Skip to main content
OpenTrials
Completed

NCT Number: NCT03225339

Diabetes Intervention Accentuating Diet and Enhancing Metabolism

Diabetes is one of the greatest challenges faced by healthcare services worldwide. It is associated with serious complications such as heart attacks, stroke, and peripheral artery disease as well as kidney disease, eye disease, and nerve dysfunction. Data from weight loss with bariatric surgery suggest that with the appropriate intervention, it should be possible to reverse diabetes and that the earlier the intervention occurs, the greater the chances of placing diabetes into remission. There is now a need to translate this knowledge into the medical care of younger patients with early diabetes who are overweight/obese. The aim of this study is to see if younger adult patients with overweight/obesity and type 2 diabetes who are participants in a programme incorporating a low energy diet and physical activity (lifestyle) will lower their weight, cardiovascular risk and improve their glycaemic control as compared to the usual care.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hamad Medical Corporation, Doha, Qatar

Loading trial locations.

About this study

The aim of the proposed study is to conduct a pragmatic randomised controlled clinical trial randomising young adult patients with obesity and type 2 diabetes to an intervention incorporating a low calorie diet and physical activity or usual care. The investigators hypothesise that patients in the low calorie intervention arm will have greater weight reduction leading to significant improvement in glycaemic control and cardiovascular risk. The primary outcome will be weight loss. The low calorie diet intervention arm is designed to achieve and maintain significant weight loss through decreased calorie intake, increased physical activity, and behaviour change. Usual care will include routine advice about diet and physical activity. Secondary outcomes include diabetes control, body composition, and quality of life.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Type 2 diabetes mellitus (based on ADA diagnostic criteria) ;
  • Diabetes of ≤ 3-year duration;
  • BMI >27.0 kg/m² (based on WHO cut-points for ethnicity 119);
  • Men and women;
  • Age 18-50 years;
  • Originating from the Middle East and North Africa region and resident in Qatar;
  • Able to commit to the study duration;
  • Able to give informed consent and willing to participate in the study.

Exclusion criteria

  • Type 1 diabetes mellitus based on clinical history;
  • Cardiovascular event in the previous 6 months;
  • Chronic kidney disease stage 3b or greater (eGFR <30 mL/min/1.73m²);
  • Currently pregnant, lactating, or planning pregnancy within the study period;
  • Any condition precipitating fluid overload such as heart failure (NYHA class > I) and liver cirrhosis;
  • Significant previously diagnosed psychiatric disorder (e.g. schizophrenia, post-traumatic stress disorder, obsessive-compulsive disorder);
  • Uncontrolled depression (based on hospital anxiety and depression scale);
  • Uncontrolled epilepsy;
  • Known lactose intolerance;
  • Severe arthritis preventing walking;
  • Active gout;
  • Active gallstone disease or known asymptomatic gallstones.

Treatment and study plan

Low Energy Diet

Dietary Supplement

Low Energy Diet

Primary outcomes

  1. Weight loss

    Time frame: 12 months

    Weight change (weight in kilograms)

Secondary outcomes

  1. Glycaemic control

    Time frame: 12 months

    HbA1c measured biochemically (percentage units)

  2. Patient reported outcomes

    Time frame: 12 months

    Euro-QoL-5D

Other outcomes

  1. Insulin sensitivity/resistance

    Time frame: 12 months

    Fasting Insulin and Glucose levels will be combined to calculate:

    Homeostatic model assessment (HOMA-IR)

  2. Body Mass Index

    Time frame: 12 months

    Weight and height measures will be used to calculate body mass index: Weight(kg)/(height[m])2

  3. Waist Circumference

    Time frame: 12 months

    Waist Circumference measured in cm

Sponsors and collaborators

Lead sponsor

Weill Cornell Medical College in Qatar

Other

Collaborators

  • Cornell University
  • Hamad Medical Corporation
  • Weill Medical College of Cornell University

Registry information

Official study title

A Randomised Controlled Trial Assessing the Impact of Low Calorie Diet and Activity on Body Weight and Glycaemia in Diabetes

Acronym: DIADEM-1

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Jul 21, 2017
Registry last updated
Apr 8, 2021

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.

Published trials that share one or more normalized conditions with this study.