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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02142452
Other study ID # 28810
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2014
Est. completion date March 2016

Study information

Verified date March 2021
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators will test the efficacy of a tailored behavioral lifestyle modification program to support cardiovascular health in postpartum women with excessive gestational weight gain. This program will include a mobile health texting component postpartum to support changes in nutrition and physical activity. The investigators will randomize women into either the control arm (usual care) or the intervention (usual care + mobile health program postpartum). The women will be recruited during their 3rd trimester once they have been identified as gaining too much weight according to the 2009 IOM guidelines during pregnancy.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Pregnant woman diagnosed with excessive gestational weight at 24 weeks gestation or later - Age 18 years or older - English-speaking, and willing and able to participate in the proposed intervention. Exclusion Criteria: - Inability to provide informed consent and/or an inability to speak, read, or understand English - Primary residence is outside of the immediate catchment area of 10 miles - Physical or mental challenges that precludes them from exercising or returning for scheduled study follow ups - Concurrent enrollment in another behavior modification program

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
behavioral intervention
Behavioral intervention will include a group class for women in their 3rd trimester followed by a mobile texting program to support behavior change postpartum.
Other:
Usual Prenatal Care


Locations

Country Name City State
United States Stanford Hospital and Clinics Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary BMI (body mass index) A mobile Health intervention tailored for the 30 postpartum mother and grounded in behavioral change theory will be associated with significantly more reduction in BMI than 30 women not enrolled in the intervention. 4 months postpartum
Secondary Cardiovascular health metrics (1) Examine changes in cardiovascular health metrics (fasting glucose, fasting insulin, and BP) and markers of inflammation (hs-CRP) verses control group (2) We will evaluate changes in perceived nutrition, physical activity, and weight-loss self-efficacy; self-efficacy has been shown to be a direct predictor of behavior (3) measure the effects of breastfeeding support on the length of time a mother breastfeeds verse the control group. 4 months postpartum
Secondary Change in self efficacy score based on behavioral self-efficacy scale We will measure changes in pre- and post-intervention self-efficacy of all women in intervention and control arms. 4 months postpartum
Secondary Cardiovascular health metrics We will evaluate changes in perceived nutrition, physical activity, and weight-loss self-efficacy; self-efficacy has been shown to be a direct predictor of behavior 4 months postpartum
Secondary Cardiovascular health metric Measure the effects of breastfeeding support on the length of time a mother breastfeeds verse the control group. 4 months postpartum
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