Promoting Healthy Weight Gain During Pregnancy
Primary Purpose
Weight Gain
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Lifestyle
Sponsored by
About this trial
This is an interventional treatment trial for Weight Gain focused on measuring Excessive gestational weight gain
Eligibility Criteria
Inclusion Criteria:
- non-smoking, adults,
- < 16 weeks gestation
Exclusion Criteria:
- medical comorbidities
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
control
Intervention
Arm Description
Lifestyle intervention delivered during pregnancy
Outcomes
Primary Outcome Measures
Percentage of women above the Institute of Medicine Guidelines for gestational weight gain
Objective measures of weight collected by trained staff on calibrated scales at study entry and after delivery to classify women as above or below the Institute of Medicine Guidelines for gestational weight gain
Secondary Outcome Measures
Behavioral measures
The Block Food Frequency questionnaire and Paffenbarger physical activity questionnaire will be used to assess diet and exercise behavior.
Full Information
NCT ID
NCT01117961
First Posted
April 15, 2010
Last Updated
April 30, 2013
Sponsor
The Miriam Hospital
Collaborators
California Polytechnic State University-San Luis Obispo, Women and Infants Hospital of Rhode Island, University of California, Berkeley
1. Study Identification
Unique Protocol Identification Number
NCT01117961
Brief Title
Promoting Healthy Weight Gain During Pregnancy
Official Title
Promoting Healthy Weight Gain During Pregnancy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Miriam Hospital
Collaborators
California Polytechnic State University-San Luis Obispo, Women and Infants Hospital of Rhode Island, University of California, Berkeley
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study goal is to determine whether behavioral lifestyle intervention during pregnancy can reduce the number of women who exceed the Institute of Medicine recommendations for weight gain during pregnancy.
It is hypothesized that the intervention will reduce the number of women who exceed weight gain guidelines relative to standard care. The investigators also expect the intervention to reduce the proportion of women exceeding weight gain guidelines in both normal weight and overweight groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Gain
Keywords
Excessive gestational weight gain
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
401 (Actual)
8. Arms, Groups, and Interventions
Arm Title
control
Arm Type
No Intervention
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Lifestyle intervention delivered during pregnancy
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle
Intervention Description
Behavioral lifestyle intervention targeting diet and physical activity to reduce excessive gestational weight gain
Primary Outcome Measure Information:
Title
Percentage of women above the Institute of Medicine Guidelines for gestational weight gain
Description
Objective measures of weight collected by trained staff on calibrated scales at study entry and after delivery to classify women as above or below the Institute of Medicine Guidelines for gestational weight gain
Time Frame
40 weeks
Secondary Outcome Measure Information:
Title
Behavioral measures
Description
The Block Food Frequency questionnaire and Paffenbarger physical activity questionnaire will be used to assess diet and exercise behavior.
Time Frame
40 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
non-smoking, adults,
< 16 weeks gestation
Exclusion Criteria:
medical comorbidities
12. IPD Sharing Statement
Citations:
PubMed Identifier
28525293
Citation
Mercado A, Marquez B, Abrams B, Phipps MG, Wing RR, Phelan S. Where Do Women Get Advice About Weight, Eating, and Physical Activity During Pregnancy? J Womens Health (Larchmt). 2017 Sep;26(9):951-956. doi: 10.1089/jwh.2016.6078. Epub 2017 May 19.
Results Reference
derived
PubMed Identifier
24284438
Citation
Phelan S, Phipps MG, Abrams B, Darroch F, Grantham K, Schaffner A, Wing RR. Does behavioral intervention in pregnancy reduce postpartum weight retention? Twelve-month outcomes of the Fit for Delivery randomized trial. Am J Clin Nutr. 2014 Feb;99(2):302-11. doi: 10.3945/ajcn.113.070151. Epub 2013 Nov 27.
Results Reference
derived
PubMed Identifier
21310836
Citation
Phelan S, Phipps MG, Abrams B, Darroch F, Schaffner A, Wing RR. Randomized trial of a behavioral intervention to prevent excessive gestational weight gain: the Fit for Delivery Study. Am J Clin Nutr. 2011 Apr;93(4):772-9. doi: 10.3945/ajcn.110.005306. Epub 2011 Feb 10.
Results Reference
derived
Learn more about this trial
Promoting Healthy Weight Gain During Pregnancy
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