Clinical Decision-making Clinical Trial
— RANKOfficial title:
Review and Assessment of Network Meta-analyses for Knowledge Uptake (RANK) Study
| NCT number | NCT03283592 |
| Other study ID # | 17-0107 |
| Secondary ID | |
| Status | Withdrawn |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | July 2019 |
| Est. completion date | January 2021 |
| Verified date | April 2019 |
| Source | St. Michael's Hospital, Toronto |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This randomized controlled trial will assess the interpretability of the rank-heat plot for presenting the results of network meta-analysis in comparison to SUCRA (surface under the cumulative ranking) plots which are suggested to present one of the best ranking statistics.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | January 2021 |
| Est. primary completion date | January 2021 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Clinicians must be accredited to practice in Canada and working (full- or part-time) as a family physician or general internist. Exclusion Criteria: - Unable to read and understand English; - No access to the internet; - Read, co-authored or peer-reviewed the study: "Quality Improvement strategies to Prevent Falls in the Elderly: A systematic review and network meta-analysis" (manuscript in preparation). |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| St. Michael's Hospital, Toronto |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Proportion of participants who appropriately define the clinical "bottom line." Participants' answers will be independently evaluated by two investigators for agreement with an expert panel's recommendation. | during experiment via single session, <1 hour survey | ||
| Secondary | Proportion of participants who accurately apply the evidence to the provided clinical scenario. | during experiment via single session, <1 hour survey | ||
| Secondary | Completeness of survey data evaluated by two independent investigators | Immediate post-experiment | ||
| Secondary | Time taken to complete survey | Immediate post-experiment |
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