W21C reviews all new services requests to ensure that the project fits within the mandate of the W21C and is aligned with the team’s research expertise and capacity. Please contact us to set up a meeting to review your project’s needs, based on this we will work with you to develop a plan and identify resources to get you moving in the right direction.
Support for protocol development, independent third-party review, or connection with subject matter experts and investigators.
Coordination support includes the start-up, initiation, and ongoing management of the trial.
Clinical simulations can evaluate new clinical pathways, identify process improvement and optimization, and enhance hands-on learning experiences. W21C’s Healthcare Human Factors Simulation Laboratory, a highly adaptable observational environment, can be configured to create realistic scenarios and spaces that are comparable to actual healthcare environments.
Involves the equal partnership of individuals who experience the healthcare system, specifically patients and their families, and healthcare staff. We work with these groups to identify their needs and potential solutions, making full use of each other’s knowledge, resources, and contributions to achieve better outcomes or improved efficiency.
Ongoing entry, privacy, security, and validation of data collected throughout the study, in addition to maintenance of case report forms, and adverse events to trial sponsors.
Drafting and submission of the required ethics applications to the University of Calgary’s Conjoint Health Research Ethics Board. Includes maintenance of ethics applications, such as amendments and reporting.
Assessment of the safety and efficacy of physical spaces such as facility layouts, workstation configurations, and hospital rooms. In addition to understanding the processes and variables of the health care system as whole. Both these evaluation methods can be paired with an interactive design of the environment.
A detailed expert examination of product designs against a set of standardized usability guidelines to identify design issues that may negatively impact the user experience during product interaction. This is a cost-effective evaluation that provides rapid, but detailed feedback on the evaluated system (e.g., digital interfaces, physical products).
Compiling and entering necessary information for funding competitions such as the Canadian Common CV, ResearchNet applications, budgets, methods, and Knowledge Translation plans.
An iterative design approach that focuses on the needs of the users by engaging them in every phase of the design process. This approach allows you to understand your user, what they want and don’t want from your design, and how they’re ultimately going to interact with each part of your product.
Embedded within each of our projects, Knowledge Translation (KT) is a dynamic and iterative research process to create and translate new knowledge to improve health and healthcare. Support can be provided for KT planning, knowledge synthesis (interpreting and integrating existing evidence before designing and conducting additional research), exchange (informing evidenced-based decision-making) and dissemination through paper writing, conference presentations, and media engagement.
Examination and summary of current published information and the state of a topic to inform future research in the area. Support can be provided with identification of the type of literature search required, establishing the relevant databases, search strategy design, data synthesis and interpretation, and writing.
Provision of medical expertise for clinical integrity, validity, and safety for the design and duration of the trial.
A process to determine the healthcare needs for a product, service, workflow or system innovation. It is used to establish the feasibility and utility of the proposed concept and identify areas for further consideration before additional investments are made. Results can be used as a strategic starting point for innovations in healthcare.
Support includes the identification and randomization of eligible study participants, development of study recruitment materials, obtaining participant consent, and the administration of an intervention.
Drafting, submission, and maintenance of required documents to register the clinical trial of a medical device, drug, or process with regulatory agencies.
Collection of biological materials and transport to a laboratory for third-party analysis (including phlebotomy and venipuncture services).
Based on the research needs, we can identify and apply the appropriate tools to generate the best data from your stakeholders and participants. We can design and facilitate structured workshops, focus groups, or interviews to gather viewpoints or opinions from relevant user groups.
Assisting with design, development, distribution, data compilation, and analysis of surveys and questionnaires that can be used to gather demographics, attitudes, or previous experiences. This information can be used to target new products, inform further design, or evaluate the effectiveness of an intervention or program.
A method to evaluate a product or service by putting it into the hands of the end-users. Usability testing can be applied at any stage of development. Identifying and addressing usability problems early in the development process is more cost-effective, and results in more usable and satisfying products.
The user experience (UX) of digital interface focusses on understanding all aspects that contribute to the end user’s interaction with the system. The inclusion of UX design throughout the entire development process will help you understand and map user needs, product goals, and provide recommendations to mitigate potential usability issues. Digital interfaces can include websites, online platforms, and mobile applications.
- "W21C helped me make the most of seed grant funding. They took on the project management, hiring staff and managing budget administration so that I could rapidly get moving on the core work of my clinical research project. W21C is such a valuable set up for new researchers and clinician-researchers wondering how to turn an idea into meaningful results. The can-do attitude and network of bright minds that you meet there inspires you to innovate!"
- “W21C was a critical partner for Surface Medical Inc. in the development and launch of our flagship product, CleanPatch®. They performed a comprehensive clinical needs assessment that helped confirm product requirements, further validated market opportunity, and demonstrated market need. W21C also organized focus group sessions with key stakeholders that generated important feedback and influenced the final product design. In addition, W21C helped secure funding to execute the clinical needs assessment with a leading Canadian hospital, which demonstrated the clinical performance and usability of CleanPatch®. CleanPatch® has been adopted today globally and has become the standard of care in multiple leading healthcare institutions. We would strongly recommend working with W21C to evaluate novel healthcare ideas.”
- "The W21C helped our program identify new process improvement ideas, which in turn allowed us to implement solutions that increased our overall efficiency and quality of care we provide to our patients. The W21C was able to expand upon on our current patient care model by allowing us to step back and find previously unidentified patterns and connections that turned into new ideas and solutions. The support the W21C provide our Community Paramedic program was fantastic and we continue to implement solutions based on the recommendations created by the W21C team."
- "Working with W21C has been helpful to our product development process. Having access to the hospital and healthcare professionals has provided use case scenarios and relevant feedback. When dealing with novel technology W21C has been receptive to new ideas and how they can make positive impacts in healthcare."