Fit After Baby: A Health Intervention to Increase Postpartum Weight Loss in Women at Increased Risk for Cardiometabolic Disease
Status: | Recruiting |
---|---|
Conditions: | High Blood Pressure (Hypertension), Obesity Weight Loss, Peripheral Vascular Disease, Women's Studies, Women's Studies, Diabetes |
Therapuetic Areas: | Cardiology / Vascular Diseases, Endocrinology, Reproductive |
Healthy: | No |
Age Range: | 18 - 45 |
Updated: | 12/29/2018 |
Start Date: | September 1, 2017 |
End Date: | December 31, 2021 |
Contact: | Jacinda Nicklas, MD, MPH, MA |
Email: | jacinda.nicklas@ucdenver.edu |
Phone: | (303)724-9028 |
Fit After Baby: A Randomized Controlled Trial of a Mobile Health Intervention to Increase Postpartum Weight Loss in Women at Increased Risk for Cardiometabolic Disease
This study plans to learn more about how to increase postpartum weight loss and how to
decrease risk factors for postpartum women at increased risk for diabetes and heart disease.
The program is delivered using a mobile application (app) and a lifestyle coach. This mobile
application is developed for women who are at higher risk for diabetes and heart disease.
Women who have gestational diabetes, (diabetes during pregnancy, or GDM), gestational
hypertension (high blood pressure), and/or preeclampsia (high blood pressure and protein in
the urine), and/or small-for gestational-age, and/or preterm (early) delivery during their
pregnancies have a higher risk for diabetes and heart disease. This mobile application was
developed using the latest research studies and using the evidence-based Diabetes Prevention
and Colorado Weigh programs. The goal of the program is to help women lose weight and
participate in physical activity after delivery.
decrease risk factors for postpartum women at increased risk for diabetes and heart disease.
The program is delivered using a mobile application (app) and a lifestyle coach. This mobile
application is developed for women who are at higher risk for diabetes and heart disease.
Women who have gestational diabetes, (diabetes during pregnancy, or GDM), gestational
hypertension (high blood pressure), and/or preeclampsia (high blood pressure and protein in
the urine), and/or small-for gestational-age, and/or preterm (early) delivery during their
pregnancies have a higher risk for diabetes and heart disease. This mobile application was
developed using the latest research studies and using the evidence-based Diabetes Prevention
and Colorado Weigh programs. The goal of the program is to help women lose weight and
participate in physical activity after delivery.
Inclusion Criteria:
1. Age 18-45
2. Postpartum Body Mass Index (BMI): 26- 45 kg/m2 (≥24 for Asians)
3. Positive history of one or more of the following complications in most recent
singleton or twin pregnancy:
1. Gestational diabetes mellitus (by Carpenter-Coustan criteria, IADPSG
(International Association of the Diabetes and Pregnancy Study Groups) criteria,
or a documented clinical diagnosis). Women with a glucose value >200 mg/dL after
a 50-g glucose challenge test at >12 weeks gestation will also be included.
2. Preeclampsia (high blood pressure and proteinuria diagnosed after 20 weeks
gestation)
3. Gestational hypertension (new hypertension diagnosed after 20 weeks without
proteinuria)
4. Pre-term delivery (32-37 weeks)
5. Small for gestational age (<10th percentile for gestational age)
4. Access to and be willing to use a wi-fi enabled iPhone (5 or higher) or iPod (5 or
higher).
5. Capable of providing informed consent
6. Between 4 weeks and 16 weeks after delivery
Exclusion criteria include:
1. Personal history of Type 1 or 2 diabetes
2. Personal history of breast cancer or any other type of cancer other than a basal cell
skin cancer;
3. Personal history of major chronic illness all to be assessed by the study physician
for ability to participate, including:
1. cardiovascular disease (coronary artery disease, congestive heart failure,
valvular heart disease, stroke, transient ischemic attack, or intermittent
claudication),
2. kidney disease affecting kidney function severe enough to affect participation,
3. liver disease affecting liver function severely enough to affect participation,
4. venous or arterial thromboembolic disease,
5. untreated adrenal insufficiency,
6. depression requiring hospitalization within the past 6 months, or
7. non-pregnancy related illness requiring overnight hospitalization in the past 6
months;
4. Underlying disease/treatment that might interfere with participation in/completion of
the study (e.g. significant gastrointestinal conditions, major psychiatric disorders
affecting the ability to participate, and others at the discretion of the study
clinician);
5. Re-current pregnancy;
6. Diagnosis of diseases associated with glucose metabolism;
7. Current or planned participation in a commercial weight loss program (i.e. Jenny
Craig) over the duration of the study;
8. Previous or planned bariatric surgery;
9. Taking certain prescription medications including
1. high dose glucocorticoids,
2. atypical antipsychotics associated with weight gain (such as risperdal
(risperidone), clozapine (clozaril), olanzapine (zyprexa), quetiapine (seroquel),
etc.) or
3. weight loss medications including prescription (Qsymia, phentermine, topiramate,
Belviq, Contrave, Saxenda, Orlistat), or non-prescription (Alli) medications;
10. Taking metformin or other medications known to affect glucose metabolism;
11. Other active medical problems detected by examination or laboratory testing, at the
discretion of the physician;
12. Any fasting blood glucose > 126 mg/dl, any HbA1c at or above 6.5%, or any plasma
glucose >200 mg/dl during the first trimester.
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