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Interactive Tool for Informed Consent

NCT02332837 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2021-03-23

No results posted yet for this study

Summary

Online trials require informed consent from participants. Massive online trials make face-to-face signed consent unrealistic and existing consent comprehension could be improved to increase participant safety and understanding.

This trial will compare understanding of traditional digital consent with multi-media consent and with consent that is multi-media and interactive and uses a test and train model.

The computer will assign participants to 1 of 3 methods to present online consent to participants

Conditions

  • Informed Consent

Interventions

BEHAVIORAL

Intervention A: Questionnaire accuracy

Participants will be tested by questionnaire to measure how well consent is understood

BEHAVIORAL

Intervention B: Questionnaire speed of completion

Time to complete questionnaire from time of presentation

BEHAVIORAL

Intervention C: Questionnaire Completion rate

Number of participants who complete the questionnaire

Sponsors & Collaborators

  • ThinkWell

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-31
Primary Completion
2019-11-30
Completion
2020-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02332837 on ClinicalTrials.gov