CURE-DM: Effect of Low-Calorie Diet and Lifestyle Intervention on Reversal of T2DM

Sponsor
Diabetes Foundation, India (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05925946
Collaborator
Ministry of Science and Technology, India (Other)
60
2
37

Study Details

Study Description

Brief Summary

An increase in body fat, even when within the normal BMI range is one of the essential drivers of T2DM in Asian Indians. In this context, the relationship between excess hepatic fat and pancreatic fat appears to be necessary. A low-calorie (high protein and low carb) vegetarian diet with appropriate exercise, in a protocol similar to the DiRECT study, may lead to weight loss, reversal of diabetes, and decrease in ectopic fat.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: CURE-DM
N/A

Detailed Description

Diabetes is one of the biggest global public health problems. India has 100 million people living with diabetes as per the 2023 data. Reversal of T2DM, the holy grail of diabetes management, was not deemed possible until recently. Primary care-led weight management for remission of type 2 diabetes (DiRECT) trial has been conducted in obese patients with T2DM patients for a period of 2 years in the UK. Research on the effect of dietary intervention would be necessary for Asian Indians since liver fat deposition is more severe than in white Caucasians. Although some nutritionists and physicians are replicating methods of DiRECT study in their patients, it is not clear if similar diets will work effectively in community-dwelling Asian Indians.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Prevention
Official Title:
Effect of Low-Calorie Diet and Lifestyle Intervention on Reversal of Type 2 Diabetes Mellitus, Hepatic and Pancreatic Fat: A Two-year Randomized Control Trial in New Delhi, India
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Sep 30, 2026
Anticipated Study Completion Date :
Oct 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Phase1 (Partial diet replacement) (850 Kcal/day) (12-20 weeks)): Phase 2 (Gradual increase in calories) (20-28 weeks) (1100 Kcal/day): Phase 3 (Weight loss maintenance) (29-104 weeks) (up to 1200Kcal/day) :

Dietary Supplement: CURE-DM
This randomized controlled prospective trial will be of 2 years duration where 150 patients with T2DM from urban areas of Delhi will be screened. These subjects will be randomized into two groups by computer-generated randomization list using variable block size. Group A (n, 60, test group)will be received a low-calorie diet along with appropriate exercise counseling; and group B (n, 60, Control group) will be received balanced diet along with exercise advice.

No Intervention: Control Group

Subjects will be given routine care for diabetes and obesity management with no change in medication. The meal plan for the control group will consist of 1400 Kcal/day achieved through small frequently distributed meals constituting around 15% of protein, 60% of carbohydrates and 25% of fat; with a menu resembling standard Indian dietary patterns and meal combinations.

Outcome Measures

Primary Outcome Measures

  1. Reversal of diabetes [24 Months]

    This randomized controlled prospective trial will be of 2 years duration with T2D. These subjects will be randomized into two groups, Group A (intervention group) will receive a professionally supported low-calorie diet along with appropriate exercise counselling; Group B (Control group) will be receiving encouragement to follow standard diet and exercise advice.

Secondary Outcome Measures

  1. Muscle strength [24 Months]

    Handgrip muscle strength by Jamar Dynamometer

  2. Anthropometric assessment [24 Months]

    Weight, BMI, circumferences (waist, hip, mid-thigh, mid-arm and neck), skinfold thickness (biceps, triceps, sub scapular, supra-iliac, thigh, lateral thoracic and calf)

  3. Hepatic and Pancreatic Fat [24 Months]

    Liver and pancreatic fat fraction (proton-density fat fraction-magnetic resonance imaging (PDFF-MRI) and thigh skeletal muscle area (by MRI).

  4. Body fat [24 Months]

    Body fat will be done by Whole body dual-energy X-ray absorptiometry (DEXA scan

  5. Insulin Resistance [24 Months]

    Surrogate markers of insulin sensitivity

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Diagnosed with T2DM within the previous 3 years

  • Age 20-65 years

  • BMI >25-45kg/m2

  • HbA1c> 6.5% at baseline (on current treatment, if any)

Exclusion criteria:
  • Recent or screening HbA1c of 9% or higher

  • Weight loss of >5 kg within the previous 6 months

  • Significant cardiopulmonary

  • Hepatic, or another endocrine disease

  • Current participation in any other research drug study in the previous three months

  • Past history of bariatric surgery Malignancy other than minor skin lesions and Possibility of pregnancy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Diabetes Foundation, India
  • Ministry of Science and Technology, India

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Diabetes Foundation, India
ClinicalTrials.gov Identifier:
NCT05925946
Other Study ID Numbers:
  • 2022-1312
First Posted:
Jun 29, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Diabetes Foundation, India
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023