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Pre-meal Load of Raw Almonds and Postprandial Hyperglycemia

Primary Purpose

Intervention

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
almonds
Sponsored by
Diabetes Foundation, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Intervention focused on measuring almonds, Asian Indians, Prediabetes

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Age 18 to 60 years Prediabetes as diagnosed on oral glucose tolerance test (OGTT): Fasting blood glucose ≥100mg/dl and <126 mg/dl and 2-h plasma glucose ≥140mg/dl and <200mg/dl (after ingestion of 75 gram anhydrous oral glucose) or 2-h plasma glucose ≥140mg/dl and <200mg/dl alone.

Exclusion Criteria:

Acute infections and advanced end-organ damage History of hepatitis or pancreatitis, abnormal liver and renal functions Recent (<3 months) changes in weight (≥5%) and/or weight changing medications Any known allergy to nuts uncontrolled hypertension or hypothyroidism suffering from acute infection or any debilitating disease or with renal failure

Sites / Locations

  • Anoop misra

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

treatment

control

Arm Description

premeal load of almonds

standard diet

Outcomes

Primary Outcome Measures

Postprandial blood glucose levels [AUC 0-2 hrs on oral glucose tolerance test (OGTT)]

Secondary Outcome Measures

postprandial blood glucose levels [AUC 0-4 hrs on continuous glucose monitoring system{CGMS}]
Postprandial hyperglycaemia (blood glucose levels 2 hrs post OGTT)

Full Information

First Posted
February 22, 2021
Last Updated
February 18, 2023
Sponsor
Diabetes Foundation, India
Collaborators
National Diabetes Obesity and Cholesterol Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04769726
Brief Title
Pre-meal Load of Raw Almonds and Postprandial Hyperglycemia
Official Title
Evaluation of Pre-meal Load of Raw Almonds on Postprandial Hyperglycemia and Other Metabolic Responses in Asian Indians With Prediabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
December 16, 2017 (Actual)
Primary Completion Date
June 20, 2021 (Actual)
Study Completion Date
June 20, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Diabetes Foundation, India
Collaborators
National Diabetes Obesity and Cholesterol Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
A few studies show the effect of almonds on postprandial hyperglycemia (PPHG); high blood glucose after meals. In our previous study on intervention with almonds, we observed a significant decrease in HbA1C and a small decrease in fasting blood glucose indicating a possible effect of almonds on PPHG. Studies have shown that a preload of a food article that is high in protein, mono-unsaturated fatty acids, fiber, and low in carbohydrates, such as almonds could be helpful in stimulating insulin secretion and help improve postprandial hyperglycemia. The proposed study shall be undertaken to assess the effect of almond supplementation on postprandial hyperglycemia in Asian Indians with prediabetes.
Detailed Description
Acute Phase Study: Randomized controlled cross over study design Number of arms: 2, almond and control, n=60 needed (30 in each arm) Subjects randomized to almonds arm are given a preload of 20 g of almonds 30 minutes prior to ingestion of 75 g of glucose, while those in the control arm do not have any food/almonds before OGTT. Blood samples are collected at (minutes): -30, 30, 0, 30, 60, 90 and 120. Cross over of these subjects is done and OGTT repeated in a similar manner. Assessment of blood glucose, serum insulin, glucagon, C-peptide, serum triglycerides, free fatty acids, DPP-IV, and GLP1 levels are done at these time points. Sub-Acute Study: Three-day almond preload study monitored with CGMS, n=60 needed. All study participants undergoing OGTT are further studied with CGMS for three days each and then crossed over. Those in almonds arm continue to receive preload of almonds (20g almonds, 30 minutes before breakfast, lunch and dinner)for three days and then studied without almond preload after cross over. A washout period of 7 days separates cross-over period. o Chronic Phase Study: Ninety days almond preload study monitored with self-monitoring of blood glucose; n=60 needed. This is a randomized controlled parallel-arm study to evaluate the long-term effect of preload of almonds on hyperglycemia. Subjects fulfilling the inclusion/exclusion criteria are randomized to either the control arm or the almond arm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intervention
Keywords
almonds, Asian Indians, Prediabetes

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
treatment
Arm Type
Experimental
Arm Description
premeal load of almonds
Arm Title
control
Arm Type
No Intervention
Arm Description
standard diet
Intervention Type
Dietary Supplement
Intervention Name(s)
almonds
Intervention Description
almond intervention (20 g) before three major meals (60g per day) for 3 days in subacute phase, before OGTT in the acute phase ad for 3 months in chronic phase
Primary Outcome Measure Information:
Title
Postprandial blood glucose levels [AUC 0-2 hrs on oral glucose tolerance test (OGTT)]
Time Frame
8 days
Secondary Outcome Measure Information:
Title
postprandial blood glucose levels [AUC 0-4 hrs on continuous glucose monitoring system{CGMS}]
Time Frame
15 days
Title
Postprandial hyperglycaemia (blood glucose levels 2 hrs post OGTT)
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 to 60 years Prediabetes as diagnosed on oral glucose tolerance test (OGTT): Fasting blood glucose ≥100mg/dl and <126 mg/dl and 2-h plasma glucose ≥140mg/dl and <200mg/dl (after ingestion of 75 gram anhydrous oral glucose) or 2-h plasma glucose 140mg/dl and <200mg/dl alone. Exclusion Criteria: Acute infections and advanced end-organ damage History of hepatitis or pancreatitis, abnormal liver and renal functions Recent (<3 months) changes in weight (≥5%) and/or weight changing medications Any known allergy to nuts uncontrolled hypertension or hypothyroidism suffering from acute infection or any debilitating disease or with renal failure
Facility Information:
Facility Name
Anoop misra
City
New Delhi
Country
India

12. IPD Sharing Statement

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Pre-meal Load of Raw Almonds and Postprandial Hyperglycemia

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