Clinical Trials Directory

Trials / Terminated

TerminatedNCT01994447

The Train Study: Parental Understanding of Informed Consent

"Traditional Research Nurses Versus an Innovative Undergraduate Research Assistant Program: Parental Understanding of Informed Consent " (the TRAIN Study)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
University of Calgary · Academic / Other
Sex
All
Age
14 Years
Healthy volunteers
Accepted

Summary

Project Summary: One of the challenges facing pediatric researchers is the need to balance decreasing funding with the time and human resource costs associated with enrolling children. In order to address this, the Emergency Department (ED) research team developed an innovative model for subject enrollment and consent using highly trained and supervised undergraduate students. From a human resources perspective, utilizing students is more cost effective than the traditional research nurse model. However, a concern with this method is the adequacy of parental understanding of study information for informed consent. The aim of this project is to determine if the use of students is at least as good as the more costly "gold standard" of experienced research nurses. The validation of this innovative student model will enable child health investigators to better meet parent's needs and increase the efficiency of pediatric research. The primary objective of this study is to measure parental comprehension of informed consent information using an innovative undergraduate research assistant program compared to consent using the traditional research nurse model. We hypothesize that parental comprehension of the informed consent information process when approached by undergraduate students will be comparable (or not worse) than when consent is obtained by a research nurse.

Conditions

Interventions

TypeNameDescription
OTHERStudent EnrollmentThe standard informed consent process is for research nurses to provide verbal explanations of studies. In the intervention arm trained research students will use DVD's made by the studies principal investigator to explain study information in the informed consent process.

Timeline

Start date
2013-11-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2013-11-25
Last updated
2016-10-26

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01994447. Inclusion in this directory is not an endorsement.