Sign in

NCT04449432Completed

Goals for Reaching Optimal Wellness: GROWell

Source: ClinicalTrials.gov · Last updated 7 Aug 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
480 (actual)
First submitted
23 Jun 2020
Start date
14 Dec 2020
Primary completion date
26 Jan 2024
Lead sponsor
University of California, Davis
Diseases
Obesity
NCT number
NCT04449432

What you commit to

  • Study type: Interventional
  • Participants enrolled: 480
  • From 14 Dec 2020 to the primary completion date, 26 Jan 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Quit smoking \<6 months prior to enrollment

Other

  • Known pregnancy or fetal complications/high-risk status
  • Multiple gestation
  • Unable to read/write English
  • BMI \>40
  • Current smokers

Who the study is looking for

  • 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

Age in the registry: 18 years to 44 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UC DAVIS
Coordinator of this site? Confirm its status
DavisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.