Child health: evidence-informed guidelines Not Applicable
Conditions
Interventions
Study 1. Randomised controlled trial
Participants will be randomly allocated to receive the following ?graded-entry? evidence summary formats.
A = Technical reviews + Systematic reviews (TR+SR)
B =
Sponsors
The Wellcome Trust (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Participants will consist of a purposive sample of technical experts, practitioners and policy makers gathered to develop consensus guidelines during a planned 1 week neonatal stakeholder workshop.
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study 1. Randomised controlled trial We will measure the impact of graded-entry evidence packs on participants? understanding of key messages resulting from the evidence (tracer topic) summaries e.g. issues around persistent dilemmas on the timing (?early? or ?delayed?) and rate of advancement (?rapid? or ?slow?) of feeding volumes in prematurely born sick infants. Study 2. Descriptive case study Data collection will focus on documenting processes involved in knowledge exchange and in the application of GRADE grid in guideline development. Emerging themes following the application of GRADE grid will be presented to all the participants for further discussions to promote consensus on draft essential newborn care (ENC) recommendations. | — |
Secondary
| Measure | Time frame |
|---|---|
| We will measure the impact of graded-entry evidence packs on participants? rating of their experience / satisfaction with the use of provided evidence packs. Rating will be done using a 5-point Likert scale tool (used successfully in previous studies measuring 3 domains of their experience: usability (ease of use as indicated by average time spent looking for information), practical value (e.g. in tailoring research evidence) and barriers to use of evidence pack (accessibility). | — |
Countries
Kenya
Outcome results
None listed