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A Mobile Health Intervention to Achieve Appropriate Gestational Weight Gain in Overweight/Obese Women

Not Applicable
Completed
Conditions
Gestational Weight Gain
Interventions
Behavioral: Lifestyle Intervention
Registration Number
NCT03880461
Lead Sponsor
Kaiser Permanente
Brief Summary

The aim of this trial is to investigate the effectiveness of a mobile health (mhealth) intervention to help overweight and obese women achieve appropriate gestational weight gain (GWG) for their pre-pregnancy body mass index (BMI). The goal of the intervention is to help women achieve GWG within the range recommended by the Institute of Medicine. The investigators propose an adaptive intervention that begins with an effective, yet low resource-intensive treatment and then provides incremental support and resources only to patients who need them. The intervention includes: 1) an mHealth tool allowing data to be automatically transmitted to a mobile website; 2) personalized text messages; and 3) personalized 1:1 telephone coaching sessions. The latter more intensive components are reserved for patients whose GWG is not within the IOM guidelines. The lifestyle intervention will be delivered through 1 telephone counseling session with a study dietician trained in motivational interviewing techniques, as well as through technology-based tools, automated text messages and weekly e-mails of core lifestyle intervention sessions. Personalized text messages and 1:1 telephone coaching sessions will be given to those who are not meeting the GWG guidelines. The lifestyle intervention will be compared to usual medical care. Maternal outcomes will be assessed shortly before delivery and at 6 weeks postpartum. Infant birthweight and weight at one year will also be assessed.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
1335
Inclusion Criteria
  • Pregnant
  • Women receiving prenatal care at Kaiser Permanente San Francisco and Oakland and whose obstetric care clinicians consent to participate;
  • Pregravid BMI 25 to <40 (as determined from a measured pregravid weight in electronic medical record);
  • Has access to a smartphone and Wi-Fi;
  • Provides informed consent to participate.
Exclusion Criteria
  • Multiple births;
  • Planning to move out of the area during the study period;
  • Inability to speak, read, or understand English;
  • Placed on bed rest at time of enrollment; ->15 weeks' gestation at enrollment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Lifestyle InterventionLifestyle InterventionThe goal of the intervention is to help women achieve GWG within the range recommended by the Institute of Medicine. The lifestyle intervention will be delivered through 1 telephone counseling session with a study dietician trained in motivational interviewing techniques, as well as through technology-based tools, automated text messages and weekly e-mails of core lifestyle intervention sessions. Personalized text messages and 1:1 telephone coaching sessions will be given to those who are not meeting the GWG guidelines.
Primary Outcome Measures
NameTimeMethod
Total Gestational Weight Gain (GWG)From 10 gestational weeks until time of delivery (duration of up to 9 months)

Calculated as last measured pregnancy weight at the time of delivery minus measured weight at 10 gestational weeks

Rate of Total GWGFrom 10 gestational weeks until time of delivery (duration of up to 9 months)

Calculated as total gestational weight gain / (# of weeks between 10 gestational weeks and the time of delivery)

Proportion of Women Meeting the Institute of Medicine's GWG RecommendationFrom 10 gestational weeks until time of delivery (duration of up to 9 months)

Proportion of women meeting the IOM's GWG recommendation for weekly rate of GWG

Secondary Outcome Measures
NameTimeMethod
Trimester-specific Weekly Rate of GWG0 - 13 gestational weeks; 14 - 26 gestational weeks; 27 - 40 gestational weeks
GWG Trajectory Throughout PregnancyFrom 10 gestational weeks until time of delivery (duration of up to 9 months)
Change in Moderate to Vigorous Physical Activity (in MET Hrs/Week) as Assessed by the Pregnancy Physical Activity Questionnaire (PPAQ)Between 12 weeks and 33 weeks of pregnancy

We will assess change in moderate to vigorous physical activity between study assessments in pregnancy. The sports and exercise domain encompasses 10 PPAQ activities of moderate intensity (ranging 3.2 MET to 6 MET) and 2 PPAQ activities of vigorous intensity (6.5 MET and 7 MET). The volumes of all activities in the sports and exercise domain will be summed to arrive at an estimate of overall volume of moderate to vigorous intensity sports and exercise activity, expressed in MET hours per week. Higher levels of activity are generally associated with better outcomes. The distributions of all physical activity variables will be assessed for outliers.

Overall Diet Quality According to the Healthy Eating Index-2015 (HEI-2015)Assessed at 12 weeks of pregnancy

The HEI-2015 reflects adherence to the 2015-2020 Dietary Guidelines for Americans; it is comprised of 13 components as well as an overall score. The scoring system ranges from 0 to 100, where higher values indicate a better diet quality.

Postpartum Weight RetentionAssessed at 6 weeks postpartum
The Proportion of Infants With Appropriate Birthweight (>10th and <90th Percentile of Sex-, Gestational Age-, and Racial/Ethnic-specific Distribution)Assessed at birth
Infant Growth (BMI Z-score)From birth to 12 months of age

Trial Locations

Locations (4)

Kaiser Permanente Oakland

🇺🇸

Oakland, California, United States

Kaiser Permanente Redwood City

🇺🇸

Redwood City, California, United States

Kaiser Permanente San Francisco

🇺🇸

San Francisco, California, United States

Kaiser Permanente Santa Clara

🇺🇸

Santa Clara, California, United States

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