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The National Aphasia Association invites researchers to share studies that seek to engage people with aphasia, their loved ones, and clinicians. We offer two ways to promote your work and connect with potential participants. If you are conducting an observational, qualitative, or other type of study that is not a clinical trial, see option 1 below. If you are conducting a clinical trial, follow option 2.

Option 1: Submit your study to the NAA via our online form

We welcome a wide range of study types, including but not limited to:

  • Observational studies, including neuroimaging studies and behavioral studies about language and other parts of cognition
  • Qualitative studies, including interviews and focus groups
  • Surveys
  • Technology and user experience studies

All studies submitted through our online form must be approved by the researcher’s Institutional Review Board (IRB). We’ll review your submission and—if appropriate—list it on our Join a Study page, making it easier for people with aphasia and their families to learn about and participate in your work.

Option 2: List your study on ClinicalTrials.gov

ClinicalTrials.gov is a publicly accessible database managed by the U.S. National Library of Medicine. It contains information about clinical research studies and their results.

You must register your study on ClinicalTrials.gov if it is:

  • An NIH-funded clinical trial, and/or
  • A clinical trial that meets federal regulatory requirements.

NAA’s Join a Study page has a “registered clinical trials” section, which will direct visitors to clinicaltrials.gov, where they can search and filter aphasia clinical trials as desired.

However, any clinical study involving human subjects—including observational and non-interventional studies—can be voluntarily registered. Studies must adhere to ethical and regulatory guidelines. This helps increase visibility and promote transparency.

How it works:

To register, you’ll use the Protocol Registration and Results System (PRS) to submit a study record. This includes:

  • Study title and description
  • Type of study and outcome measures
  • Interventions (as applicable)
  • Eligibility criteria
  • Other details

Information can often be pulled directly from the IRB application, consent forms, or study protocol. PRS staff will review your submission for accuracy before it is posted, and you will be required to make any changes if needed. You must verify or update your study record at least once per year. Results reporting may be required.

More information about posting a study to clinicaltrials.gov may be found here: https://clinicaltrials.gov/policy/faq

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