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Interactive Mobile Health Intervention to Improve Early Postpartum Modern Contraceptive Method Uptake

Not Applicable
Completed
Conditions
Other Cardiovascular Diseases of Mother, Postpartum
Interventions
Behavioral: Mobile health intervention(mHealth)
Registration Number
NCT05666037
Lead Sponsor
Wollo University
Brief Summary

The main aim of this study is to determine effectiveness of mobile health intervention to improve early postpartum modern contraceptive service uptake among postpartum women in Dessie and Kombolcha town zones, North east Ethiopia. This study will be conducted in Dessie and Kombolcha zones in Amhara region, North east Ethiopia. The largest sample size will be taken and total sample size will be 784.

Detailed Description

The main aim of this study is to determine effectiveness of mobile health intervention to improve early postpartum modern contraceptive service uptake among postpartum women in Dessie and Kombolcha town zones, North east Ethiopia. This study will be conducted in Dessie and Kombolcha zones in Amhara region, North east Ethiopia. The largest sample size will be taken and total sample size will be 784.

Cluster randomized control trial behavioral intervention sampling technique will be deployed. First participants will be grouped in to two arms based on randomization of clusters. The intervention arm will take the new mobile health intervention with existed health care practice and the control arm will take the existed current health care practice. Intervention mobile health messages will be developed from family planning behavior change framework and national guidelines. Data will be collected by using pre-tested interviewer administered structured questionnaires. Data will be collected in four different phases. Open data kit (ODK) will be used for data collection. Duration of intervention will be 4 months. Descriptive analyses will be made by computing proportions and summary statistics. Statistical package to social science (SPSS.26) and STATA.15 soft wares will be used to do analysis. Structural Equation Modeling (SEM) or path analysis will be done to identify the fitted components to determine latent variables.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
784
Inclusion Criteria

All mothers who will be 24-28 week of gestation and have access to mobile phone in the study area will be recruited to this study.

Exclusion Criteria
  • Pregnant women, who will be assumed to have serious medical problems, will be excluded.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupMobile health intervention(mHealth)The intervention group will receive mobile health intervention.
Primary Outcome Measures
NameTimeMethod
Early postpartum family planning is outlined as women who have will be used any kind of modern birth control technique at intervals the primary six weeks when she gave birth.Two weeks after intervention completed the outcome will be measured.

If the respondent answers yes it will be coded "1" and if not coded as "0"

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dessie and Kombolcha

🇪🇹

Dessie, South Wollo, Ethiopia

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