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SMS Maama Project COVID-19

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Pregnancy Complications
Birth Injuries

Treatments

Behavioral: mHealth Platform

Study type

Interventional

Funder types

Other

Identifiers

NCT04739462
STUDY00010582

Details and patient eligibility

About

The study's purpose is to demonstrate the ability of an mHealth platform as a feasible way of sharing information in a time of restricted movement in order to inform future studies.

Full description

The primary objective of this trial is to assess whether an mHealth platform increases maternal health knowledge in the areas of birth preparedness, pregnancy, and birth complications as measured by the pre- and post-surveys in comparison to routine antenatal care.

The secondary objectives of this trial are;

  1. To provide knowledge of COVID-19 symptoms, transmission, diagnosis, and treatment, in a time of social distancing and learning.
  2. To improve access and linkages to maternal health services and information as well as provide appropriate referrals for pregnant females.
  3. Inform the adoption of mHealth into future health delivery plans.

Enrollment

248 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Own a personal mobile phone
  • Attend ANC at Kisenyi Health Centre IV, Kawempe Hospital or Rubaga Hospital
  • Are at least 24-26 weeks estimated gestational age
  • Literate in English or Luganda
  • Capable of sending/receiving text messages

Exclusion criteria

  • Females who plan to travel out of Uganda during the study period

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

248 participants in 2 patient groups

Intervention
Experimental group
Description:
Participants in this arm will receive the study intervention.
Treatment:
Behavioral: mHealth Platform
Routine Antenatal Care
No Intervention group
Description:
Participants in this arm will receive no intervention.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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