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Comparing Paper-based and Tablet-delivered Informed Consent for Older Adults

NCT02114970 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2016-08-16

No results posted yet for this study

Summary

The investigators will develop and test a tablet-delivered informed consent process. In a preliminary phase of the study, older adults will provide feedback on a prototype tablet-delivered consent by participating in a focus group. In a separate second phase, older adults will be randomly assigned to a tablet-delivered or paper-delivered consent condition in which their comprehension of material covered in the consent will be assessed.

Conditions

  • Tablet-delivered Informed Consent
  • Paper-based Informed Consent

Interventions

OTHER

Randomized- paper consent

OTHER

Randomized- Tablet-delivered consent

OTHER

Focus Group- paper and tablet consent

Sponsors & Collaborators

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Nimali Jayasinghe, Ph.D. · Weill Medical College of Cornell University

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2014-11-30
Completion
2014-11-30

Countries

  • United States

Study Locations

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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 NCT02114970 on ClinicalTrials.gov