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Bringing NELIP for Obese Pregnant Women Into Clinical Practice

Primary Purpose

Obesity, Pregnancy

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Nutrition Lifestyle Intervention Program (NLIP)
Exercise Lifestyle Intervention Program (ELIP)
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity focused on measuring Obesity prevention, Nutrition and exercise in pregnancy, Postpartum, Maternal obesity risk

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient referred to "My Clinic" at London Health Sciences Centre
  • 18 or older
  • 12-20 weeks gestational age
  • Pre-pregnancy BMI >= 35kg/m2
  • Willing to be randomized

Exclusion Criteria:

  • Contraindication to walking regularly

Sites / Locations

  • University of Western Ontario, London Health Sciences CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

Full NELIP group

Exercise program only/ELIP

Nutrition program only/NLIP

Control

Arm Description

These women (n=10) will receive the full NELIP intervention and will be introduced to both the dietary program and the exercise program as described above under "detailed description".

These women (n=10) will only be given the exercise component (ELIP) of NELIP, as outlined below in interventions. Once dietary intake has been assessed, this group will not be given any dietary intervention but will be encouraged to eat a healthy, balanced diet. Access to the nutritionist in the clinic is available and encouraged.

These women (n=10) will only be given the nutrition program (NLIP) of NELIP as outlined below in intervention. They will be encouraged to be more active but will not be given an exercise intervention.

A control group (n=30) of obese pregnant women will also be recruited and will be matched by pre-pregnancy BMI, maternal age and parity, with no intervention, but will attend the clinic for standard obstetric care and follow-up.

Outcomes

Primary Outcome Measures

Weight gain in pregnancy
Average weekly weight gain and total weight gained throughout pregnancy; recorded from initial recruitment (12-20 weeks GA) to date of delivery (up to 42 weeks). This would include approximately 20 weeks on average of follow-up in the clinic, but up to a maximum of 30 weeks total. Women are assessed at 6 months post partum and weight change measured also.

Secondary Outcome Measures

Infant birth weight
This outcome is measured in grams. Follow-up for infants is also at 6 months of age.
Neonatal morphometrics
Includes infant birth weight:length ratio, infant BMI, newborn skinfolds, and circumferences as described prior
Birth complications
Breast feeding
Maternal weight retention
See above description on weight gain. Analysis will be done and weight gain, retention divided into appropriate groups.
Infant growth
Infant growth will be done in grams and plotted on growth charts, based upon corrected gestational age at birth.

Full Information

First Posted
October 11, 2013
Last Updated
May 10, 2017
Sponsor
Lawson Health Research Institute
Collaborators
Children's National Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02155751
Brief Title
Bringing NELIP for Obese Pregnant Women Into Clinical Practice
Official Title
Bringing an Evidence-based Nutrition and Exercise Lifestyle Intervention Program (NELIP) for Obese Pregnant Women Into Clinical Practice
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (Actual)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lawson Health Research Institute
Collaborators
Children's National Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a pilot project in which investigators will recruit obese (pre-pregnancy BMI of ≥ 35 kg/m2) women from the newly developed "My Clinic" at London Health Sciences Centre as well as normal obstetrical care at London Health Sciences Centre. Patients will be randomized to one of three treatment groups: 1) the full Nutrition and Exercise Lifestyle Intervention Program (NELIP), 2) Nutrition program only, or 3) Exercise program only. The investigators hypothesize that the evidence-based NELIP for obese pregnant women will be feasible to adopt in a clinical setting and will prevent excessive gestational weight gain, gestational diabetes and promote healthy infant growth patterns at the 6 and 12 month milestones. Outcomes may be improved in My Clinic over normal obstetrical care patients with interprofessional services.
Detailed Description
Thirty pregnant women (12-16 weeks gestation) with a pre-pregnancy BMI of ≥35 kg/m2 will be recruited from "My Clinic" and normal obstetrical care. "My Clinic" is a new outpatient obstetrical care clinic being initiated at London Health Sciences Centre for obese women. Women in early pregnancy (12-16 weeks) will be recruited through family physicians' offices from Southwest Ontario to participate in "My Clinic" if their BMI is > or = 35 at the initiation of pregnancy. The clinic will integrate various professional groups currently fractured in their provision of care, including ultrasound, nutrition, social work and obstetrical care to assess and provide care for this group of women, while providing the patients a group atmosphere for regular counselling during their scheduled antenatal visits. The clinic will also offer group counseling sessions for patients covering various topics relating to lifestyle choices including diet and exercise. Each woman will be screened for medical comorbidities of obesity, including blood pressure measurements and a fasting oral glucose tolerance test to screen for gestational diabetes. Once medically pre-screened with no contraindications to walking regularly, each woman will be approached by a member of the research team. Each woman will record for 3 consecutive days (including one weekend day) a food intake diary and also record the number of steps taken during that same time period, using a pedometer with instructions on how to wear it and record her daily steps. Once these have been returned, the women will be randomized into one of three groups by computer generated model. The order of randomization will be kept in the clinic in opaque envelopes and selected by the research assistant after inclusion in the study is confirmed. The three groups are as described; The NELIP group (N=10) with full intervention (1) will be introduced to a walking program in which they walk for 25 minutes, 3 to 4 times per week, adding 2 minutes each week, until 40 minutes is reached and then maintained until delivery. Each woman will be given a pedometer and log sheet to keep track of daily steps and to initiate self-monitoring behaviour. The dietary program will mimic the gestational diabetic meal plan: a) individualize total energy intake with a minimum of 2000 kcal/day (8360 kilojoule/day), taking into account the usual energy intake as indicated by each dietary assessment (including 3-day food intake records) with a restriction of not more than 33% total energy intake; b) adjust if necessary the total carbohydrate intake to 40-50% of total energy intake, distributing carbohydrate intake throughout the day with three balanced meals, and three snacks per day emphasizing complex carbohydrates and low glycemic index foods; c) adjust the total fat intake to 30% of total energy intake (substituting monounsaturated fatty acids for saturated and trans-fatty acids), with the remaining 30% dedicated to protein intake; and d) meet all micronutrient and fluid needs recommended during pregnancy (2). In order to tease out the effectiveness of the full NELIP, the second group (N=10) will only be given the exercise component (ELIP) of NELIP. Once dietary intake has been assessed, this group will not be given any dietary intervention but will be encouraged to eat a healthy, balanced diet. The third group (N=10) will only be given the nutrition program (NLIP) of NELIP. They will be encouraged to be more active but will not be given an exercise intervention. A control group (N=30) will also be recruited from the "My Clinic" and other women undergoing care through the obstetrical program at London Health Sciences Centre. The women will be matched by pre-pregnancy BMI, maternal age and parity, with no intervention, but will attend the clinic for standard obstetric care and follow-up. Women in groups 1-3 will have weekly weight gain recorded until delivery. Infant gender, body weight, length, neonatal morphometrics (birth weight:length ratio, BMI, newborn skinfolds, and circumferences) and placental weight (placenta:birth weight ratio) will be recorded in all women within 6-18 hours of birth. Any interventions or complications at birth will also be recorded. At 6 and 12 months post partum, all maternal-infant pairs (including controls) will be invited to return to the clinic for follow-up. Breast feeding status, maternal weight retention, infant weight/length/BMI/skinfolds/girths and growth patterns will be assessed and compared to the WHO Child Growth Standards for infants based on gender (see above). All women will complete the Kaiser Physical Activity Questionnaire at entry, 34-36 weeks of gestation and at each follow-up appointment to track changes in physical activity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Pregnancy
Keywords
Obesity prevention, Nutrition and exercise in pregnancy, Postpartum, Maternal obesity risk

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
23 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Full NELIP group
Arm Type
Experimental
Arm Description
These women (n=10) will receive the full NELIP intervention and will be introduced to both the dietary program and the exercise program as described above under "detailed description".
Arm Title
Exercise program only/ELIP
Arm Type
Experimental
Arm Description
These women (n=10) will only be given the exercise component (ELIP) of NELIP, as outlined below in interventions. Once dietary intake has been assessed, this group will not be given any dietary intervention but will be encouraged to eat a healthy, balanced diet. Access to the nutritionist in the clinic is available and encouraged.
Arm Title
Nutrition program only/NLIP
Arm Type
Experimental
Arm Description
These women (n=10) will only be given the nutrition program (NLIP) of NELIP as outlined below in intervention. They will be encouraged to be more active but will not be given an exercise intervention.
Arm Title
Control
Arm Type
No Intervention
Arm Description
A control group (n=30) of obese pregnant women will also be recruited and will be matched by pre-pregnancy BMI, maternal age and parity, with no intervention, but will attend the clinic for standard obstetric care and follow-up.
Intervention Type
Behavioral
Intervention Name(s)
Nutrition Lifestyle Intervention Program (NLIP)
Intervention Description
The dietary program will mimic the gestational diabetic meal plan: a) individualize total energy intake with a minimum of 2000 kcal/day (8360 kJ/day), taking into account the usual energy intake as indicated by each dietary assessment (including 3-day food intake records) with a restriction of not more than 33% total energy intake; b) adjust if necessary the total carbohydrate intake to 40-50% of total energy intake, distributing carbohydrate intake throughout the day with three balanced meals, and three snacks per day emphasizing complex carbohydrates and low glycemic index foods; c) adjust the total fat intake to 30% of total energy intake (substituting monounsaturated fatty acids for saturated and trans-fatty acids), with the remaining 30% dedicated to protein intake; and d) meet all micronutrient and fluid needs recommended during pregnancy.
Intervention Type
Behavioral
Intervention Name(s)
Exercise Lifestyle Intervention Program (ELIP)
Intervention Description
The exercise program includes a walking program in which pregnant women walk for 25 minutes, 3 to 4 times per week, adding 2 minutes each week, until 40 minutes is reached and then maintained until delivery. Each woman will be given a pedometer and log sheet to keep track of daily steps and to initiate self-monitoring behaviour.
Primary Outcome Measure Information:
Title
Weight gain in pregnancy
Description
Average weekly weight gain and total weight gained throughout pregnancy; recorded from initial recruitment (12-20 weeks GA) to date of delivery (up to 42 weeks). This would include approximately 20 weeks on average of follow-up in the clinic, but up to a maximum of 30 weeks total. Women are assessed at 6 months post partum and weight change measured also.
Time Frame
up to 42 weeks
Secondary Outcome Measure Information:
Title
Infant birth weight
Description
This outcome is measured in grams. Follow-up for infants is also at 6 months of age.
Time Frame
Measured at time of birth
Title
Neonatal morphometrics
Description
Includes infant birth weight:length ratio, infant BMI, newborn skinfolds, and circumferences as described prior
Time Frame
Measured at birth, 6 months postpartum, 12 months postpartum
Title
Birth complications
Time Frame
Measured at time of birth
Title
Breast feeding
Time Frame
Measured at birth, 6 months postpartum, 12 months postpartum
Title
Maternal weight retention
Description
See above description on weight gain. Analysis will be done and weight gain, retention divided into appropriate groups.
Time Frame
Measured at 6 and 12 months postpartum
Title
Infant growth
Description
Infant growth will be done in grams and plotted on growth charts, based upon corrected gestational age at birth.
Time Frame
Measured at 6 and 12 months postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient referred to "My Clinic" at London Health Sciences Centre 18 or older 12-20 weeks gestational age Pre-pregnancy BMI >= 35kg/m2 Willing to be randomized Exclusion Criteria: Contraindication to walking regularly
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Debbie A Penava, MD
Phone
519-646-6401
Email
Debbie.Penava@lhsc.on.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Michelle Mottola, PhD
Phone
519-661-2111
Ext
85480
Email
mmottola@uwo.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Debbie A Penava, MD
Organizational Affiliation
London Health Sciences Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michelle Mottola, PhD
Organizational Affiliation
Western University, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Western Ontario, London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Debbie A Penava, MD
First Name & Middle Initial & Last Name & Degree
Michelle Mottola, PhD
First Name & Middle Initial & Last Name & Degree
Barbra deVrijer, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
20083959
Citation
Mottola MF, Giroux I, Gratton R, Hammond JA, Hanley A, Harris S, McManus R, Davenport MH, Sopper MM. Nutrition and exercise prevent excess weight gain in overweight pregnant women. Med Sci Sports Exerc. 2010 Feb;42(2):265-72. doi: 10.1249/MSS.0b013e3181b5419a.
Results Reference
background
Citation
Health Canada. Nutrition for a health pregnancy: National guidelines for the childbearing years. Ottawa (ON): Minister of Public Works & Government Services Canada (CA); 2010.
Results Reference
background

Learn more about this trial

Bringing NELIP for Obese Pregnant Women Into Clinical Practice

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