Lifestyle Intervention Forever: Healthy Weight for Pregnancy and Birth (Pilot Study)

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Raul Artal, M.D., St. Louis University
ClinicalTrials.gov Identifier:
NCT01693666
First received: September 10, 2012
Last updated: March 4, 2014
Last verified: March 2014
  Purpose

Gaining too much weight in pregnancy is associated with adverse pregnancy complications and can have a long-term impact on maternal and offspring health, including increased risk for obesity and metabolic disease. Preventing excessive gestational weight gain could reduce adverse pregnancy outcomes and improve long-term health of mothers and offspring. Thirty obese (BMI ≥30) pregnant women will be recruited for this pilot study and randomly assigned to the Lifestyle Intervention ForEver (LIFE) program or routine care (RC). Participants will be enrolled before 18 weeks gestation and will be followed until 12 weeks after delivery. Women in the LIFE program will be given guidance on healthy eating and exercise at their regularly scheduled obstetric visits. To increase adherence to the program, a contingency management (CM) intervention offering incentives will be used to establish and maintain healthy nutrition and physical activity habits, working towards the goal of restricted weight gain (± 10lb) during their pregnancy. Three study testing visits will be scheduled for all participants: at study entry, 34-36 weeks gestation, and 12 weeks after delivering. Primary outcomes include adherence to the LIFE program, weight change in pregnancy and postpartum, and objective measures of maternal and offspring health.


Condition Intervention
Pregnancy
Obesity
Weight Gain
Obstetric Complications
Behavioral: Lifestyle intervention

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: Lifestyle Intervention Forever: Healthy Weight for Pregnancy and Birth (Pilot Study)

Resource links provided by NLM:


Further study details as provided by St. Louis University:

Primary Outcome Measures:
  • Gestational weight gain from study entry to delivery [ Time Frame: Approx. 20-25 weeks ] [ Designated as safety issue: No ]

    Maternal weight (lb) will be measured at program entry and at the time of delivery to determine weight gain during the study period.

    Pre-pregnancy body weight will be self-reported and used to estimate total gestational weight gain (lb).



Secondary Outcome Measures:
  • Change from baseline in maternal body composition [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]
    Changes in lean and fat mass will be examined at study entry, in late pregnancy (34-36 weeks gestation) and at 12 weeks postpartum

  • Change from baseline in maternal aerobic capacity [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]
    Peak aerobic capacity will be examined via a standard maximal oxygen consumption (VO2max) test performed on a stationary cycle ergometer at study entry, in late pregnancy (34-36 weeks gestation), and at 12 weeks postpartum

  • Maternal hormonal/metabolic changes from baseline [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]
    A fasted blood sample will be collected at study entry, in late pregnancy (34-36 weeks gestation) and at 12 weeks postpartum to examine changes in lipid profile and adipokines (TNF-alpha, leptin). Fasting glucose, insulin and C-peptide will also be measured and entered into the homeostatic model (HOMA) to estimate changes in insulin sensitivity and beta cell function during the study period.

  • Obstetric complications [ Time Frame: 1-25 weeks ] [ Designated as safety issue: Yes ]

    Parameters examined will include:

    • incidence rates of pregnancy complications (gestational diabetes mellitus, preeclampsia, gestational hypertension)
    • examination of obstetric parameters (mode of delivery, incidence of obstetric trauma, neonatal complications)

  • Change from baseline in maternal dietary intake [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]
    Dietary intake will be examined at study entry (15-18 weeks gestation), in late pregnancy (34-36 weeks gestation) and at 12 weeks postpartum.

  • Change from baseline in maternal psychometric outcomes [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]

    Psychometric outcomes examined at study entry, in late pregnancy (34-36 weeks gestation) and at 12 weeks postpartum include:

    • Quality of life
    • Depression and mood
    • Physical activity social support
    • Exercise self-efficacy

  • Offspring - fetal growth [ Time Frame: 10-25 weeks ] [ Designated as safety issue: Yes ]
    Fetal growth and abdominal circumference will be examined by fetal ultrasound at approximately 28-30, 34-36 and 38-40 weeks gestation and/or as part of routine care after 28 weeks gestation.

  • Neonatal size at birth [ Time Frame: Within 48 hours of birth ] [ Designated as safety issue: Yes ]
    Between group comparisons of birth size will include birth weight (g), crown-heel length (mm), head circumference (mm), body mass index (kg/m2), ponderal index. Population-specific standard deviation (SD) scores will be calculated and the incidence of small for gestational age, appropriate for gestational age and large for gestational age will be compared between groups.

  • Neonatal body composition at birth [ Time Frame: Within 48 hours of birth ] [ Designated as safety issue: No ]
    Neonatal lean and fat mass (g) will be calculated based on anthropometric measurements performed within 48 hours after birth

  • Offspring metabolic markers [ Time Frame: 20-25 weeks ] [ Designated as safety issue: No ]
    Concentrations of insulin-like growth factor (IGF)-I, IGF-II, IGF binding protein-1, IGF binding protein-3, glucose, insulin, leptin and triglyceride will be examined from cord blood samples taken at the time of delivery.

  • Pilot study outcomes [ Time Frame: 32-37 weeks ] [ Designated as safety issue: No ]

    The following pilot and feasibility outcomes will be assessed:

    • Participant recruitment rate (number of participants recruited per week)
    • Participant retention rate (percentage of participants completing all outcomes)
    • Adherence to the study program (completion of study data, food records, exercise sessions)
    • Success of the study program (percentage of participants achieving target gestational weight gain of plus/minus 10 lb)
    • Intervention dose (total intervention time in hours).

  • Postpartum weight retention at 12 weeks postpartum [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
    Maternal weight (lb) will be measured at 6 & 12 weeks postpartum and compared to delivery weight (lb) to determine postpartum weight retention.

  • Change from baseline in maternal physical activity levels [ Time Frame: 16-21 weeks ] [ Designated as safety issue: No ]
    Physical activity levels will be examined at study entry (15-18 weeks gestation), in late pregnancy (34-36 weeks gestation) and at 12 weeks postpartum.

  • Infant size at 12 weeks of age [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
    Between group comparisons of body weight (g), length (mm), head circumference (mm), body mass index (kg/m2), and ponderal index. Population-specific SD scores will be calculated and compared between groups.

  • Infant body composition at 12 weeks of age [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
    Infant lean and fat mass (g) will be calculated based on anthropometric measurements performed at 12 weeks of age.


Estimated Enrollment: 30
Study Start Date: September 2012
Estimated Study Completion Date: July 2014
Estimated Primary Completion Date: June 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lifestyle intervention group
The LIFE program emphasizes improved nutritional quality, moderate physical activity, and weight maintenance (±10 lb) in obese pregnant women using a contingency management (CM) approach to reinforce behavior change. Participants will meet with the study dietitian and exercise physiologist every 2-4 weeks to develop and maintain individualized nutrition and physical activity plans, reinforced by CM. When the subject meets with the interventionists at their regular appointments, they will review the diet and exercise requirements, and provide vouchers earned as reinforcement from the previous study period. Diet requirements include at least 5 days of food logs each week. Exercise requirements include objective verification of up to 5 exercise sessions per week (as prescribed).
Behavioral: Lifestyle intervention
No Intervention: Routine care group
Participants in the Routine Care (RC) control group will receive no additional intervention beyond standard of care.

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Women aged 18-40 years with a confirmed singleton pregnancy of up to 18 weeks gestation
  • Pre-pregnancy or early pregnancy BMI greater than or equal to 30 kg/m2

Exclusion Criteria:

  • Aged < 18 years or > 40 years
  • BMI < 30 kg/m2 at study screening
  • Multiple gestations
  • Previously diagnosed with type 1 or type 2 diabetes mellitus
  • Subjects will be excluded from the study if they present with any absolute or relative contraindications to exercise in pregnancy (as defined by ACOG); determined by completion of medical questionnaire by supervising physician
  • Any evidence of:

    i. Drug or alcohol abuse ii. Presence of any unstable psychiatric disorder iii. Plans to move away from the geographical area within the next nine months iv. Other medical or behavioral factors that, in the judgement of the supervising physician, may interfere with their ability to take part in a lifestyle intervention program during pregnancy.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01693666

Locations
United States, Missouri
Saint Louis University
Saint Louis, Missouri, United States, 63110
Sponsors and Collaborators
St. Louis University
Investigators
Principal Investigator: Raul Artal, MD St. Louis University
  More Information

No publications provided

Responsible Party: Raul Artal, M.D., Professor, St. Louis University
ClinicalTrials.gov Identifier: NCT01693666     History of Changes
Other Study ID Numbers: 22009, 8485, 22009
Study First Received: September 10, 2012
Last Updated: March 4, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by St. Louis University:
Pregnancy
Obesity
Weight gain
Obstetric complications
Lifestyle intervention

Additional relevant MeSH terms:
Obesity
Body Weight
Weight Gain
Overnutrition
Nutrition Disorders
Overweight
Signs and Symptoms
Body Weight Changes

ClinicalTrials.gov processed this record on September 22, 2014