Clinical research for category-defining evidence.
Custom protocol design, IRB approval, statistical analysis, and publication support. Built for sponsors who need full clinical-grade evidence.
What is Clinical Research?
Program OverviewClinical Research is our full-protocol research program for teams that need more than what a pilot can provide. Custom protocols, IRB approval, and clinical-grade methodology, designed to support regulatory claims, investor conversations, and peer-reviewed publication.
Why Clinical Research?
When you need clinical-grade evidenceCategory Leadership
Be the brand with published research that competitors can't replicate or dispute.
Regulatory Claims
IRB-approved protocols support structure/function claims with defensible evidence.
Publication-Grade Methodology
Methodology and data quality designed for peer-reviewed journal submission.
Investor Confidence
Clinical evidence that strengthens your position for fundraising and investor conversations.
Retail & Partnership Ready
Clinical evidence supports conversations with retailers and potential partners.
Long-Term Credibility
Peer-reviewed publications create lasting credibility and brand differentiation.
Program Features
What's IncludedCustom Protocol Design
Tailored study design with custom endpoints, inclusion/exclusion criteria, and methodology.
IRB Approval
Full Institutional Review Board approval for ethical oversight and regulatory compliance.
Statistical Analysis Plan
Pre-registered statistical methodology with formal analysis and p-value reporting.
Biomarker Collection
Option for blood draws, lab work, and biospecimen analysis when needed.
Publication Support
Manuscript preparation and journal submission guidance for peer-reviewed publication.
Large Cohort Studies
Scalable participant recruitment for statistically powered sample sizes.
What You'll Receive
DeliverablesClinical Study Report
A comprehensive research document suitable for regulatory submissions, investor presentations, and scientific communications.
- Executive summary with key findings
- Full methodology documentation
- Statistical analysis with significance testing
- Aggregate and segmented results
- Safety and adverse event reporting
Publication Manuscript
Journal-ready manuscript following CONSORT guidelines for peer-reviewed publication.
- CONSORT-compliant formatting
- Journal submission guidance
- Revision support through publication
Raw Data Package
Complete anonymized dataset for your own analysis and future research.
- Anonymized participant-level data
- Codebook and data dictionary
- Analysis scripts and methodology
Communications Package
Ready-to-use materials for sales, partnerships, and investor communications.
- Executive summary one-pager
- Key findings infographics
- Claim language guidance
The Research Process
Design to PublicationDiscovery & Protocol Design
We work with you to define objectives, endpoints, and methodology tailored to your specific claims and goals.
IRB Submission & Approval
Full ethical review and approval from an accredited Institutional Review Board, typically 4 to 6 weeks.
Recruitment & Data Collection
Qualified participant recruitment and rigorous data collection through our platform and wearable integrations.
Analysis & Reporting
Comprehensive statistical analysis, results interpretation, and clinical study report generation.
Publication & Activation
Manuscript submission support and guidance on activating your evidence across regulatory, partnership, and communication channels.
Ready to design a clinical study?
Let's discuss how a clinical study can help you build the evidence you need.