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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorMcMaster University

About this trial

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.

Eligibility criteria

Qualifiers

All patients, regardless of age or baseline disability, seen in urgent TIA/stroke clinics and referred from the emergency department for suspected TIA or minor stroke will be included over one calendar year

Disqualifiers

There are no exclusion criteria

Ischemic stroke

Intracerebral hemorrhage

Cerebral venous thrombosis

Trial design

Treatments tested in this trial

  • Supported, women-centred and aphasia-friendly recruitment process (ORDERed)
  • Traditional recruitment processes (TRADITIONAL)

Treatment groups

1,600 Participants
are divided into 2 treatment groups

Sponsors and collaborators