NCT07854548

Brief Summary

Recommendations from health organizations rest on a scale. On this scale, some recommendations can be "stronger" than others. This "strength" should be easily understood by everyone, including members in the public and healthcare professionals. The survey results will help us find a better way to phrase recommendations.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
741

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

September 1, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
9 months until next milestone

First Posted

Study publicly available on registry

October 2, 2026

Completed
Last Updated

October 2, 2026

Status Verified

August 1, 2026

Enrollment Period

5 months

First QC Date

September 1, 2025

Last Update Submit

September 27, 2026

Conditions

Keywords

wordingstrengthrecommendation

Outcome Measures

Primary Outcomes (1)

  • Understanding of the Strength and Direction of Recommendation

    The primary outcome is understanding of the correct interpretation of recommendation strength and direction. This will be assessed with three multiple-choice questions where answer options represent interpretations for strong-for, conditional-for, conditional-against, and strong-against recommendation statements, as indicated by GRADE. Each question has 1 correct answer. Scores will be assessed per-question and aggregate (maximum score of 3/3 suggesting correct understanding versus minimum 0/3 suggesting poor understanding).

    During a single survey session (approximately 10 minutes)

Secondary Outcomes (2)

  • Intended Behaviour

    During a single survey session (approximately 10 minutes)

  • Preference

    During a single survey session (approximately 10 minutes)

Study Arms (3)

GRADE approach ("recommends" and "suggest")

EXPERIMENTAL

Recommendation statements structured as follows: The guideline panel recommends… The guideline panel suggests…

Other: GRADE approach ("recommends" and "suggest")

New approach ("strongly recommends" and "conditionally recommends")

EXPERIMENTAL

Recommendation statements structured as follows: The guideline panel strongly recommends… The guideline panel conditionally recommends…

Other: New approach ("strongly recommends" and "conditionally recommends")

Alternate approach ("should" and "may")

EXPERIMENTAL

Recommendation statements structured as follows: * should be used * may be used

Other: Alternate approach ("should" and "may")

Interventions

"recommend" (strong) and "suggest" (conditional) Example: The guideline panel recommend(s)/suggest(s) \[against\] \[the intervention\], rather than \[the comparator\], for \[indication\].

GRADE approach ("recommends" and "suggest")

"strongly recommend" (strong) and "conditionally recommend" (conditional) Example: The guideline panel strongly recommend(s)/conditionally recommend(s) \[against\] \[the intervention\], rather than \[the comparator\], for \[indication\].

New approach ("strongly recommends" and "conditionally recommends")

"should" (strong) and "may" (conditional) Example: \[The intervention\] should/may \[not\] be \[verb\], rather than \[the comparator\], for \[indication\]

Alternate approach ("should" and "may")

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Individuals of 16 years or older of age
  • Ability to read and understand English
  • Previous use of, or intention to use, health guidelines or recommendations (e.g., intention to access clinical or public health guidelines, recommendations, or policy advice)

You may not qualify if:

  • Previous participation in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

McMaster University

Hamilton, Ontario, Canada

Location

MeSH Terms

Interventions

GRADE ApproachSuggestion

Intervention Hierarchy (Ancestors)

Patient Outcome AssessmentOutcome Assessment, Health CareOutcome and Process Assessment, Health CareHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationHypnosisMind-Body TherapiesComplementary TherapiesTherapeuticsPsychotherapyBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 1, 2025

First Posted

October 2, 2026

Study Start

August 1, 2025

Primary Completion

December 30, 2025

Study Completion

December 30, 2025

Last Updated

October 2, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data will only be used for purposes of analyses in this study.

Locations