Defining Decision Thresholds for Judgments on Health Benefits and Harms Using the GRADE Evidence to Decision (EtD) Frameworks: Protocol for a Randomized Methodological Study (GRADE-THRESHOLD)
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- McMaster University
- Enrollment
- 1,406
- Locations
- 1
- Primary Endpoint
- Moderate effect of an intervention
Study Overview
Brief Summary
The objective of this study is an approach to derive and use decision-thresholds for judgments on health benefits and harms using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) Evidence to Decision (EtD) frameworks.
Detailed Description
The objective of this study is to derive decision-thresholds (DTs) for Evidence to Decision (EtD) judgments on the magnitude of health benefits and harms. The study hypothesis is that DTs could discriminate between the four categories for EtD judgments. Explicit DTs, providing an indication for which could be the appropriate judgment for a given scenario, might have the potential to support panels of decision-makers in their work, facilitate a common understanding, and promote consistency and transparency in judgments.
Study investigators will conduct a methodological randomized controlled trial to collect the data that allow deriving the decision-thresholds. They will invite clinicians, epidemiologists, decision scientists, health research methodologists, experts in Health Technology Assessment (HTA), members of guideline development groups and the public to participate in the trial. Then, investigators will investigate the validity of decision-threshold by measuring the agreement between judgments that were made in the past by guideline panels and the judgments that the DTs approach would suggest if applied on the same guideline data.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- Triple (Participant, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 99 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •The target population of the survey will include:
- •clinicians
- •epidemiologist
- •decision scientists
- •health research methodologists
- •experts in health technology assessment (HTA)
- •and members of guideline working groups
- •members from the general public
Exclusion Criteria
- •Prior participation in the survey
Arms & Interventions
Threshold estimates
Descriptive case-scenarios
Intervention: descriptive case-scenarios (Other)
Alternative threshold estimates
Descriptive case-scenarios
Intervention: descriptive case-scenarios (Other)
Outcomes
Primary Outcomes
Moderate effect of an intervention
Time Frame: immediate after completion of study
Questionnaire:Participants will be asked to indicate which decision threshold for discriminating between EtD judgments of 'Small' and 'Moderate' they felt appropriate at the time of participation in the survey.
Small effect of an intervention
Time Frame: immediate after completion of study
Questionnaire: Participants will be asked to indicate which decision threshold for discriminating between EtD judgments of 'Trivial or None' and 'Small' they felt appropriate at the time of participation in the survey.
Large effect of an intervention
Time Frame: immediate after completion of study
Questionnaire:Participants will be asked to indicate which decision threshold for discriminating between EtD judgments of 'Moderate' and Large' they felt appropriate at the time of participation in the survey.
Secondary Outcomes
No secondary outcomes reported
