Trial of Enhanced Pre-Consent Discussion
Completed · Not applicable
Conditions studied: Pediatric Crohn's Disease
In brief
Nested within the COMBINE pragmatic clinical trial, the investigators will conduct a cluster randomized controlled trial to determine whether, in parents (of children with Crohn's Disease) or patients \> 18 years old being approached for trial participation, a pre-consent discussion enhanced with decision aids is more effective than the standard pre-consent discussion in transferring knowledge to parents/patients related to trial participation.
Key facts
- Study ID
- NCT02869880
- Run by
- Children's Hospital Medical Center, Cincinnati
- People needed
- 241
- Starts
- 2016-10-01
- Expected to finish
- 2019-07-01
- Last updated by the study team
- 2020-01-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Parent of a child who is eligible for the COMBINE trial (ClinicalTrials.gov Identifier: NCT02772965)
- Patient who is eligible for the COMBINE trial (ClinicalTrials.gov Identifier: NCT02772965)
You may not qualify if…
- Non-English speaking
Where it is running
- Cincinnati Children's Hospital Medical Center — Cincinnati, Ohio, United States
Full record on ClinicalTrials.gov
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