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Goals for Reaching Optimal Wellness: GROWell

Primary Purpose

Pregnancy Related, Gestational Weight Gain, Postpartum Weight Retention

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
GROWell (Interactive Obesity Treatment Approach)
Attention Support Control
Sponsored by
University of California, Davis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pregnancy Related focused on measuring pregnancy, gestational weight gain, postpartum weight retention, overweight, obesity, diet, mHealth, digital health

Eligibility Criteria

18 Years - 44 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • 10-16 weeks gestation of a confirmed pregnancy (i.e., ultrasound/heartbeat detected)
  • Nulliparous or >12 months since previous birth
  • Receive care at one of eight UC Davis Obstetric Clinics and plan to deliver at UC Davis Medical Center
  • BMI >25 and <40 who are willing to receive and respond to texts using their own cell phone or a study-provided phone

Exclusion Criteria:

  • Known pregnancy or fetal complications/high-risk status
  • Multiple gestation
  • Unable to read/write English
  • BMI >40
  • Current smokers
  • Quit smoking <6 months prior to enrollment

Sites / Locations

  • UC DavisRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

GROWell (Interactive Obesity Treatment Approach)

Attention Support Control

Arm Description

With Self-regulation Theory as the framework, the Interactive Obesity Treatment Approach Adapted for Pregnancy/Postpartum includes four components: (1) personalized goal setting, (2) daily support and educational messages, (3) self-monitoring of behavior with tailored feedback, and (4) skills training. Each component aligns with the self- regulatory processes shown in previous studies to be necessary for behavior change. All interactions with participants are via text using a cell phone.

The attention control will be delivered using text messaging to reduce the potential placebo effect that interacting with our mHealth system may have on pregnancy weight gain and postpartum weight loss. Information will be provided to control group participants that is specific to pregnancy, labor, delivery, and early infancy, but not to diet. Texts are specific to the participant's partner, pregnancy, employment, and breastfeeding plans/status.

Outcomes

Primary Outcome Measures

Gestational Weight Gain
Gestational weight gain will be calculated as: [weight(delivery) - weight(preconception)]. Women will be categorized as gaining excess gestational weight if they started pregnancy as overweight and gained more than 25 pounds or started pregnancy as obese and gained more than 20 pounds.
Postpartum Weight Retention
Postpartum weight retention will be calculated as: [weight(6 months postpartum) - weight(preconception)]. Women will be categorized as experiencing postpartum weight retention if postpartum weight at 6 months is greater than 1.05*preconception weight.

Secondary Outcome Measures

Adherence to text-based self- monitoring
Measured cumulatively by week as the number of times a participant responds to weekly prompts to report on her progress to the number of times she was prompted, calculated to a percent separately for prenatal and postnatal periods.
Adherence to prescribed goals
Measured cumulatively by week as the proportion of goals for which a participant has "good adherence" during the previous week, defined as adhering to the goal 5/7 days, or >70%, calculated to a percent and separately for prenatal and postpartum periods.

Full Information

First Posted
June 23, 2020
Last Updated
April 26, 2022
Sponsor
University of California, Davis
Collaborators
Duke University, Pattern Health, National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT04449432
Brief Title
Goals for Reaching Optimal Wellness: GROWell
Official Title
Goals for Reaching Optimal Wellness: GROWell
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 14, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis
Collaborators
Duke University, Pattern Health, National Institute of Nursing Research (NINR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite the negative consequences to maternal-child health from women gaining too much weight during pregnancy, up to 62% of overweight and obese women gain more pregnancy weight than is recommended. This project will establish the efficacy of Goals for Reaching Optimal Wellness (GROWell), an mHealth tool for achieving appropriate pregnancy weight gain and promoting postpartum weight loss among women who enter pregnancy overweight or obese. GROWell will fill a gap in research and clinical care by providing a validated, standalone mHealth tool for weight control during pregnancy and postpartum, which is a currently lacking resource.
Detailed Description
Research attempts to prevent excess gestational weight gain, defined as gaining more weight during pregnancy than Institute of Medicine (IOM) guidelines for prepregnancy body mass index (BMI), have largely been unsuccessful. Roughly 62% of overweight and 45% of obese women still gain more weight than recommended, increasing risk for postpartum weight retention. Few mobile health (mHealth) interventions have been trialed to address pregnancy-associated weight gain, which is a missed opportunity. Adult women are high users of technology for general and pregnancy-specific health information seeking and sharing. To fill this gap, the long-term goal of this research is to disseminate into clinical practice a standalone mHealth tool that is effective for overweight and obese pregnant women to achieve gestational weight gain within IOM recommendations and return to prepregnancy weight after childbirth. The goal of this application is to test GROWell: Goals for Reaching Optimal Wellness, an innovative, mHealth tool based on Self-regulation Theory that investigators designed in pilot work to achieve appropriate gestational weight gain and safe postpartum weight loss. The investigators propose a blinded, randomized controlled trial to test the efficacy of GROWell compared to an attention control also developed in a pilot. Investigators will recruit 480 women ages 18-44 with prepregnancy BMI 25-<40 and 10-16 weeks gestation of a singleton, uncomplicated pregnancy. Block randomization based on BMI, race, and recruitment clinic will be used to assign participants equally to arm 1, GROWell (n=240), or arm 2, the attention control (n=240). Upon study enrollment and through 6 months postpartum, GROWell participants will receive daily text messages that provide tailored education, problem-solving skills, and support to aid their personalized dietary goals. Once weekly, participants self-monitor overall adherence to their goals using text messages that prompt them to report on how they did in the past week. When users respond to this prompt, they immediately receive a text with tailored feedback on their adherence and long-term progress toward their goals. Control participants will receive weekly texts that provide personalized self-care, pregnancy, labor, delivery, and early infancy education. The specific aims are to: (1) Compare the efficacy of GROWell to the attention control in reducing the proportion of women who gain excess gestational weight based on IOM guidelines (>25 lbs for overweight and >20 lbs for obese) controlling for demographics, parity, physical activity, diet quality, and depression/anxiety; and (2) Compare the efficacy of GROWell to the attention control in reducing postpartum weight retention at 6 months post-birth as measured by the proportion of women who are within 5% of their prepregnancy weight, controlling for demographics, parity, physical activity, diet quality, breastfeeding, and depression/anxiety. This research addresses PA 18-135 (Maternal Nutrition and Pre-pregnancy Obesity) and will provide an innovative, evidence-based, standalone mHealth tool to reduce excess gestational weight gain and postpartum weight retention among overweight and obese women, currently an unavailable resource.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy Related, Gestational Weight Gain, Postpartum Weight Retention, Overweight and Obesity
Keywords
pregnancy, gestational weight gain, postpartum weight retention, overweight, obesity, diet, mHealth, digital health

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Comparing intervention to active control
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
480 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GROWell (Interactive Obesity Treatment Approach)
Arm Type
Experimental
Arm Description
With Self-regulation Theory as the framework, the Interactive Obesity Treatment Approach Adapted for Pregnancy/Postpartum includes four components: (1) personalized goal setting, (2) daily support and educational messages, (3) self-monitoring of behavior with tailored feedback, and (4) skills training. Each component aligns with the self- regulatory processes shown in previous studies to be necessary for behavior change. All interactions with participants are via text using a cell phone.
Arm Title
Attention Support Control
Arm Type
Active Comparator
Arm Description
The attention control will be delivered using text messaging to reduce the potential placebo effect that interacting with our mHealth system may have on pregnancy weight gain and postpartum weight loss. Information will be provided to control group participants that is specific to pregnancy, labor, delivery, and early infancy, but not to diet. Texts are specific to the participant's partner, pregnancy, employment, and breastfeeding plans/status.
Intervention Type
Behavioral
Intervention Name(s)
GROWell (Interactive Obesity Treatment Approach)
Intervention Description
Personalized messaging via cell phone to support healthy eating behaviors during pregnancy and through 6 months postpartum
Intervention Type
Behavioral
Intervention Name(s)
Attention Support Control
Intervention Description
Personalized messaging via cell phone to support healthy behaviors during pregnancy and through 6 months postpartum
Primary Outcome Measure Information:
Title
Gestational Weight Gain
Description
Gestational weight gain will be calculated as: [weight(delivery) - weight(preconception)]. Women will be categorized as gaining excess gestational weight if they started pregnancy as overweight and gained more than 25 pounds or started pregnancy as obese and gained more than 20 pounds.
Time Frame
Mid-study (25-30 weeks)
Title
Postpartum Weight Retention
Description
Postpartum weight retention will be calculated as: [weight(6 months postpartum) - weight(preconception)]. Women will be categorized as experiencing postpartum weight retention if postpartum weight at 6 months is greater than 1.05*preconception weight.
Time Frame
End of study (50-55 weeks)
Secondary Outcome Measure Information:
Title
Adherence to text-based self- monitoring
Description
Measured cumulatively by week as the number of times a participant responds to weekly prompts to report on her progress to the number of times she was prompted, calculated to a percent separately for prenatal and postnatal periods.
Time Frame
mid-study (25-30 weeks) and post-study (50-55 weeks)
Title
Adherence to prescribed goals
Description
Measured cumulatively by week as the proportion of goals for which a participant has "good adherence" during the previous week, defined as adhering to the goal 5/7 days, or >70%, calculated to a percent and separately for prenatal and postpartum periods.
Time Frame
mid-study (25-30 weeks) and post-study (50-55 weeks)
Other Pre-specified Outcome Measures:
Title
Delivery type
Description
Categorical as cesarean or vaginal delivery
Time Frame
mid-study (25-30 weeks)
Title
Fetal growth abnormalities
Description
categorical as small-for-gestational age, large-for- gestational-age, macrosomia, or none.
Time Frame
mid-study (25-30 weeks)
Title
Pregnancy complications
Description
categorical as gestational diabetes, hypertension, preeclampsia/eclampsia, placental abruption, fetal death, antepartum admission, preterm birth with and without NICU admission, none
Time Frame
mid-study (25-30 weeks)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 10-16 weeks gestation of a confirmed pregnancy (i.e., ultrasound/heartbeat detected) Nulliparous or >12 months since previous birth Receive care at one of eight UC Davis Obstetric Clinics and plan to deliver at UC Davis Medical Center BMI >25 and <40 who are willing to receive and respond to texts using their own cell phone or a study-provided phone Exclusion Criteria: Known pregnancy or fetal complications/high-risk status Multiple gestation Unable to read/write English BMI >40 Current smokers Quit smoking <6 months prior to enrollment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
William Pacuilla
Phone
(530) 754-8280
Email
bpacuilla@ucdavis.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Grace Liu
Phone
(530) 754-8323
Email
proposals@ucdavis.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leigh Ann Simmons, PhD
Organizational Affiliation
University of California, Davis
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Davis
City
Davis
State/Province
California
ZIP/Postal Code
95616
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Grace Liu, JD
Phone
530-754-7700
Email
proposals@ucdavis.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36185388
Citation
Simmons LA, Phipps JE, Whipps M, Smith P, Carbajal KA, Overstreet C, McLaughlin J, De Lombaert K, Noonan D. From hybrid to fully remote clinical trial amidst the COVID-19 pandemic: Strategies to promote recruitment, retention, and engagement in a randomized mHealth trial. Digit Health. 2022 Sep 25;8:20552076221129065. doi: 10.1177/20552076221129065. eCollection 2022 Jan-Dec.
Results Reference
derived
PubMed Identifier
34813963
Citation
Simmons LA, Phipps JE, Overstreet C, Smith PM, Bechard E, Liu S, Walker C, Noonan D. Goals for Reaching Optimal Wellness (GROWell): A clinical trial protocol of a digital dietary intervention for pregnant and postpartum people with prenatal overweight or obesity. Contemp Clin Trials. 2022 Feb;113:106627. doi: 10.1016/j.cct.2021.106627. Epub 2021 Nov 20.
Results Reference
derived
Links:
URL
https://studypages.com/s/healthy-pregnancy-study-720304/
Description
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