Access to Nutritional Services and the Effect on Maternal Weight Gain

NCT ID: NCT01713712

Last Updated: 2013-04-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-12-31

Study Completion Date

2014-02-28

Brief Summary

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The purpose of this study is to evaluate the effect of access to nutrition services on pregnancy outcomes in the obese urban population. There are many studies that have shown that obesity has a negative impact on pregnancy. However, currently there are only a few small studies that specifically look at ease of access to nutrition services in an obese urban population and the effect this has on maternal weight gain and pregnancy outcomes. This study will compare two groups of pregnant women with a BMI of 30 or greater. The investigators hypothesize that access to nutritional services will lead to decreased weight gain during pregnancy and improved pregnancy outcomes.

Detailed Description

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The purpose of this study is to evaluate the effect of access to nutrition services on pregnancy outcomes in the obese urban population. Approximately one fourth of women in the United States are overweight and nearly one third are considered to be obese. Pregnancy places obese women at increased risk for several adverse events in the antepartum, intrapartum, and postpartum period. There are many studies that have shown that obesity in pregnancy has a negative impact on pregnancy. However, currently there are few studies in the United States that specifically look at ease of access to nutrition services in an obese urban population and the effect this has on pregnancy outcomes. This study will be a randomized controlled study that will compare two groups of pregnant women with a BMI of 30 or greater one of which has access to nutritional services along with routine prenatal care while the other gets only routine prenatal care. The investigators hypothesize that the obese parturient who has access to nutritional services will have decreased weight gain during pregnancy and ultimately have improved pregnancy outcomes. This will help to guide future care for the obese parturient in the urban population who may have limited access to services.

Conditions

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Pregnancy Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Routine Obstetric Care

Group Type NO_INTERVENTION

No interventions assigned to this group

Nutritional Counseling

Patients will receive an initial 90 minute nutritional consult followed by 60 minute follow up consults every 2 weeks to monitor weight gain and nutritional status.

Group Type EXPERIMENTAL

Nutritional Counseling

Intervention Type BEHAVIORAL

Patients will keep a daily diary of nutritional intake as well as physical activity. They will also follow up with the nutritional counselor six weeks postpartum.

Interventions

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Nutritional Counseling

Patients will keep a daily diary of nutritional intake as well as physical activity. They will also follow up with the nutritional counselor six weeks postpartum.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* primigravid women
* age 19-40yrs
* less than or equal to 18 weeks gestation at time of enrollment
* body mass index (BMI) greater than or equal to 30

Exclusion Criteria

* multiparous women
* less than 19 yrs of age or older than 40
* greater than 18 weeks gestation at time of enrollment
* body mass index (BMI) less than 30
* any significant past medical history including hypertension, diabetes, renal disease, coagulopathy
* past surgical history of gastric bypass/weight loss surgery
Minimum Eligible Age

19 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Abington Memorial Hospital

OTHER

Sponsor Role lead

Responsible Party

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Erin M. Murphy, MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Erin M Murphy, MD

Role: PRINCIPAL_INVESTIGATOR

Abington Memorial Hospital

Bethany Perry, MD

Role: STUDY_DIRECTOR

Abington Memorial Hospital

Locations

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Abington Memorial Hospital

Abington, Pennsylvania, United States

Site Status RECRUITING

Abington Memorial Hospital

Abington, Pennsylvania, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Erin M Murphy, MD

Role: CONTACT

215-481-4211

Bethany Perry, MD

Role: CONTACT

215-481-4211

Facility Contacts

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Erin M Murphy, MD

Role: primary

215-481-4020

Bethany Perry, MD

Role: backup

215-481-4020

Other Identifiers

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11-070

Identifier Type: -

Identifier Source: org_study_id

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