Study Results
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Basic Information
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COMPLETED
420 participants
OBSERVATIONAL
2006-07-31
2006-11-30
Brief Summary
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Our study population will consist of all women over the age 18 who delivered a term infant either by vaginal delivery or cesarean section at Tulsa Regional Medical Center between July 1st 2004 and December 31st 2005.
The diagnosis of obesity will be based upon a Body Mass Index (weight in kilograms/height in meters squared) of thirty or greater. We will look at the infant birth weight as recorded in the patient's chart. We will define SGA or IUGR as birth weight less than the 10th percentile for gestational age as defined previously. The control group will consist of women meeting the same criteria except they will have a BMI less than thirty but greater than 19.8 as low maternal weight is also a risk factor for IUGR. We will compare the average birth weight and the rates of SGA/IUGR infants between the two groups and analyze using the chi-squared method of analysis.
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Detailed Description
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Study Population Inclusion/Exclusion Criteria Our study population will consist of all women over the age 18 who delivered a term infant either by vaginal delivery or cesarean section at Tulsa Regional Medical Center between July 1st 2004 and December 31st 2005. We choose this time frame as we feel this will give an adequate sample size of approximately about 160 women in the study group and about 260 in the control group, while allowing for completion of the project within 12 to 18 months. Our statistician, Dr. Mark Payton, has completed a power analysis for these numbers, and it is included with our submission. We will define a term infant as 37 weeks gestation or greater. They must have had at least one visit at the Houston Park Ob-Gyn clinic, not including the initial prenatal lab visit, before delivery. Our study population will consist of mainly Medicaid patients, most of who are of lower socioeconomic status. The ethnic blend of our study population will include Caucasian, African-American, Hispanic, American Indian, and Asian women. Our study population will have a BMI greater than or equal to 30 based on initial recorded weight and recorded height. We will exclude women with multiple gestation, hypothyroidism, hyperthyroidism, heart disease, tobacco or drug use, gestational or preexisting diabetes, autoimmune disease of any form, hypertension, collagen vascular disease, any disease process resulting in decreased gastrointestinal nutrient absorption, or lung disease as these are conditions known to be risk factors for IUGR (5).
Early Termination Criteria N/A
Methods/Procedures Diagnosis The diagnosis of obesity will be based upon initial weight and height recorded in the patients chart, typically during the first trimester, to derive a BMI (weight in kilograms/height in meters squared). Although total weight gain during a term pregnancy could add enough to the BMI to falsely indicate obesity, since we will be using the initial weight recorded, this difficulty should be minimized. The cutoff for our study group will be a BMI of thirty or greater as this is the definition of obesity by the World Health Organization and the National Institutes of Health. We will look at the infant birth weight as recorded in the patient's chart. We will define SGA or IUGR as birth weight less than the 10th percentile for gestational age as defined previously. The control group will consist of women meeting the same criteria except they will have a BMI less than thirty but greater than 19.8 as low maternal weight is also a risk factor for IUGR.
Data Collection The collaborating investigators and research assistants will collect only the following information from the patients chart: age, height, weight at initial visit, date of delivery, infant birth weight, smoking status, and any of the abovementioned comorbidities that would exclude the patient from the study. No other data will be collected from any patients chart. We will utilize research assistants in the collection of this data, and these research assistants will be OSU medical students employed by the work study program to work on this project. They will be collecting data from clinic records. They have basic human research and HIPAA training and are allowed access to patient chart information as they fall under the OSU community of individuals with this privilege. Analysis We will compare the average birth weight and the rates of SGA/IUGR infants between the two groups. We will analyze the results using chi-squared method of analysis.
Confidentiality The clinic records to be reviewed will be kept in the Houston Park medical records department which is either locked or under security supervision at all times. The hospital records will be kept in the Tulsa Regional Medical Center health information management department. This department is locked 24 hours a day. No identifying information from any individual's chart will be recorded, so de-identification will occur when the data is collected, and no master list of patient names or other identifying information will be kept.
Conditions
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Study Design
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RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
50 Years
FEMALE
Yes
Sponsors
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Oklahoma State University Center for Health Sciences
OTHER
Principal Investigators
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Kimberly A. Sorensen, D.O.
Role: PRINCIPAL_INVESTIGATOR
Oklahoma State University Center for Health Sciences
Locations
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Oklahoma State University Center for Health Sciences Houston Parke Clinic
Tulsa, Oklahoma, United States
Countries
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References
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Hulsey TC, Neal D, Bondo SC, Hulsey T, Newman R. Maternal prepregnant body mass index and weight gain related to low birth weight in South Carolina. South Med J. 2005 Apr;98(4):411-5. doi: 10.1097/01.SMJ.0000145283.69631.FC.
Other Identifiers
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2006017
Identifier Type: -
Identifier Source: org_study_id
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