24],"This study aims to encourage and support Sohag University Students with type 1 Diabetes Mellitus (T1DM). It will discover students with poor glycemic control, diabetic retinopathy, and renal complications. In addition to focus on those students suffering from Diabetes Distress (DD) and poor Quality of Life (QOL) due to type 1 Diabetes Mellitus (T1DM).",[239,28],"Diabetes Type 1","2025-08-01",{"date":242,"type":35},"2025-08-08",{"date":244,"type":21},"2025-10",{"date":246,"type":21},"2026-10",{"name":248,"class":42},"Sohag University",{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":255,"eligibilityCriteria":256,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":257,"enrollmentInfo":258,"targetDuration":4,"studyType":22,"phases":260,"briefSummary":261,"conditions":262,"keywords":264,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":274,"leadSponsor":276,"locationsCount":43},"100577930","technology-enabled-collaborative-care-for-young-adults-with-type-1-diabetes-and-diabetes-distress-a-feasibility-trial-100577930","NCT06804694","Technology-Enabled Collaborative Care for Young Adults With Type 1 Diabetes and Diabetes Distress: A Feasibility Trial","Technology-Enabled Collaborative Care for Young Adults With Type-1 Diabetes and Diabetes Distress (TECCT1D3): Feasibility Trial of a Co-designed Intervention","TECC-T1D3","Inclusion Criteria:\n\n* Young adult (age 18-29 years)\n* Resident of Ontario\n* Living with a self-reported diagnosis of T1D of at least 1 year\n* Individual is community-living (people who live independently in the community and are not residing in a setting that provide institutional care or support)\n\nExclusion Criteria:\n\n* Unable to participate in English language\n* Unable to participate via telephone or web-conferencing","29 Years",{"count":259,"type":21},60,[24],"The goal of the study is to evaluate the acceptability and feasibility of a co-designed, Technology-Enabled Collaborative Care for Young Adults with Type-1 Diabetes and Diabetes Distress (TECC-T1D3) program. Through this program, the investigators aim to deliver a collaborative care intervention, featuring a health coach and a virtual care team, designed to help participants manage mental health and overall wellbeing.",[263,28],"Type 1 Diabetes (T1D)",[265,266,28,267,268],"Type 1 Diabetes","TECC model","Technology-enabled Care","Young adults with T1D","2025-01-27",{"date":271,"type":35},"2025-02-03",{"date":273,"type":35},"2024-11-27",{"date":275,"type":21},"2025-09",{"name":277,"class":42},"Centre for Addiction and Mental Health",{"id":279,"slug":280,"hasResults":11,"nctId":281,"briefTitle":282,"officialTitle":282,"acronym":4,"eligibilityCriteria":283,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":284,"targetDuration":4,"studyType":22,"phases":286,"briefSummary":287,"conditions":288,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":289,"lastUpdatePostDateStruct":290,"startDateStruct":292,"completionDateStruct":293,"leadSponsor":295,"locationsCount":43},"100546680","developing-and-testing-a-self-compassion-tool-kit-to-improve-the-care-of-individuals-with-type-2-diabetes-100546680","NCT06398093","Developing and Testing a Self-Compassion Tool Kit to Improve the Care of Individuals With Type 2 Diabetes","Inclusion Criteria:\n\n* Has type 2 diabetes\n* Has a score above 2 on the T2D Distress Assessment Scale\n\nExclusion Criteria:\n\n* Does not have type 2 diabetes\n* Has a score above 2 on the T2D Distress Assessment Scale\n* Cannot safely exercise\n* Cannot complete the requested tasks",{"count":285,"type":21},30,[24],"There is a high prevalence of anxiety and depression in patients with Type 2 Diabetes (T2D). While past studies demonstrate the potential therapeutic effect of mindfulness-based interventions in patients with T2D, little is understood about the mode of delivery or quantity of the intervention necessary to experience benefits. This project aims to develop and implement a self-compassion tool kit based on the principles of mindfulness and meditation to better understand how self-compassion works to affect psychological health and wellbeing in patients with T2D. The investigators will study the impact of a self-compassion tool kit - including mindfulness meditation, exercise, journaling and sleep parameters - on T2D. Enhancing emotional well-being could complement current T2D treatments to facilitate improved quality of life.",[86,28],"2024-07-15",{"date":291,"type":35},"2024-07-17",{"date":289,"type":35},{"date":294,"type":21},"2024-09",{"name":296,"class":42},"University of California, San Diego",{"id":298,"slug":299,"hasResults":11,"nctId":300,"briefTitle":301,"officialTitle":302,"acronym":4,"eligibilityCriteria":303,"healthyVolunteers":11,"sex":17,"minAge":109,"maxAge":4,"enrollmentInfo":304,"targetDuration":4,"studyType":22,"phases":306,"briefSummary":307,"conditions":308,"keywords":310,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":313,"lastUpdatePostDateStruct":314,"startDateStruct":316,"completionDateStruct":318,"leadSponsor":320,"locationsCount":43},"100549624","use-of-an-online-intervention-for-the-treatment-of-diabetes-distress-in-patients-with-type-1-diabetes-100549624","NCT06436456","Use of an Online Intervention for the Treatment of Diabetes Distress in Patients With Type 1-Diabetes","The Feasibility, Acceptability and Preliminary Effectiveness of an Internet-based Intervention for Diabetes Distress in Patients With Type 1 Diabetes","Inclusion Criteria:\n\n* A total score or a score on one of the subscales of the Diabetes Distress Scale for type 1 diabetes which is 2 or above.\n* Diagnosed with type 1-diabetes ≥ 12 months ago.\n* Age ≥ 30 years.\n* Receiving treatment at SDCO.\n* Proficiency in Danish and basic IT skills.\n\nExclusion Criteria:\n\n* Psychiatric diagnosis that may compromise participation in the intervention e.g. psychosis, schizophrenia, substance or alcohol abuse.\n* Cognitive impairments that may compromise participation in the intervention e.g. dementia, Alzheimer's, brain injury.\n* Complex issues best suited for individual treatment as assessed by the clinical psychologist.",{"count":305,"type":21},40,[24],"This study will investigate whether an online intervention can be helpful in reducing diabetes distress in people with type 1 diabetes and elevated diabetes distress, compared to individual counselling sessions (online, phone-based or face-to-face, depending on the preference of the person with type 1 diabetes). Half of the participants will receive the online intervention, while the other half will receive individual counseling sessions with a psychologist.\n\nObjectives: The main aim of this study is to investigate if the online intervention is feasible and liked by people with type 1 diabetes and diabetes distress, in comparison with individual counselling sessions.\n\nHypotheses: The investigators predict that both interventions will be feasible to use, shown by how many people join, stay engaged, and complete the interventions. The investigators also think that people will find both interventions acceptable, as shown by the positive feedback given in interviews after they finish.",[309,28],"Diabetes Mellitus, Type 1",[309,311,312],"Diabetes distress","Online intervention","2024-06-27",{"date":315,"type":35},"2024-06-28",{"date":317,"type":35},"2024-06-20",{"date":319,"type":21},"2025-05-30",{"name":71,"class":42},{"id":322,"slug":323,"hasResults":11,"nctId":324,"briefTitle":325,"officialTitle":326,"acronym":327,"eligibilityCriteria":328,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":329,"targetDuration":4,"studyType":22,"phases":331,"briefSummary":332,"conditions":333,"keywords":4,"overallStatus":123,"whyStopped":4,"lastUpdateSubmitDate":334,"lastUpdatePostDateStruct":335,"startDateStruct":337,"completionDateStruct":339,"leadSponsor":341,"locationsCount":43},"100550535","uk-myremedy-clinical-trial-100550535","NCT06448338","UK MyREMEDY Clinical Trial","MyDiaMate for Remission of Elevated Diabetes Distress in Type 1 Diabetes: the UK MyREMEDY Randomized Controlled Trial","UK-MyREMEDY","Inclusion Criteria:\n\n* At least 18 years old at signing the informed consent form\n* Type 1 diabetes diagnosis at least 6 months ago\n* Having access to the internet and a smartphone\u002Ftablet\u002Flaptop\u002Fcomputer for the entirety of study participation\n* Experiencing diabetes distress (checked during a phone call between research assistant and participant. The condition is met if the participant has an average score of ≥2 on the 2-item Diabetes Distress Scale \\[DDS-2\\], representing clinically meaningful diabetes distress)\n\nExclusion Criteria:\n\n* Having been diagnosed with a psychiatric disorder in the past 6 months for which the person is under psychological\u002Fpsychiatric treatment\n* Suicidality\n* Having started a treatment with psychotropic medication in the past 3 months\n* Cannot read and speak English\n* Experience of cognitive problems that hamper using MyDiaMate or vision\u002Fauditory problems that are hindering in daily life",{"count":330,"type":21},165,[24],"The UK MyREMEDY study investigates whether MyDiaMate, an online self-help program, can effectively improve the mental health of adults with type 1 diabetes compared to those receiving care as usual.",[265,28],"2024-06-07",{"date":336,"type":35},"2024-06-10",{"date":338,"type":21},"2024-07-01",{"date":340,"type":21},"2025-12-01",{"name":342,"class":42},"King's College London"]