The first data challenge in a series, the** XPRIZE Mental Health Gender Data Challenge**, will incentivize teams to collect missing data that informs our understanding of how women experience depression and the factors that lead them to experience higher rates of depression and related concepts of distress.
The challenge is comprised of two rounds:
Round One: Proposal Submission
In Round One, teams will submit detailed proposals to a panel of expert judges appointed by XPRIZE in tandem with XPRIZE’s university partner. Once the competition is active, teams will have up to five months to submit their proposals. We expect proposals to contain the following minimum requirements:
- **Innovation Potential**: Proposed methods innovation or new forms of data collection or analysis.
- **Location**: Detail on the proposed research setting and evidence of the team’s understanding of the context and culture.
- **Methodology**: A description of the plan for collecting gender-disaggregated, qualitative and quantitative data on depression.
- **Partnerships**: A description of current and potential collaborative partnerships with government ministries, advocacy groups, research centers and universities, NGOs, and other organizations.
- **Qualifications**: Team member CVs and bios detailing qualifications and expertise relevant to the challenge.
- **Budget**: An overview of the proposed operational plan and budget.
- **Ethical Framework**: A locally adapted ethical framework that ensures the protection of human subjects, informed consent procedures, and data privacy and security protocols; and
- **Secure Data Accessibility**: Teams must consent to XPRIZE open access and accessibility requirements.
Round Two: Data Collection
During Round Two: Data Collection, teams will obtain Institutional Review Board (IRB) approval, complete research and data collection in the field (fieldwork), and ensure that data is prepared for submission. At the end of Round Two: Data Collection, judges will evaluate the quality and type of data collected by teams, and their effectiveness in carrying out the goals set forth in their Round One proposals.
Quantitative Data Requirements: Judges will evaluate teams’ quantitative data across a sections of criteria such as:
- **Interoperability**: Data files must be formatted in a manner that is easily accessible.
- **Secure Open Access**: Data collected by teams must be secure and protect user privacy.
- **Metadata**: Data collected must have the appropriate metadata and contextual information.
- **Contextual Coverage**: Data points collected must include a minimum set of demographic variables such as age, sex, gender, marital status, and employment status (with additional data points to be determined by our expert partnerships).
- **Statistically Significant Sample Size**: Data collection must be statistically significant for the research goals and population under scrutiny.
- **Clean**: Teams will be expected to detect and remove inaccurate or duplicative records to ensure that data collected is optimized for analysis.
- **Complete**: Judges will evaluate teams’ effectiveness in filling all required data fields.
- **Construct and Internal Validity**: For data collected, teams must evidence the relationship between data collected and depression diagnosis.
- **Disaggregation**: Data collected by teams must be sex and gender disaggregated.
Qualitative Data Requirements: Judges will evaluate qualitative data and the team’s report of their data collection process according to criteria such as:
- **Themes**: Does the data address a minimum of 90% of the specific themes of interest identified by XPRIZE?
- **Triangulation**: Has the team triangulated their findings with other sources (people, data, observations)? Have multiple methods been used to come to specific data points or conclusions? Are the methods consistent with the questions?
- **Saturation**: Was saturation achieved? Does the theme saturation have adequate justification based on the evidence available?<br>
- **Conformability**: Does the team leave an “audit trail” showing where their data came from and how it was collected? Are all procedures communicated?
- **Internal validity/Member checking**: Are the data trustworthy? Is there evidence that the data came from someone in that community and is a view that a person in that community would have?
- **Reflexivity**: Is there an articulation of how the researchers were reflexive and how they accounted for their presence and influence on the research process and data collection?
In your opinion, what is missing, or, what isn’t necessary?
We look forward to seeing all of your insights and feedback!