Category leadership.
Build human research behind your product, with an optional pathway toward peer-reviewed publication.
Clinical research
Clinical research for category-defining evidence.
Custom protocol design, IRB approval, and statistical analysis. Publication and journal-submission support are available as optional add-ons.
Schedule a Call
Custom protocolsIndependent ethical reviewEvidence your team can use
Program overview
What is a full clinical study?
A full clinical study is our complete-protocol research program for teams that need more than a pilot provides.
Custom protocols, IRB approval, and clinical-grade methodology, designed to support regulatory claims and investor conversations. If publication support is separately scoped, the study can also be prepared for journal submission.
Protocols typically run 1 to 6 months, with multi-arm and parallel designs supported.
When you need clinical-grade evidence
Why a full clinical study?
Evidence behind your claims.
Design the study around the claim you want to evaluate, with conclusions matched to the evidence produced.
Publication-ready rigor.
Methodology and data quality that can support a journal submission when publication services are separately scoped.
Investor confidence.
Clinical evidence that strengthens your position for fundraising and investor conversations.
Stronger partnerships.
Clinical evidence that supports conversations with retailers and potential partners.
Lasting credibility.
If a submitted manuscript is accepted and published, peer-reviewed research can create lasting credibility and brand differentiation.
Program scope
Core and optional services.
Core services
Tailored study design
Custom endpoints, inclusion/exclusion criteria, and methodology, including multi-arm and parallel designs.
IRB approval
Full Institutional Review Board approval for ethical oversight.
Statistical methodology
Pre-registered statistical methodology with formal analysis and p-value reporting.
Optional services
Lab work, when needed
Option for blood draws, lab work, and biospecimen analysis when needed.
Optional publication support
A separately scoped add-on for manuscript preparation and journal submission guidance. Acceptance and publication are not guaranteed.
Scalable recruitment
Scalable participant recruitment for statistically powered sample sizes.
Deliverables
Available deliverables.
Built for use, not for the file drawer. Your agreed study scope defines which deliverables are included.
Optional publication services
Manuscript preparation, journal submission guidance, and revision support are separately scoped services. They are not included automatically, and journal acceptance or publication is never guaranteed.
The research
Clinical 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
The translation
Communications package.
The results, translated for every stakeholder who has to act on them: marketing review, partners, investors, and counsel.
- Executive summary one-pager
- Key findings infographics
- Claim language guidance
Claim language follows the study design and findings.
The data
Anonymized dataset.
An anonymized dataset for your own analysis and future research, subject to the protocol, consent, and agreed data-access scope.
- Anonymized participant-level data
- Codebook and data dictionary
- Analysis scripts and methodology
Optional add-on
Scientific manuscript.
When separately scoped, a manuscript can be prepared following the appropriate reporting guideline, including CONSORT for randomized designs.
- Design-appropriate reporting and formatting
- Journal submission guidance
- Revision support for journal responses, if separately scoped
Not included automatically. Journal acceptance and publication are determined independently and are not guaranteed.
Study workflow
The research process.
Discovery and protocol design.
We work with you to define objectives, endpoints, and methodology tailored to your specific claims and goals.
IRB submission and approval.
Full ethical review and approval from an independent Institutional Review Board. Timing depends on the protocol and review requirements.
Recruitment and data collection.
Qualified participant recruitment and rigorous data collection through our platform and wearable integrations.
Analysis and reporting.
Comprehensive statistical analysis, results interpretation, and clinical study report generation.
Optional publication and activation.
When separately scoped, we can support manuscript submission and help activate your evidence across regulatory, partnership, and communication channels. Journal acceptance and publication are not guaranteed.
Another way in
Want an earlier read first?
A pilot study tests for signal on a smaller scope. Some teams run one first, some run both, and some come straight here.
Ready to design a clinical study?
Let's discuss how a full study can help you build the evidence you need.