Related Experiment Video
Updated: May 20, 2026

E-Patient Counseling Trial (E-PACO): Computer Based Education versus Nurse Counseling for Patients to Prepare for Colonoscopy
Published on: August 1, 2019
Communicating Time-to-Event Treatment Effects in Randomized Trials: A Randomized Experiment among General
Helge Giese1,2, Wolfgang Gaissmaier2, Oliver Kuss3,4
1Heisenberg Chair for Medical Risk Literacy and Evidence-based Decisions, Charité- Universitätsmedizin Berlin, Berlin, Germany.
General practitioners struggle to interpret time-to-event treatment effects from clinical trials, regardless of presentation format. New strategies are needed to effectively communicate these complex outcomes for better patient decision-making.
Area of Science:
- Clinical Trials
- Medical Communication
- Health Outcomes Research
Background:
- Time-to-event outcomes in randomized controlled trials (RCTs) are frequently presented in ways that obscure how treatment effects change over time.
- This lack of clarity hinders clinicians' interpretation of trial results and their ability to support patient decision-making.
Purpose of the Study:
- To evaluate the understanding and acceptability of different formats for communicating time-to-event treatment effects among general practitioners.
- To determine if providing baseline risk information improves the interpretation of these effects.
Main Methods:
- An online experiment was conducted with 250 German general practitioners in April 2024.
- Participants assessed treatment effects using four common formats: hazard ratios, prolongation of life, restricted mean survival time (RMST), and absolute risk reduction.
- Understanding was measured by the ability to compare effect sizes (small, medium, large), and acceptability of each format was also assessed.
Main Results:
- Effectiveness ratings did not differ across formats for distinguishing between small, medium, and large treatment effects.
- Restricted mean survival time (RMST) presentations were rated as less effective but more acceptable compared to other formats.
- The inclusion of baseline risk information did not significantly impact effectiveness ratings or acceptability.
Conclusions:
- General practitioners experienced difficulties interpreting time-to-event treatment effects across all evaluated formats.
- No tested format facilitated an accurate understanding of effect size, even though RMST was preferred.
- Current methods for communicating time-to-event outcomes may be inadequate for clinical practice, necessitating the development of improved strategies.
Related Concept Videos
Randomized Experiments
Simple randomization
Simple...
What is an Experiment?
Hazard Ratio
For example, in a clinical trial evaluating a...
Blinding
Comparing the Survival Analysis of Two or More Groups
Clinical Trials
There are four phases in a clinical trial. A phase one...
