search
Back to results

The Effect of Vitamin D Supplementation in Overweight and Obese Pregnant Women

Primary Purpose

Overweight and Obesity

Status
Active
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Vitamin D3
Sponsored by
KK Women's and Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Overweight and Obesity focused on measuring Vitamin D supplementation, Lipid profile, Vitamin D status, Birth outcomes, Pregnancy complications

Eligibility Criteria

21 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Gestation ≤16weeks (16 weeks + 6 days) upon intervention
  2. Pre-pregnancy BMI ≥25 kg/m2
  3. Aged 21-45 years
  4. Willing and able to provide written, informed consent

Exclusion Criteria:

  1. Having current or past hypo/hyperparathyroidism, hypercalciuria, hypercalcemia or osteomalacia
  2. History of renal disease (including kidney stones and etc.), liver dysfunction, tuberculosis or sarcoidosis
  3. Pre-existing diabetes mellitus or chronic hypertension
  4. Taking lipid-lowering medicine
  5. Gestational diabetes (as confirmed by oral glucose tolerance test) or gestational hypertensive disorder
  6. Multiple pregnancy

Sites / Locations

  • KK Women's and Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Vitamin D3

Control

Arm Description

The Vitamin D3 (intervention) arm will receive a total of 800 IU vitamin D3 supplementation per day.

The control arm will receive 400 IU vitamin D3 per day from routine antenatal multivitamin supplementation.

Outcomes

Primary Outcome Measures

Change in maternal serum 25OHD concentration
Change in maternal total cholesterol level
Change in maternal HDL-cholesterol level
Change in maternal LDL-cholesterol level
Change in maternal triglyceride level

Secondary Outcome Measures

Incidence of preeclampsia
Incidence of gestational hypertension
Incidence of gestational diabetes
Fasting glucose level
1-hour post-load glucose level
2-hour post-load glucose level
Incidence of caesarean section
Incidence of preterm birth (<37 weeks)
Incidence of low birth weight (<2500g)
Neonatal birth weight (g)
Neonatal birth length (cm)
Neonatal head circumference (cm)
Incidence of admission to special care (including intensive care) during neonatal period

Full Information

First Posted
April 6, 2021
Last Updated
October 4, 2023
Sponsor
KK Women's and Children's Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT04841265
Brief Title
The Effect of Vitamin D Supplementation in Overweight and Obese Pregnant Women
Official Title
The Effect of Vitamin D Supplementation in Overweight and Obese Pregnant Women
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 28, 2021 (Actual)
Primary Completion Date
April 11, 2023 (Actual)
Study Completion Date
March 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
KK Women's and Children's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To understand the role of vitamin D supplementation on pregnancy outcomes and metabolic status in overweight and obese pregnant women.
Detailed Description
The effects of vitamin D supplementation on pregnancy outcomes and metabolic status of overweight and obese pregnant women remain uncertain. In particular, the dosage of vitamin D supplementation has not been defined in this high risk group of women. This study aims to examine whether oral supplement of vitamin D3 (cholecalciferol) in total dosage of 800 IU(prenatal multivitamin containing 400 IU vitamin D3 + 400 IU vitamin D3 alone) given to overweight and obese pregnant women since early pregnancy until delivery can improve maternal and neonatal outcomes, compared with those given prenatal multivitamin containing 400 IU vitamin D3 supplementation, a commonly given antenatal supplement in Singapore. The investigators' hypothesis is that higher dose vitamin D supplementation would lead to better outcomes in overweight and obese pregnant women. The investigators will conduct a two-arm, parallel non-blinded randomized controlled trial. Women with body mass index ≥25kg/m2 will be randomly assigned into groups with a 1:1 randomization ratio, receiving either 800 or 400 IU vitamin D3 supplementation. The study will be conducted at the antenatal clinics, KK Women's and Children's Hospital, Singapore. Measurements of serum 25-hydroxyvitamin D (25OHD), lipid profile and lifestyles information will be taken for all women at baseline (≤16 weeks gestation) and after three months of intervention (26-30 weeks gestation). All women will continue with the vitamin D3 supplementation until delivery. Primary outcomes include levels of maternal serum 25OHDconcentration and lipid profile at 26-30 gestation weeks as compared with the controls, adjusting for baseline measurements. Secondary outcomes include preeclampsia, gestational hypertension, gestational diabetes, glycaemic levels, caesarean section, gestational weight gain, preterm birth, low birth weight and small-for-gestational-age. This study will fill up the gap of knowledge regarding the role of vitamin D supplementation on pregnancy outcomes and metabolic status in overweight and obese pregnant women.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity
Keywords
Vitamin D supplementation, Lipid profile, Vitamin D status, Birth outcomes, Pregnancy complications

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Vitamin D3
Arm Type
Active Comparator
Arm Description
The Vitamin D3 (intervention) arm will receive a total of 800 IU vitamin D3 supplementation per day.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control arm will receive 400 IU vitamin D3 per day from routine antenatal multivitamin supplementation.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Intervention Description
The intervention arm will receive 400 IU vitamin D3 from routine antenatal multivitamin supplement tablet + 400 IU vitamin D3 daily until delivery.
Primary Outcome Measure Information:
Title
Change in maternal serum 25OHD concentration
Time Frame
Baseline, 26-30 gestational weeks
Title
Change in maternal total cholesterol level
Time Frame
Baseline, 26-30 gestational weeks
Title
Change in maternal HDL-cholesterol level
Time Frame
Baseline, 26-30 gestational weeks
Title
Change in maternal LDL-cholesterol level
Time Frame
Baseline, 26-30 gestational weeks
Title
Change in maternal triglyceride level
Time Frame
Baseline, 26-30 gestational weeks
Secondary Outcome Measure Information:
Title
Incidence of preeclampsia
Time Frame
up to delivery
Title
Incidence of gestational hypertension
Time Frame
Through pregnancy until delivery
Title
Incidence of gestational diabetes
Time Frame
Through pregnancy until delivery
Title
Fasting glucose level
Time Frame
24-28 gestational weeks
Title
1-hour post-load glucose level
Time Frame
24-28 gestational weeks
Title
2-hour post-load glucose level
Time Frame
24-28 gestational weeks
Title
Incidence of caesarean section
Time Frame
At delivery
Title
Incidence of preterm birth (<37 weeks)
Time Frame
At delivery
Title
Incidence of low birth weight (<2500g)
Time Frame
At delivery
Title
Neonatal birth weight (g)
Time Frame
At delivery
Title
Neonatal birth length (cm)
Time Frame
At delivery
Title
Neonatal head circumference (cm)
Time Frame
At delivery
Title
Incidence of admission to special care (including intensive care) during neonatal period
Time Frame
Within 28 days after delivery

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Overweight and obese pregnant women
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Gestation ≤16weeks (16 weeks + 6 days) upon intervention Pre-pregnancy BMI ≥25 kg/m2 Aged 21-45 years Willing and able to provide written, informed consent Exclusion Criteria: Having current or past hypo/hyperparathyroidism, hypercalciuria, hypercalcemia or osteomalacia History of renal disease (including kidney stones and etc.), liver dysfunction, tuberculosis or sarcoidosis Pre-existing diabetes mellitus or chronic hypertension Taking lipid-lowering medicine Gestational diabetes (as confirmed by oral glucose tolerance test) or gestational hypertensive disorder Multiple pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Loy See Ling, PhD
Organizational Affiliation
KK Women's and Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
KK Women's and Children's Hospital
City
Singapore
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Effect of Vitamin D Supplementation in Overweight and Obese Pregnant Women

We'll reach out to this number within 24 hrs