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Interactive Informed Consent and Decision Conflict

NCT05980078 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 94

Last updated 2025-07-31

No results posted yet for this study

Summary

Informed consent for surgery can address the legal aspects while also being simple, informative, and empathic. It can help people confirm that the potential harms are acceptable in light of the potential benefits. Standard consent forms just document this process, while a computer-based, interactive consent process can also standardize and potentially enhance it.

Conditions

  • Upper Extremity Problem

Interventions

OTHER

Interactive consent

They were randomized to complete an interactive consent.

OTHER

Standard consent

They were randomized to complete a standard written consent.

Sponsors & Collaborators

  • University of Texas at Austin

    lead OTHER

Principal Investigators

  • David Ring, MD · Professor of orthopedic surgery at The university of Texas at Austin

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2020-03-01
Completion
2023-05-01

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 NCT05980078 on ClinicalTrials.gov