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Clinical Trials/NCT05666037
NCT05666037
Completed
N/A

Effectiveness of Interactive Mobile Health Intervention to Improve Early Postpartum Modern Contraceptive Method Uptake Among Women in North East Ethiopia: Community Based Cluster Randomized Control Trial

Wollo University1 site in 1 country784 target enrollmentDecember 5, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Other Cardiovascular Diseases of Mother, Postpartum
Sponsor
Wollo University
Enrollment
784
Locations
1
Primary Endpoint
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.
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
December 5, 2022
End Date
June 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Wollo University
Responsible Party
Principal Investigator
Principal Investigator

Niguss Cherie

Assistant professor

Wollo University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

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.

Time Frame: 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"

Study Sites (1)

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