The Neuromodulation Service (NMS) provides comprehensive support for developing, refining, and optimizing neuromodulation protocols for research studies across campus. Whether you are designing your neuromodulation study, or adapting an existing protocol for a new population or experimental paradigm, our team is available to assist at every stage of development.
Study Design & Protocol Consultation
The NMS offers individualized consultation to help investigators create scientifically rigorous and feasible neuromodulation protocols. Support may include:
- Guidance on selecting stimulation modalities and parameters
- Recommendations on safety considerations and participant screening
- Integration of stimulation with behavioral, cognitive, or neuroimaging paradigms
- Development of sham, control, or blinding approaches
- Pilot testing and feasibility assessment
Our team works collaboratively to ensure protocols align with current best practices and are optimized for your specific research aims.
IRB Preparation & Regulatory Support
The NMS can assist investigators in preparing Institutional Review Board (IRB) submissions related to neuromodulation procedures. This includes:
- Drafting or refining protocol descriptions for IRB applications
- Providing standardized device language and safety documentation
- Guidance on reporting stimulation risks, safety monitoring, and adverse event procedures
- Support in addressing reviewer questions or revision requests
Our goal is to streamline the IRB process and help studies receive timely approval.
We welcome researchers at any stage of project planning—from early conceptualization to final protocol review. By partnering with the NMS, investigators gain access to technical expertise, equipment familiarity, and regulatory insight that strengthens study design and enhances participant safety.