Contamination in complex healthcare trials:the falls in care homes (FinCH) study experience [PDF]
BACKGROUND: Trials are at risk of contamination bias which can occur when participants in the control group are inadvertently exposed to the intervention.
Allen, F +8 more
core +1 more source
BackgroundPeople with cancer often have unidentified symptoms and social care needs. The Needs Assessment Tool-Cancer (NAT-C) is a validated, structured method of assessing patient/carer concerns and prompting action, to address unmet need.AimsAssess ...
Joseph Clark +9 more
doaj +1 more source
Determining the sample size for a cluster-randomised trial: Bayesian hierarchical modelling of the ICC estimate [PDF]
In common with many cluster-randomised trials, it was difficult to determine the appropriate sample size for the planned trial of the effectiveness of a systematic voiding programme for post-stroke incontinence due to the lack of a robust estimate of the
Leathley, Michael John +4 more
core +1 more source
Ethical implications of excessive cluster sizes in cluster randomised trials [PDF]
The cluster randomised trial (CRT) is commonly used in healthcare research. It is the gold-standard study design for evaluating healthcare policy interventions. A key characteristic of this design is that as more participants are included, in a fixed number of clusters, the increase in achievable power will level off.
Karla Hemming +4 more
openaire +3 more sources
The Diabetes Remission Clinical Trial (DiRECT): protocol for a cluster randomised trial [PDF]
Background: Despite improving evidence-based practice following clinical guidelines to optimise drug therapy, Type 2 diabetes (T2DM) still exerts a devastating toll from vascular complications and premature death.
Adamson, Ashley +19 more
core +3 more sources
Activities to support the implementation of complex interventions as part of routine care: a review of the quality of reporting in cluster randomised controlled trials [PDF]
Objective: To review a sample of cluster randomised controlled trials and explore the quality of reporting of (1) enabling or support activities provided to the staff during the trial, (2) strategies used to monitor fidelity throughout the trial and (3 ...
Boutron +17 more
core +2 more sources
The optimal design of stepped wedge trials with equal allocation to sequences and a comparison to other trial designs. [PDF]
Background/Aims We sought to optimise the design of stepped wedge trials with an equal allocation of clusters to sequences and explored sample size comparisons with alternative trial designs.
Copas, Andrew +3 more
core +2 more sources
Data for Thinking Healthy Programme Pakistan trial (THPP-Pakistan) [PDF]
An anonymised dataset of 570 women (one row per woman) who gave informed consent to participate in a cluster randomised, parallel, superiority, controlled trial in Rawalpindi, Pakistan in 2014-2017. The intervention was an adapted version of the Thinking
Ahmad, Ikhlaq +7 more
core +1 more source
Background Early interventions proved to be able to improve prognosis in acute stroke patients. Prompt identification of symptoms, organised timely and efficient transportation towards appropriate facilities, become essential part of effective treatment.
Lori Giuliano +4 more
doaj +1 more source
Background General medical practitioner (GP) recruitment and subsequent data collection in clinical practice are challenging and may limit successful completion of a large-scale trial.
Hazel J. Jenkins +7 more
doaj +1 more source

