Iron Deficiency Anemia Clinical Trials

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FACE-APPS-Based Approach for Improving Iron Deficiency Anaemia Indicators Among Female Adolescents at Marginalized Communities: A Randomized Control Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to evaluate the effect of the Face-to-face Assisted Counselling with Enhanced Application School-Based Approach (FACE-APPS-Based Approach) on anemia indicators among female adolescents. The study is a prospective, randomized controlled trial. A total of 160 female adolescents with hemoglobin levels below 12.0 g/dL will be recruited from 7 secondary schools. Random assignment at the individual level, stratified by baseline anemia status, will be used to ensure balance. For participants in the intervention group, the intervention will be designed by an interdisciplinary team and administered over 4 months, comprising 8 face-to-face counseling sessions and 8 parallel mobile application modules. Control group participants will receive standard care (diagnosis and referral). The primary outcomes are the mean differences in hemoglobin and serum ferritin levels. Secondary outcomes are engagement among female adolescents (attendance at counseling sessions and completion of mobile application modules).

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 14
Maximum Age: 14
Healthy Volunteers: t
View:

• Adolescent females aged 14-17 years

• who are attending high school

• who have haemoglobin levels \<12 mg/dl and serum ferritin levels below 15 μg/L

Locations
Other Locations
Saudi Arabia
Administration of Education, Secondary Schools
RECRUITING
Wadi Addawasir
Contact Information
Primary
Mahmoud Ahmed Elsheikh, PhD
mr.mash87@cu.edu.eg
00201066309578
Time Frame
Start Date: 2026-05-24
Estimated Completion Date: 2026-11-30
Participants
Target number of participants: 160
Treatments
Experimental: Intervention group: FACE-APPS-Based approach
The intervention will be delivered over 8 counselling sessions with the adolescents at schools and 8 modules of a mobile application. Each counselling session lasts 60-90 minutes. The sessions will be conducted by a researcher and a trained nurse. The 8 modules of a mobile application were designed as a self-learning package. Each module takes 20 minutes of study followed by 10 minutes of 10 MCQs. A counselling session and a mobile application module will be experienced biweekly for 4 months. Additional support: reminders via app notifications, and peer group discussion via the application.~The educational content was structured to systematically address the core constructs of Pender's Health Promotion Model (HPM).
No_intervention: Control group: Standard care
Adolescents in the IG will receive standard care. They will receive routine medical insurance care.
Related Therapeutic Areas
Sponsors
Collaborators: Prince Sattam Bin Abdulaziz University, Northern Border University, Ain Shams University
Leads: Cairo University

This content was sourced from clinicaltrials.gov