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Optimized Recruitment to Drive Equitable Research in Stroke, Empowering Decision-making (ORDERed)

Study acronym: ORDERed
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Recruitment opened Start date changed from estimate of Apr 2026 to Aug 17, 2026 · Eligibility criteria expanded, about 14 words · Site details revised at 3 of 3 sites · 1 more Show 4 more changesShow less
    • Start date changed from estimate of Apr 2026 to Aug 17, 2026
    • Eligibility criteria expanded, about 14 words
    • Site details revised at 3 of 3 sites
    • Study description expanded, about 3 words
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
McMaster University
191 trials monitored
See 14 trials at risk
Stroke
3,289 trials monitored
See 141 trials at risk
Stroke is a major health issue, especially for women, who are more likely than men to have worse outcomes and lower quality of life after a stroke. Yet, women are under-represented in stroke research, which limits how well treatments work for them. This study aims to change that by testing a new way to recruit women into stroke research using the ORDER toolkit, a set of easy-to-understand, women-focused materials like brochures and videos co-designed with patients. This new approach will be compared to the usual way of recruiting patients. The study will track how many people join, how long it takes to make a decision, and what influences participation. Patients and research coordinators will also share their feedback on the process. Our goal is to make stroke studies more inclusive so that research findings benefit everyone equally.
Trial Details
NCT Number NCT07576647
Lead Sponsor McMaster University
Conditions Stroke, Stroke (CVA) or Transient Ischemic Attack
Enrollment 1,600 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov