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Advancing Female University Students' Health Through Mobile Technology in Ethiopia

Advancing Female University Students Sexual and Reproductive Health, Nutrition, and Psychosocial Well-being Through Mobile Technology Interventions in Ethiopia

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07746791
Acronym
EMPOWER
Enrollment
880
Registered
2026-08-05
Start date
2026-08-01
Completion date
2028-06-30
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Intake, Psychosocial Wellbeing, Sexual and Reproductive Health

Keywords

Dietary intake, SRH, Ethiopia, Psychosocial wellbeing

Brief summary

Background: Female university students in Ethiopia experience a high burden of sexual and reproductive health, nutrition, and psychosocial problems, exacerbated by limited access to essential health services and support. Mobile technology provides an opportunity to deliver accessible, evidence-based health interventions. Objective: To evaluate the effectiveness of a mobile technology-based intervention in improving SRH, nutrition, and psychosocial well-being among female university students in Ethiopia. Methods: A concurrent mixed-methods study will be conducted among first-year female university students. Baseline quantitative and qualitative assessments will identify needs, barriers, and facilitators. A randomized controlled trial will evaluate a comprehensive mobile health education intervention delivered monthly. Quantitative data will be analysed using descriptive and inferential statistics, while qualitative data will undergo thematic analysis. Expected Outcomes: Improved sexual and reproductive health, dietary practices, and psychosocial well-being among female university students. Duration and Budget: The project will be implemented over the proposed study period with a total budget of 1,208,564 Ethiopian birr.

Detailed description

This is a mobile technology based interventional study to improve sexual and reproductive health, nutrition, and psychosocial wellbeing of female university students.

Interventions

BEHAVIORALBehavioural change intervention will be provided through mobile application

Behavioural change intervention will be provided through mobile application to improve sexual and reproductive health, nutrition, psychosocial, and appropriate digital use.The intervention packages or contents of the intervention will be developed based on the survey finding. Content of the intervention will include appropriate digital use, the basics of SRH, adolescent nutrition, psychosocial wellbeing, risk factors, and prevention measures. Nutrition messages will include nutrient requirements, the benefits of a healthy diet, the dietary habits of adolescents, the adverse consequences of junk food consumption, short- and long-term consequences of taking unhealthy diet. Possible solutions to improve dietary intake. A simple message about detailed description of the contents of the intervention will be delivered monthly through mobile technology for three consecutive years. Feedback will be collected from students after delivery of message to make sure whether students read or not.

BEHAVIORALRoutine care

Students in the control group will receive message provided through gender office.

Sponsors

Bahir Dar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Intervention model description

A two-arm parallel cluster randomized controlled trial will be conducted to assess the effect of mobile technology interventions on enhancing sexual and reproductive health, nutrition, and psychosocial Well-being among Female University Students in Ethiopia.

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Regular undergraduate female university student will be included in the study. * First year female students will be included in the study.

Exclusion criteria

• Students who have no mobile phone will be excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Dietary intakeBaseline assessment will be done from August 1-September 30, 2026 (8 weeks) and endline assessment will be done from April to May 2028 (8 weeks).Dietary intake will be the primary outcome and will be measured using food frequency questionnaire. Students who have a higher score for healthy foods will be considered as having appropriate dietary practice, otherwise not.
Sexual and reproductive healthBaseline assessment will be done from August 1-September 30, 2026 (8 weeks) and endline assessment will be done from April to May2028 (8 weeks) .Sexual and reproductive health will be the primary outcomes and will be assessed using questionnaires.
Psychosocial well-beingBaseline assessment will be done from August 1-September 30, 2026 (8 weeks) and endline assessment will be done from April to May2028(8 weeks) .Psychosocial well-being will be the primary outcomes of this studyand will be assessed using questionnaires.

Countries

Ethiopia

Contacts

CONTACTYeshalem M Demilew, PhD
yeshalem_mulugeta@yahoo.com+251954342535
CONTACTElenie A Mengesha, PhD
+251918772775

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026