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Clinical Trials/NCT04131023
NCT04131023
Completed
Not Applicable

Metabolic Tracking During Pregnancy to Promote Adequate Gestational Weight Gain

Arizona State University1 site in 1 country34 target enrollmentSeptember 17, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gestational Weight Gain
Sponsor
Arizona State University
Enrollment
34
Locations
1
Primary Endpoint
Change in Gestational Weight Gain
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

In this study, the investigators aimed to have pregnant women use a hand-held device to track increases in daily caloric needs during pregnancy. Weight gain was assessed over time with the goal of reducing excessive gestational weight gain relative to a group of pregnant women who received standard prenatal care.

Detailed Description

Specific Aims The investigators pursued the following specific aims: 1. Evaluate the impact of a mobile, real-time metabolism tracking device on gestational weight gain (GWG) (i.e. total weight gain and rate of weight gain) in pregnant women. The investigators postulated that the metabolism tracking (Breezing) group would have a higher proportion of women who gain the appropriate amount of weight per IOM recommendations. Further, the investigators expected the women in the Breezing group to gain a mean weight within +/- 3 lbs of their recommended GWG range per IOM guidelines, compared to standard care-receiving controls. 2. Assess changes in resting energy expenditure during pregnancy in relation to self-reported dietary intake (at baseline, 4 weeks, 8 weeks, and 12 weeks). The investigators hypothesized that energy requirements would change across the second trimester and that self-reported caloric intakes would correlate with resting energy expenditure (REE)-corrected values (from Breezing) for women in the Breezing group. Exploratory Aims 1. Evaluate the associations among objective and self-reported sleep parameters (actigraphic total sleep time, sleep onset latency, wake after sleep onset, and mid-sleep point; sleep diary total sleep time, sleep onset latency, wake after sleep onset, and mid-sleep point; insomnia symptoms; and sleep disordered breathing risk) and GWG within the Breezing and control groups.

Registry
clinicaltrials.gov
Start Date
September 17, 2017
End Date
November 1, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Corrie Whisner

Assistant Professor

Arizona State University

Eligibility Criteria

Inclusion Criteria

  • All English and Spanish-speaking, pregnant women
  • Gestational age \< 17 weeks at time of recruitment
  • Aged 18 years or older

Exclusion Criteria

  • High-risk pregnancies that include the following diseases or conditions: fetal growth problems, medical history of hypertension, gastrointestinal disorders, malabsorptive diseases, hyper or hypo-parathyroid conditions, HIV, diabetes (Types 1 and 2 or gestational diabetes), asthma/lung disease, cardiac disease or conditions, current smoker (i.e. women who have smoked 100 cigarettes in their lifetime and now smoke every day or some days) history of eating disorder, or other metabolic conditions known to affect maternal health and fetal development
  • Women pregnant with multiple gestations

Outcomes

Primary Outcomes

Change in Gestational Weight Gain

Time Frame: 0 weeks, 3 weeks, 5 weeks, 7 weeks, 9 weeks, 11 weeks, 13 weeks

Change in body weight from study baseline to 13 weeks

Change in Resting Energy Expenditure

Time Frame: 0 weeks, 3 weeks, 5 weeks, 7 weeks, 9 weeks, 11 weeks, 13 weeks

Change in resting energy expenditure, measued by indirect calorimetry, from study baseline to 13 weeks

Secondary Outcomes

  • Change in Total Sleep Time(0 weeks, 5 weeks, 11 weeks)
  • Change in Wake After Sleep Onset(0 weeks, 5 weeks, 11 weeks)
  • Change in Sleep Onset Latency(0 weeks, 5 weeks, 11 weeks)
  • Change in Mid-Sleep Point(0 weeks, 5 weeks, 11 weeks)

Study Sites (1)

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