This project is part of an initiative that will provide evidence and strengthen capacity for bridging the knowledge gap in responding to the growing COVID-19 health crisis in the short-term and longer term.
This project is part of an initiative that will provide evidence and strengthen capacity for bridging the knowledge gap in responding to the growing COVID-19 health crisis both in the short-term and longer-term.
The Middle East and North Africa region is witnessing conflicts and protracted crises in many countries, including Syria, West Bank and Gaza, and Iraq, that result in massive population displacement to neighbouring countries.
There is a significant gap in data concerning the patterns and drivers of transactional sex, sexual exploitation, and abuse in transactional sex and their implications on the sexual and reproductive health and rights of refugees.
The aim of this scoping study is to conduct a thorough review and analysis of appropriate models for research hubs – often referred to as centres of research excellence – on adolescent sexual and reproductive health in the Middle East and North Africa (MENA) and in West Africa.
This project will support the Arab Council for Social Sciences (ACSS) to promote multidisciplinary research in health, livelihoods, and wellbeing in fragile and conflict contexts in the Middle East and North Africa.
This project will promote research evidence and data-informed decision-making and accelerate achievement of the Sustainable Development Goals (SDGs) in two selected countries in the Middle East namely Lebanon and Jordan.
The research will promote greater disaggregation of health information and inclusion of gender and social determinants of health indicators in Health Information Systems (HIS) at the national level in Egypt, Jordan and Morocco.
This project aims to generate knowledge on adolescents’ perceptions of and requirements for sexual and reproductive health (SRH) services among Palestinian refugee camp dwellers in the West Bank and Jordan.
The lack of reliable data limits the ability of health providers, planners, and community members to make informed decisions that can influence the well-being of women and children, particularly in vulnerable and undercounted populations.