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Completed

NCT Number: NCT05561855

T2DM Intensity Lifestyle Intervention

This RCT study will evaluate the effect of a lifestyle intervention on overweight or obese patients with type 2 diabetes mellitus. The primary hypothesis is that the mHealth-based intensive lifestyle intervention is sufficient to achieve weight loss and maintain glycated hemoglobin control.

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Key information

About this study

Diabetes mellitus is a chronic systemic metabolic disease caused by the long-term interaction of genetic factors and environmental factors. It is characterized by an increase in plasma glucose levels and is mainly due to metabolic disorders in glucose, fat, and protein caused by insufficient insulin secretion and/or dysfunction in the body, which affects normal physiological activities. As of 2019, 463 million people are suffering from diabetes in the world, of which 90% to 95% have type 2 diabetes mellitus (T2DM), with an average of 1 patient in every 11 adults (aged 20-79). The number of patients with T2DM will jump to 700 million by 2045. There is a close relationship between T2DM and overweight and obesity. The prevalence of diabetes in overweight and obese people in China was 12.8% and 18.5%, respectively. Among T2DM patients, the proportions of overweight and obesity were 41% and 24.3%, respectively.The two kinds of diseases share a common key pathophysiological mechanism, which will have a devastating long-term impact on patients' health and bring serious disease and economic burden to the family. Given the various harms, it is urgent to carry out relevant intervention research and formulate effective intervention strategies. With the development of artificial intelligence technology, the combination of mHealth and multidisciplinary lifestyle intervention may become an efficient and easy-to-popularize management mode for the prevention and treatment of T2DM with obesity.

Given the relative lack of high-quality interventions for T2DM overweight/obesity, the investigators designed a randomized controlled trial to assess the effectiveness of a multicomponent intervention in Ningbo First Hospital. This study plans to adopt the online and offline combination method based on mHealth technology to carry out lifestyle intervention aimed at formulating a set of feasible and effective intervention strategies.

The study aims to identify: 1) whether the mHealth-based intensive lifestyle intervention will be effective for weight and glycated hemoglobin management to reverse or slow down the disease process among T2DM patients with overweight/obesity; 2) whether the intervention will be beneficial for improving biochemical indicators, body composition indicators, and exercise capacity among T2DM patients with overweight/obesity.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meet the WHO diagnostic criteria for type 2 diabetes;
  • The duration of diabetes is less than 5 years;
  • HbA1c was between 6.5-11% in recent 3 months;
  • 18-65 years old;
  • 24kg/m2≤BMI#40kg/m2;
  • Weight loss within the past 3 months did not exceed 5% of initial weight;
  • Currently using a smartphone;
  • Voluntary participation.

Exclusion criteria

  • Pregnant or lactating woman, or planning a pregnancy within 6 months after recruitment;
  • Uncontrolled hypertension (resting blood pressure ≥ 160/100mmHg);
  • Treatment with insulin;
  • Acute complications of diabetes (diabetic ketoacidosis, hyperosmolar state, infection. etc) have occurred within the past 3 months, or one or more severe chronic complications of diabetes have existed, such as severe cardiovascular or cerebrovascular pathology (angina pectoris, myocardial infarction, grade III-IV heart failure, severe arrhythmia, transient cerebral ischemic attack, stroke, etc.), massive proteinuria (urinary albumin/creatinine ratio ≥300 mg/g), and severe diabetic foot, severe neuropathy, blurred vision.
  • Currently using weight-reducing products such as orlistat, or other medications that can significantly affect weight such as diuretics and hormones;
  • Severe cardiovascular and cerebrovascular diseases, respiratory diseases, hepatic and renal insufficiency, malignant tumors and other chronic consumptive diseases, active infections, and surgical history involving important organs within 3 months;
  • Contraindications to physical activity;
  • The presence of mental or cognitive impairment;
  • Current participation in other clinical trial projects;
  • Having the same family member involved in the research.

Treatment and study plan

Lifestyle Intervention

Behavioral

During the 3-month lifestyle intervention period, the participants need to complete the weight monitoring, behavioral goal recording, diet and exercise recording, online course learning by using the WeChat official account module of "Weight Loss and Glucose Control".They will receive corresponding feedback and integral rewards every week, and receive monthly follow-ups to complete health education, goal review, motivational interview as well as collecting medication changes and blood glucose monitoring data.

Primary outcomes

  1. Weight change from baseline

    Time frame: at end of the 3-month intervention

    measured in kilograms (kg) and calculate the change percentage(%)

  2. The change of HbA1c from baseline

    Time frame: at end of the 3-month intervention

    measured in percent (%)

Secondary outcomes

  1. The change in body mass index (BMI) from baseline

    Time frame: at end of the 3-month intervention

    Weight and height will be combined to report BMI in kg/m^2.

  2. The change of waist circumference from baseline

    Time frame: at end of the 3-month intervention

    measured in centimetre (cm)

  3. The change of waist-to-hip circumference ratio from baseline

    Time frame: at end of the 3-month intervention

    measure waist circumference and hip circumference to calculate waist-to-hip circumference ratio

  4. The change of both systolic and diastolic blood pressures from baseline

    Time frame: at end of the 3-month intervention

    measure systolic and diastolic blood pressure in millimeters of mercury (mmHg) by using electronic sphygmomanometer

  5. The change of body fat percentage from baseline

    Time frame: at end of the 3-month intervention

    measure body fat percentage (%) by bioelectrical impedance analysis

  6. The change of blood lipids from baseline

    Time frame: at end of the 3-month intervention

    measure total cholesterol, triglyceride, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol in milligram/deciliter (mg/dL)

  7. The change in muscle strength from baseline

    Time frame: at end of the 3-month intervention

    measure grip strength in kilograms (kg) by hand dynamometer

  8. The change in exercise capacity from baseline

    Time frame: at end of the 3-month intervention

    The 3-Minute Step Test is an assessment for Cardiorespiratory Fitness. At the end of the 3 minutes, sit down and monitor the pulse for one full minute. Calculate step-test index with the recovery heart rate. The fitter you are, the quicker the heart rate will return to normal after exercise.

  9. The change in life quality from baseline

    Time frame: at end of the 3-month intervention

    It is measured in the form of the Short form health survey (SF-36), scored from 0 to 100, with higher scores associated with better quality of life.

  10. The change in sleep quality from baseline

    Time frame: at end of the 3-month intervention

    It is measured in the form of the Pittsburgh Sleep Quality Index (PSQI), scored from 0 to 21, with higher scores associated with worse quality of sleep.

  11. The change in depression severity from baseline

    Time frame: at end of the 3-month intervention

    It is measured in the form of the Pittsburgh Sleep Quality Index (PSQI), scored from 0 to 27, with higher scores associated with greater degree of depression.

Sponsors and collaborators

Lead sponsor

Ningbo No. 1 Hospital

Other

Collaborators

  • Peking University

Registry information

Official study title

The Effect of mHealth-Based Lifestyle Intervention on Overweight or Obese Patients With Type 2 Diabetes: A Randomized Controlled Trial

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 30, 2022
Registry last updated
Nov 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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