Skip to main content
Clinical Trials/NCT04745897
NCT04745897CompletedNot Applicable

Comparing the Accessibility of the World Health Organization's Tuberculosis Guidelines to the eTB Catalogue of Recommendations: A Two-Arm Superiority Randomized Controlled Trial

McMaster University1 site in 1 country244 target enrollmentStarted: February 26, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
244
Locations
1
Primary Endpoint
Accessibility of Information on a Seven-Point Likert Scale

Study Overview

Brief Summary

The World Health Organization's Global Tuberculosis Programme (WHO-GTB) issues evidence-informed guideline recommendations on tuberculosis (TB). These recommendations are used by decision-makers, guideline developers and other stakeholders. In an effort to improve the accessibility and usability of these recommendations, a new eTB catalogue of recommendations has been developed. This study aims to compare the accessibility of the new eTB catalogue to the earlier method of accessing recommendations directed through the general WHO website.

Detailed Description

This is a two-arm superiority randomized controlled trial. The primary objective is to compare the accessibility of information between the eTB catalogue (intervention) and WHO TB (comparison). Secondary outcomes include understanding of the information, satisfaction of catalogue presentation, and preference toward the catalogue. Current and potential users of TB recommendations will be recruited. Data will be collected using a survey with demographic questions and subsequent 1:1 randomization to the intervention. Superiority will be declared if the mean difference in accessibility is 0.5 or greater for the intervention arm on the seven-point Likert scale.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Stakeholders who consider themselves to be users or potential users of tuberculosis (TB) recommendations will be eligible for participation. For the purposes of this trial, a user is defined as someone who has previously accessed TB guidelines, recommendations or policy advice, and a potential user is someone who plans to access TB guidelines, recommendations, or policy advice in the future.
  • •Participants may be part of any group that has a stake in TB, including the public, healthcare providers, policymakers, or researchers. Participants may be from either low- and middle-income countries (LMIC) or high-income countries (HIC).
  • •They may also vary in levels of education and previous TB work experience.

Exclusion Criteria

  • •Individuals involved in eTB catalogue development.

Arms & Interventions

eTB Catalogue of Recommendation (eTB)

Experimental

New eTB catalogue of recommendations website (eTB).

Intervention: eTB Catalogue of Recommendations (eTB) (Other)

World Health Organization Tuberculosis Website (WHO TB)

Active Comparator

Current method of accessing tuberculosis (TB) recommendations using World Health Organization (WHO) website (WHO TB).

Intervention: World Health Organization Tuberculosis Website (WHO TB) (Other)

Outcomes

Primary Outcomes

Accessibility of Information on a Seven-Point Likert Scale

Time Frame: Duration of survey (approximately 10 minutes)

The primary outcome is the accessibility of information on the eTB catalogue compared to the current WHO TB guidelines. Accessibility is defined as the ability to access and use information. This outcome considers the four following domains: (1) how easy is it to find the information (2) how easy is it to understand the information (3) whether the presentation of this information facilitates decision-making (4) overall accessibility of information. These domains will be measured using a seven-point Likert scale (1 = strongly disagree, 7 = strongly agree). The statements will be: 'It was easy to find the information', 'it was easy to understand the information', 'the information was presented in a way that would help me make a decision', and 'this website was easy to navigate'. The investigators will calculate mean composite values of these four domains for the primary outcome of accessibility, and present the four individual domains as secondary outcomes.

Secondary Outcomes

  • Satisfaction on a Seven-Point Likert Scale(Duration of survey (approximately 10 minutes))
  • Preference on a Seven-Point Likert-Scale(Duration of survey (approximately 10 minutes))
  • Understanding with Multiple Choice Questions(Duration of survey (approximately 10 minutes))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials