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The CCTR assists investigators and their teams to connect the community in participant engagement and recruitment for your study/research trial. The complimentary CCTR recruitment service includes:

  • Advertising your COUHES/IRB approved recruitment materials on our website.
  • Available to internal and external research colleagues.
  • Study advertisement posted on the newly created MIT centralized study recruitment repository.
  • Complimentary service (no charge).

Learn more about how to access the complementary study recruitment service.

Comparative Effectiveness of Migraine Preventive Medications: The APT Comparison Study

PI/Study Coordinator
Dr. Michael Lowney

Researchers across the United States are seeking volunteers with migraine, ages 18-70, to participate in a research study comparing the effectiveness of the medications atogepant (Qulipta) vs. propranolol (Inderal) vs. topiramate (Topamax).

You may be eligible to participate if:
1. You have migraine with or without Aura
2. You have at least 4 moderate to severe headaches a month
3. You have never taken these three medications before
4. You are willing to be randomly assigned to one of these medications

Participation will last for 16 weeks, with a possibility of up to 52 weeks, and includes 5-7 study visits (some in person in Hyde Park and some virtual). You will be asked to complete a headache diary and answer questionnaires.

You will receive $50 for each completed research visit, and $50 for each month during which you provide headache diary data on at least 80% of the days, up to a total of 4 months. If you complete the entire study, you will receive up to $550.

Contact name
Wonji Shin
Contact email
Info [at] ClinicalTrialsNE.com
Contact phone
617-827-1803