بيتا
رادار التجارب AI
حالة التجربة السريرية NCT06214221 (SWEET) لـ زيادة الوزن والسمنة، متلازمة الأيض، فقدان الوزن هي نشط (التجنيد مغلق). اطلعوا على جميع التفاصيل في عرض البطاقة الخاص برادار التجارب السريرية وأدوات اكتشاف الذكاء الاصطناعي. أو يمكنكم طرح أي سؤال هنا.
تجربة واحدة تطابق معايير الفلتر
عرض البطاقة

Using Signos mHealth Platform in Adults for Weight Management (SWEET)

نشط (التجنيد مغلق)
تفاصيل التجربة السريرية متاحة بشكل أساسي باللغة الإنجليزية. ومع ذلك، يمكن لـ 'رادار التجارب AI' أن يساعدك؛ ما عليك سوى النقر على 'وصف الدراسة' لعرض ومناقشة معلومات التجربة باللغة التي اخترتها.
التجربة السريرية NCT06214221 (SWEET) هي دراسة تدخُّلية لـزيادة الوزن والسمنة، متلازمة الأيض، فقدان الوزن وهي نشط (التجنيد مغلق). بدأت في ٢٠ جمادى الآخرة ١٤٤٥ هـ مع خطة لتجنيد ٣٨٠ مشاركًا. يقودها Signos Inc، ومن المتوقع اكتمالها بحلول ١٣ ذو القعدة ١٤٤٧ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٥ ربيع الآخر ١٤٤٦ هـ.
الملخص
Metabolic syndrome and resulting downstream health effects remains a growing health concern. In published trials, the use of continuous glucose monitoring (CGM) assists behavioral changes efforts, leading to improved adherence and results from diet and exercise changes in individuals with obesity. Mobile health (mHealth) platforms provide satisfactory, easy-to-use tools that help participants in the pursuit of weight change goals. The investigators hypothesize that the use of CGM data and targeted coaching and nutrition education will assist with weight optimization goals in the general (non-diabetic) population using the Signos mHealth platform, with associated health benefits.
وصف مفصل
The scope of this study is to enroll participants into a study that utilizes a continuous glucose monitor (CGM) and mobile health application [Signos] to optimize general wellness and body weight and composition. The Signos users will be compared against a control arm.
العنوان الرسمي

A Randomized Controlled Trial Evaluating the Safety and Effectiveness of the Intelligently-Driven Signos System for Personalized Weight Management in Overweight and Obese Adults

الحالات الطبية
زيادة الوزن والسمنةمتلازمة الأيضفقدان الوزن
المنشورات
مقالات علمية وأوراق بحثية منشورة حول هذه التجربة السريرية:
معرّفات دراسة أخرى
  • SWEET
  • SIGNOS-CGM-SWEET-301-2023
NCT معرّف
تاريخ البدء (فعلي)
2024-01-02
آخر تحديث مُنشور
2024-10-08
تاريخ الاكتمال (المقدر)
2026-04-30
عدد المشاركين المخطط لهم
٣٨٠
نوع الدراسة
تدخُّلية
المرحلة
غ/م
الحالة
نشط (التجنيد مغلق)
الغرض الأساسي
العلاج
طريقة توزيع المشاركين
عشوائي
نموذج التدخل
التصميم المتوازي
التعمية
لا شيء (مفتوحة)
مجموعات/التدخلات
مجموعة المشاركين/مجموعةتَدَخُّل/علاج
تجريبيةSignos System
For all consented participants, the Signos app will use CGM data to provide recommendations customized to users for promoting general health and wellness.
Signos System
The intervention involves the use of the Signos System, a combination of a proprietary software application with a continuous glucose monitor (CGM), to manage weight in overweight and obese adults.
مقارن نشطStandard Lifestyle Education
The "Active Comparator: Standard Lifestyle Education" arm in the clinical trial refers to a control group that receives conventional lifestyle modification advice instead of the experimental Signos System.
Standard Lifestyle Education
In the "Standard Lifestyle Education" arm, participants receive conventional advice on diet and exercise, focusing on general healthy lifestyle habits to manage weight.
النتيجة الرئيسية
مقياس النتيجةوصف القياسالإطار الزمني
Responder Rate
Investigators will measure how many participants successfully reached their weight management goals by the end of 6 months. This 'Responder Rate' tells us the percentage of people in our study who effectively managed their weight using the methods we provided, whether it's through the Signos System or standard lifestyle education.
6 Months
Average Total Body Weight Loss (TBWL%)
Investigators will measure how much weight, on average, participants have lost after 6 months in the study. This will be calculated as a percentage of their initial weight. This measure helps us understand the effectiveness of the Signos System in helping participants reduce their body weight over a 6-month period.
6 Months
معايير الأهلية

الأعمار المؤهلة للدراسة
بالغ, كبار السن
العمر الأدنى للدراسة
22 Years
الجنس المؤهل
الكل
يقبل المتطوعين الأصحاء
نعم

To join our study, participant need to:

  • Be at least 22 years old.
  • Be overweight or obese, which we define as having a Body Mass Index (BMI) between 25 and 40.
  • HbA1c test result should be below 6.5% at the start of the study.
  • Have and know how to use a smartphone that's compatible with the Signos app.
  • Be able to understand, speak, and read English well enough to participate fully in the study.

Participant can't join our study if participant has:

  • Have Type 1 or Type 2 diabetes.
  • Are already using a device to monitor glucose level.
  • Have severe allergies to the sticky part of glucose monitors.
  • Suffer from an eating disorder like anorexia or bulimia.
  • Are currently taking certain medications for diabetes or weight loss.
  • Have had or are planning to have weight loss surgery.
  • Have major health issues like severe kidney disease, untreated thyroid problems, or skin conditions where the glucose monitor would be placed.
  • Have been part of another clinical trial recently.
Signos Inc logoSignos Inc
Lindus Health, Inc. logoLindus Health, Inc.
الجهة المسؤولة عن الدراسة
Stephanie Kim, M.D., MPH, المحقق الرئيسي, Clinical Trial Investigator, Signos Inc
لا توجد بيانات اتصال.
5 مواقع الدراسة في 1 بلدان

Arizona

Helios Clinical Research (Phoenix), Phoenix, Arizona, 85028, United States

California

Diablo Clinical Research, Walnut Creek, California, 94598, United States

Florida

Segal Trials, North Miami, Florida, 33161, United States

Texas

Helios Clinical Research, Houston, Texas, 77008, United States

Washington

Seattle Clinical Research, Seattle, Washington, 98105, United States