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Clinical Trials

Drafting Clinical Trial Registrations

Our approach to drafting clinical trial registrations involves a research technician, graduate student, and/or postdoctoral researcher taking the initial step in preparing the registration. When drafting the clinical trial registration, make sure you have access to the relevant grant and IRB application that pertains to the trial.

You may use this template as a guide for your draft. However, it's essential to check the registration site for any updates, such as new sections being added or existing ones being removed. If you notice any changes, promptly update the template with track changes to reflect them.

If you come across valuable insights regarding what should be included in a specific section or find any helpful resources, please incorporate them into the template so that other team members can benefit.

Once your draft is complete, Aaron and Susanne will review it and provide the necessary approvals for posting the registration on clinicaltrials.gov. Please remember that clinical trials must be registered within 21 days of enrolling the first participant. You will need a PRS account to be created for you before you can register the trial. See these sections for instructions on how to obtain a PRS account.

Registered Clinical Trials

We have a number of clinical registrations that are currently in data collection or completed. Below are the links to the registrations:

Auditory Training

Executive Functioning Training

Vision Training

Visual Arts-Based Interventions

Obtaining Clinicaltrial.gov PRS Account at Northeastern

ClinicalTrials.gov Protocol Registration and Results System (PRS) accounts are necessary for registering clinical trials. To request an account, please contact Madison Leary with a cc to Curtis Van Slyck.

Research Performance Progress Reports (RPPRs)