University of Saskatchewan Research Initiative
Supporting better research through simple, consistent participation.
The RCT Research Platform helps eligible participants take part in a university-led randomized controlled trial. Participants can securely record daily study activities, follow their assigned plan, receive reminders, track progress, and stay connected with the research team.
Participation is voluntary. You may ask questions or withdraw according to the terms described in your consent materials.
- University-affiliated research
- Secure participant access
- Privacy-conscious data handling
- Direct research team support
About the Study
Research designed to learn from real-world participation.
This study is a randomized controlled trial affiliated with the University of Saskatchewan. The study uses structured participant groups and consistent daily reporting to help the research team examine its predefined research questions.
Participants may be assigned to a study group and, where applicable, an assigned product or study plan. The digital platform supports accurate daily reporting, timely reminders, participant communication, and responsible study administration.
The exact purpose, procedures, risks, potential benefits, eligibility requirements, and study duration will be explained in the official participant information and consent materials before enrollment.
This website provides a general overview. The approved consent form and information sheet are the authoritative sources for study participation.
At a glance
- Study type
- Randomized Controlled Trial
- Institution
- University of Saskatchewan
- Principal investigator
- Named in participant materials
- Department / unit
- University of Saskatchewan research unit
- Study location
- Saskatoon, Saskatchewan
- Expected duration
- Outlined in consent materials
- Ethics approval
- On file with the Research Ethics Board
Why consistent participation matters
Reliable research depends on clear procedures and consistent participant reporting. The RCT platform is designed to make everyday study activities easier to understand and record while helping the research team monitor study progress responsibly.
Structured research
Participant groups and predefined study procedures help the research team evaluate outcomes using a consistent research design.
Easier daily reporting
A straightforward mobile experience helps participants record required activities at the appropriate time.
Timely support
Reminders, notifications, and secure messaging help participants receive important study information and contact the research team.
Better study oversight
Participation trends and study activity records help authorized researchers identify follow-up needs without publishing personal participant information.
What participation may look like
Your exact activities will depend on the approved study protocol and the group to which you are assigned.
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Check eligibility
Review the initial eligibility information and contact the study team if you are interested.
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Learn about the study
A research team member explains the purpose, procedures, time commitment, possible risks, potential benefits, privacy practices, and your rights.
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Provide informed consent
You decide whether to participate after having the opportunity to ask questions. Participation is entirely voluntary.
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Receive participant access
If enrolled, you receive a unique participant ID and secure access instructions. Your participant ID should not be shared.
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Complete study activities
Follow your assigned study plan and record the requested daily information through the participant application.
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Stay connected
Receive reminders, monitor your progress, and securely contact the research team when you need assistance.
Assignment to a study group is determined by the approved research protocol. Participants may not be able to choose their group.
One simple place for your study activities
The participant application is designed to reduce uncertainty and make recurring study tasks easier to complete. Available features may vary depending on your study group and the current study phase.
Daily activity
See what needs to be recorded today.
Consumption logging
Record the time and quantity requested by the study protocol.
Progress and consistency
View recent participation, daily targets, and activity streaks.
Points and rewards
Where enabled by the study, earn points for eligible activities and view available rewards.
Notifications
Receive reminders and important updates from the study team.
Secure messaging
Ask questions and communicate directly with authorized research staff.
Points, rewards, and notifications are study-specific features. Availability, eligibility, limits, and fulfillment terms are determined by the approved study configuration.
Already enrolled? Use the participant ID and password provided by the research team.
Recognition for eligible study activities
Some study activities may qualify for points or rewards. The application can show your current points balance, eligible rewards, claim status, and applicable terms.
Earn
Complete eligible activities defined by the study.
Track
View your points history and progress.
Claim
Request eligible rewards and follow their fulfillment status.
Rewards are not guaranteed and may be subject to eligibility rules, availability, study limits, inventory, expiration dates, and verification by the research team. See the official reward terms for complete details.
Read reward termsWho may be eligible?
Eligibility is determined according to the approved study protocol. Completing an interest form does not guarantee enrollment.
A study team member will confirm eligibility before enrollment.
- Age requirementAdults 18+
- Location requirementSaskatchewan, Canada
- Health or dietary criteriaConfirmed during screening
- Smartphone / internetRequired for the app
- AvailabilityA few minutes daily
- Additional exclusionsReviewed during screening
Know what to expect
Before you consent, the research team will explain all required activities, appointments, possible costs, reimbursement arrangements, and circumstances that may affect your participation.
Privacy & Ethics
Your information deserves careful protection.
The RCT platform uses participant-based access to support study activities and authorized research administration. Study information is available only to authorized individuals according to their role and the approved research procedures.
Informed consent
You will receive approved study information and have the opportunity to ask questions before deciding whether to participate.
Voluntary participation
Taking part is your choice. Choosing not to participate will not affect your relationship with the University of Saskatchewan or your access to services.
Limited access
Authorized study personnel receive access appropriate to their responsibilities.
Responsible communication
Study notifications and messages are used to support participation and provide relevant study information.
Do not use the participant application for emergencies. If you need urgent medical assistance, contact local emergency services or an appropriate healthcare provider.
Meet the research team
This study is conducted by a multidisciplinary research team affiliated with the University of Saskatchewan.
Available to help with enrollment, study activities, and application access.
Real names, credentials, portraits, and affiliations are displayed only after institutional approval.
Designed around the participant experience
“Our goal is to make study instructions, daily reporting, and communication as clear and manageable as possible.”RCT Research Team
Frequently asked questions
What does RCT mean?
RCT stands for randomized controlled trial. It is a research design in which eligible participants are assigned to study groups according to a predefined protocol.
Is participation voluntary?
Yes. Participation is voluntary. You can ask questions before deciding whether to participate. Information about withdrawal and any applicable limitations will be explained in the consent materials.
Can I choose my study group?
Usually, group assignment is determined by the research protocol. The research team will explain the process before enrollment.
What will I need to record?
The required information depends on your assigned study plan. It may include the time and quantity of defined consumption activities and other approved study information.
How do I access the participant application?
Enrolled participants receive a unique participant ID and access instructions from the research team.
What if I forget my password?
Contact the study support team using the contact information on this page. Do not send sensitive personal or health information through an unsecured channel.
Can I edit an incorrect entry?
The application may allow recent entries to be corrected within a limited period. If an entry cannot be changed, contact the research team.
Will I receive reminders?
Where enabled, the application may send reminders and important study notifications. Notification availability may depend on your device settings.
Are points and rewards available?
Points and rewards may be available for specific eligible activities. The application will display the rules and terms that apply to your participation.
Is the participant chat for emergencies?
No. The participant chat is not an emergency or medical service. For urgent assistance, contact emergency services or an appropriate healthcare provider.
How is my information handled?
Information is handled according to the approved research protocol, consent materials, institutional requirements, and applicable privacy practices. Review the official privacy notice for complete details.
Who can I contact with questions?
Contact the study team at [email protected]. For questions about your rights as a research participant, contact the University of Saskatchewan Research Ethics Office.
Interested in taking part?
Learn more about the study, review the initial requirements, and contact the research team to find out whether participation may be right for you.
Already enrolled? Sign in to the participant application.
Submitting an expression of interest does not enroll you in the study and does not replace the informed consent process.
Contact the RCT research team
- Study email
- [email protected]
- Phone
- Provided upon enrollment
- Office hours
- Mon–Fri, 9:00–17:00 (CST)
- Study location
- Saskatoon, Saskatchewan
- Mailing address
- University of Saskatchewan, Saskatoon, SK, Canada
- Technical support
- [email protected]
- Participant rights
- U of S Research Ethics Office