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Prevention of Type 2 Diabetes With Vitamin D (PREVENT-WIN)

Primary Purpose

Prediabetes

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

About this trial

This is an interventional prevention trial for Prediabetes

Eligibility Criteria

20 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy women aged 20-60 years.

Exclusion Criteria:

  • Received Vitamin D or calcium supplementation in the previous six months.
  • On any medication within last one month which could potentially influence insulin secretion, insulin sensitivity, vitamin D or calcium metabolism (e.g. metformin, thiazolidenediones, steroids etc.) and on any medication that activate steroid and xenobiotic receptors, and drugs used in transplantation
  • Pregnancy and lactation at time of study
  • Severe end organ damage or chronic diseases: renal/hepatic failure, any malignancy, major systemic illness etc.
  • Known case of HIV infection.
  • Known case of diabetes mellitus and other endocrine disorders.

Sites / Locations

  • Fortis CDOC center of Excellence for Diabetes Obesity and Endocrinoogy, New Delhi, India

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

vitamin D with diet and lifestyle

placebo with diet and lifestyle modification

Arm Description

vitamin D supplementation along with diet and lifestyle modification was given

placebo with diet and lifestyle modification was given

Outcomes

Primary Outcome Measures

fasting glucose (mg/dL)

Secondary Outcome Measures

TC (mg/dL)

Full Information

First Posted
July 29, 2015
Last Updated
June 13, 2023
Sponsor
Diabetes Foundation, India
Collaborators
Ministry of Science and Technology, India
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1. Study Identification

Unique Protocol Identification Number
NCT02513875
Brief Title
Prevention of Type 2 Diabetes With Vitamin D
Acronym
PREVENT-WIN
Official Title
Prevention of Type 2 Diabetes in Women With Prediabetes Using Vitamin D Supplementation and Lifestyle Intervention in North India (PREVENT-WIN Study)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
February 2013 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
January 25, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Diabetes Foundation, India
Collaborators
Ministry of Science and Technology, India

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The work plan will have the following S&T components. Component 1: Cross-sectional Study Cross-sectional study will be of 1.5 years where 400 women from rural will be screened randomly for the vitamin D deficiency and its determinants including duration of sun exposure. Component 2: Prospective Study This open-label randomized placebo-controlled trial would be done in 150 pre-diabetic women with vitamin D deficiency. The women will be recruited from cross-sectional study, out patient department and health camps and they will be followed up for 2 years. The women will be randomized into two groups; lifestyle modification counseling along with intervention with either vitamin D or placebo. The levels of vitamin D and blood glucose will be assessed periodically (every 6 months). In those having recurrent vitamin D deficiency, the course of vitamin D will be repeated. At the end of the study, incidence of T2DM in both groups will be compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetes

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
121 (Actual)

8. Arms, Groups, and Interventions

Arm Title
vitamin D with diet and lifestyle
Arm Type
Experimental
Arm Description
vitamin D supplementation along with diet and lifestyle modification was given
Arm Title
placebo with diet and lifestyle modification
Arm Type
Placebo Comparator
Arm Description
placebo with diet and lifestyle modification was given
Intervention Type
Dietary Supplement
Intervention Name(s)
vitamin D
Intervention Description
60,000 IU per week for 8 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
placebo +diet and lifestyle
Primary Outcome Measure Information:
Title
fasting glucose (mg/dL)
Time Frame
2 years
Secondary Outcome Measure Information:
Title
TC (mg/dL)
Time Frame
2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy women aged 20-60 years. Exclusion Criteria: Received Vitamin D or calcium supplementation in the previous six months. On any medication within last one month which could potentially influence insulin secretion, insulin sensitivity, vitamin D or calcium metabolism (e.g. metformin, thiazolidenediones, steroids etc.) and on any medication that activate steroid and xenobiotic receptors, and drugs used in transplantation Pregnancy and lactation at time of study Severe end organ damage or chronic diseases: renal/hepatic failure, any malignancy, major systemic illness etc. Known case of HIV infection. Known case of diabetes mellitus and other endocrine disorders.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anoop Misra, MD
Organizational Affiliation
Diabetes Foundation, India
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fortis CDOC center of Excellence for Diabetes Obesity and Endocrinoogy, New Delhi, India
City
Delhi
ZIP/Postal Code
110048
Country
India

12. IPD Sharing Statement

Learn more about this trial

Prevention of Type 2 Diabetes With Vitamin D

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