N/A
Completed N=184
Impact of Anticipated Regret Incorporation Into Patient Decision Aids
Regret
Source: ClinicalTrials.gov NCT02563808 ↗
Enrolled (actual)
184
Serious AEs
0.0%
Results posted
May 2019
Primary outcomePrimary: Difference in Consideration of Regret — 62; 69 participants reported regret played role
Summary
The purpose of this study is to investigate the impact of incorporating "anticipated regret " into standard patient decision aids. Participants in the Wharton Behavioral Lab will be administered a standard patient decision aid and an "anticipated regret" augmented decision aid. Participants will complete a computerized survey about their experiences with each version, and their answers will be assessed for potential differences associated with the incorporation of "Anticipated Regret."
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Difference in Consideration of Regret |
62; 69 | — |
Eligibility Criteria
Inclusion Criteria
- Healthy females ages 18 years or older
Exclusion Criteria
- Under age 18 years
Data sourced from ClinicalTrials.gov (NCT02563808). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.