Sample size and power training for use in clinical trials

Webinar

Sample Size for Pilot Studies

 

Maximising the Value of Pilot Data

This webinar has ended

Watch Now

About the webinar

Pilot Studies are a common strategy to assess the feasibility of a study by previewing the expected outcome in a larger study. However, pilot studies are often too small and may often lead to suboptimal decision making at the trial design stage.

For example, insufficiently sized pilot studies may significantly mis-specify the pre-trial estimates for the effect size or nuisance parameters used in a study’s sample size determination.

In this webinar we explore the impact of sample size on pilot study performance, look at the validity of common rules of thumb for pilot size and more formal approaches for sizing pilot studies appropriately.

In this free webinar, we will cover:

              • An Introduction to Pilot Studies

              • Common Rules of Thumb for Pilot Study Size

              • Sample Size Determination for Pilot Studies
            • Internal Pilot for Blinded Sample Size Re-estimation

More about the webinar

 

Pilot study sample sizes are often based on simple rules of thumb such as the “rule of 30”. However, these heuristics have been evaluated to be inadequate to achieve the goal(s) of interest for a pilot study. Newer methods allow for the pilot study sample size to be calculated which integrate the objectives and design of the pilot study.

 

In addition, blinded adaptive design provides an approach where a pilot study can be directly integrated into the full study. This improves power and ensures the pilot data can be easily utilised in the final analysis. For example, the internal pilot design for sample size re-estimation can adjust for over-optimism in the estimates for nuisance parameters such as the variance or overdispersion at the planning stage.

 

Join us for this webinar as we explore the impact of sample size on pilot study performance, look at the validity of common rules of thumb for pilot size and more formal approaches for sizing and integrating pilot studies.

 

Duration - 60 minutes

Speaker: Ronan Fitzpatrick, Lead Statistician, nQuery

Watch Now

All info submitted is secure. View our privacy policy.


About Our Host

Ronan Fitzpatrick

Ronan Fitzpatrick - nQuery Head of Statistics - Circle Image

 

nQuery
Lead Statistician

Reducing the risk & cost of clinical trials, for innovative organizations such as:
Sanofi-updated-grey
worldwide-clinical-trials
Covance-G_Logo
quintiles_logo_2017_grey
FDA_G_Logo
AstellasG_Logo
celgene_logo_download
Boehringer_Ingelheim_Logo-png-updated
PRA_Health_Sciences
Astrazeneca logo
Amgen_G_Logo
Novartis_G_Logo
abbvie-logo-updated_tmp15240
Merck_GLogo
Biogen-updated-logo
Ipsen-logo-only
Eli_Lilly_and_Company-G_Logo
Is there someone in your network that would be interested in our webinar?
Share this page by clicking below.