Patient Reported Outcomes Burdens and Experiences (PROBE) - Phase 3 - Longitudinal Data Collection

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The PROBE Phase-3 study will collect data on patient reported outcomes, burdens, and experiences in patients living with hemophilia. The investigators will perform comparisons among countries, within country over time, within country against national normative data.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• PWH will be recruited through national hemophilia patient organizations utilizing their existing membership rosters, social media outlets and meetings / events. The investigators are not proposing a pre-determined method of PWH recruitment. They will utilize the information acquired in the workshop and take-home project to inform best practice in recruitment methodology for the study. The investigators may consider requesting different countries test different PWH recruitment strategies to test reproducibility.

⁃ In the future, the questionnaire might also be administered to patients with other chronic conditions.

Locations
Other Locations
Canada
McMaster University
RECRUITING
Hamilton
Contact Information
Primary
Mark Skinner
mskinnerdc@gmail.com
202.253.8342
Backup
Alfonso Iorio
iorioa@mcmaster.ca
Time Frame
Start Date: 2018-01-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 1000
Related Therapeutic Areas
Sponsors
Collaborators: Patient Outcomes Research Group (PORG), National Hemophilia Foundation
Leads: McMaster University

This content was sourced from clinicaltrials.gov