Preventing Excessive Gestational Weight Gain Via Short Mobile Messages in WIC

Sponsor
University of Hawaii (Other)
Overall Status
Completed
CT.gov ID
NCT04330976
Collaborator
(none)
83
1
2
19.1
4.4

Study Details

Study Description

Brief Summary

The objective of this trial was to investigate the effect of educational short message service (SMS), or text messages, on gestational weight gain (GWG) in a low-income population.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Nutrition and physical activity intervention
  • Behavioral: Control
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
83 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Care Provider)
Primary Purpose:
Prevention
Official Title:
Preventing Excessive Gestational Weight Gain Via Short Mobile Messages in the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC)
Actual Study Start Date :
Oct 30, 2017
Actual Primary Completion Date :
Oct 29, 2018
Actual Study Completion Date :
Jun 2, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Nutrition and physical activity intervention

Behavioral: Nutrition and physical activity intervention
Messages sent on nutrition and physical activity in pregnancy

Other: Control

Behavioral: Control
Messages sent on general health during pregnancy

Outcome Measures

Primary Outcome Measures

  1. Change between pre-pregnancy weight and last weight taken before delivery [From date of randomization until delivery of child (e.g. up to 25 weeks)]

    Total weight gained during pregnancy

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 15-20 weeks gestational age and 18 years of age or older at time of recruitment

  • body mass index (BMI) of 25-45 kg/m2 in the first trimester

  • possession of a cellular phone with the ability to receive text messages without a charge

Exclusion Criteria:
  • conditions requiring a special diet

  • multiparous pregnancies

  • unable to consent to participate

  • unwilling to be randomized

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Hawaii Honolulu Hawaii United States 96822

Sponsors and Collaborators

  • University of Hawaii

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Hawaii
ClinicalTrials.gov Identifier:
NCT04330976
Other Study ID Numbers:
  • 5U54MD008149-09
First Posted:
Apr 2, 2020
Last Update Posted:
Apr 2, 2020
Last Verified:
Mar 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 2, 2020