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NCT Number: NCT07805083

Community Enhanced Virtual Informed Consent

The goal of this clinical trial is to examine perceptions of virtual human communicators and cancer research recruitment messages. This study will also examine how different informed consent approaches influence decisions to participate in research.

Recruiting

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Key information

Conditions

Hematopoietic and Lymphatic System Neoplasm Malignant Solid Neoplasm

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic in Florida

Jacksonville, Florida, 32224-9980, United States

Location status: Recruiting

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Able to speak, read, or understand English sufficiently to provide informed consent
  • 18 years of age or older
  • White or Black
  • Living in the United States

Exclusion criteria

  • Unable to speak, read, or understand English sufficiently to provide informed consent
  • Inability on the part of the patient to understand the informed consent or be compliant with the protocol

Treatment and study plan

Educational Cancer Intervention

Behavioral

Participants will view informed consent messaging presented in different formats

Other names: Behavioural

ICF Text Version 1

Other

Receive a text-based informed consent form

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

ICF Text Version 2

Other

Receive an adapted text-based informed consent form

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

ICF Video Version 1

Other

Receive a video-based informed consent form delivered by virtual human #1

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

ICF Video Version 2

Other

Receive a video-based informed consent form delivered by virtual human #2

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

ICF Video Version 3

Other

Receive a video-based informed consent form delivered by virtual human #3

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

ICF Video Version 4

Other

Receive a video-based informed consent form delivered by virtual human #4

Other names: Formal Consent, Informed Consent, INFORMED CONSENT OBTAINED

Survey Administration

Other

Ancillary studies

Primary outcomes

  1. Self-efficacy (Aim 1)

    Time frame: Baseline (immediately following intervention)

    Assessed by 3 questions in the study-specific survey. The questions are answered on a scale of 1 (strongly disagree) to 5=strongly agree. Higher scores indicate greater feelings of self-efficacy.

  2. Trustworthiness (Aim 2)

    Time frame: Baseline (immediately following intervention)

    Assessed by a study-specific survey asking participants to rate the intervention on a scale of 1 (untrustworthy) to 7 (trustworthy). Higher scores indicate greater perception of trustworthiness.

Interested in participating?

Recruiting

Interested in participating?

Request Info

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Exploring Health Communication Message Factors That Influence Cancer Research Recruitment

Acronym: CEVIC

Important dates

Study start
2026
Primary completion
2027
Study completion
2029
First posted
Sep 4, 2026
Registry last updated
Sep 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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