Participant Panel
Cross-source consensus on Participant Panel from 1 sources and 5 claims.
1 sources · 5 claims
Risks & contraindications
Evidence quality
Other
Other
Highlighted claims
- The study retained 82.5% of consenting participants, with 11 of 63 dropping out. — Developing a minimum dataset for a national patient registry on Long COVID in Canada: a Delphi consensus-based study
- The panel included patients, caregivers, clinicians, and researchers from multiple Canadian provinces. — Developing a minimum dataset for a national patient registry on Long COVID in Canada: a Delphi consensus-based study
- The study recruited participants through the Long COVID Web network, word-of-mouth, patient-oriented research groups, and academic institutions across Canada. — Developing a minimum dataset for a national patient registry on Long COVID in Canada: a Delphi consensus-based study
- Only 52 participants completed all three rounds, below the target of 100 but above typical Delphi panel sizes reported in the literature. — Developing a minimum dataset for a national patient registry on Long COVID in Canada: a Delphi consensus-based study
- The participant profile was limited by a skew toward women, limited ethnic and racial diversity, and absence of policymakers or health system decision-makers. — Developing a minimum dataset for a national patient registry on Long COVID in Canada: a Delphi consensus-based study