Back to search

Article

Patient reported outcomes and recruitment rates following the introduction of principled patient information leaflets (PrinciPILs): Protocol for a meta-analysis

2023-05-26

Abstract excerpt

<h4>Background: </h4> The way potential benefits and harms of trial interventions are shared within patient information leaflets (PILs) varies widely and may cause unnecessary harms (“nocebo effects”). The aim of this meta-analysis will be to evaluate the influence on recruitment rates and early effects on patient reported adverse events of principled patient information leaflets (PrinciPILs) compared with standar...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
f8f6a9c6-e3fd-5c8c-990e-67cf4cccd943
DOI
10.3310/nihropenres.13420.1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Patient reported outcomes and recruitment rates following the introduction of principled patient information leaflets (PrinciPILs): Protocol for a meta-analysisDOI 10.3310/nihropenres.13420.1
Guidance for reporting clinical trial registry records and published protocols use in systematic reviews of interventionsSemantic proximity
The effectiveness of digital multimedia presentation of trial information on recruitment and retention of patients: Protocol for a study within a trial (SWAT).Semantic proximity
Informed consent in randomised controlled trials: further development and evaluation of the Participatory and Informed Consent (PIC) measureSemantic proximity
PROTOCOL: LLM-Generated CONSORT Report for Increased Reporting: A Parallel-Arm Randomized Controlled TrialSemantic proximity
Trial Forge Guidance 5: ethical considerations in randomised Studies Within A Trial (SWATs)Semantic proximity
Development of a Risk-tailored Approach and Dashboard for Efficient Management and Monitoring of Investigator-Initiated TrialsSemantic proximity
Methodological review to develop a list of bias items for adaptive clinical trials: Protocol and rationaleSemantic proximity
Exploring scalable assessment methods for terminated trials in ClinicalTrials.gov: A cohort analysis of German and Californian trialsSemantic proximity
The development of a set of key points to aid clinicians and researchers in designing and conducting n-of-1 trialsSemantic proximity
Development process of consensus-driven SPIRIT and CONSORT extensions for early phase dose-finding trials: the DEFINE (DosE FIndiNg Extensions) studySemantic proximity
Approaches and experiences implementing remote, electronic consent at the Leeds Clinical Trials Research UnitSemantic proximity
[How can we find, design, evaluate and use clinical practice guidelines?].Semantic proximity
Select a neighboring publication to make it the new centre.