Skip to main content
Clinical Trials/NCT06972667
NCT06972667Active, not recruitingNot Applicable

Interventions to Decrease Cancer Information Avoidance

State University of New York at Buffalo1 site in 1 country1,500 target enrollmentStarted: December 10, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
1,500
Locations
1
Primary Endpoint
Strength of screening intentions

Study Overview

Brief Summary

Health information avoidance is an overlooked threat to the reach and effectiveness of health communication. To fully realize the benefits of our sizeable investments in health messaging, it is necessary to identify strategies for reducing health information avoidance. The researchers will test a video-based strategy for promoting colorectal cancer screening designed to reduce defensive colorectal cancer information avoidance and increase message reach by increasing engagement among those who would otherwise avoid the message. The researchers will conduct a randomized controlled trial (RCT) comparing the effects of the intervention video to an attentional control video on colorectal cancer screening intentions and uptake.

Detailed Description

The study will test the efficacy and mediating mechanisms of brief video interventions including elements demonstrated to be effective in reducing health information avoidance (self-efficacy boosting, humor, calm affect induction). It is expected that the videos to benefit people who typically avoid health information yet still be beneficial for people who do not avoid health information, thus being suitable for dissemination to general audiences. It is hypothesized that the interventions will strengthen intentions to be screened, increase colorectal cancer risk information seeking and increase screening.

Following recommended practices, the two intervention arms and the control arm will include multiple versions of the videos to control for actor effects. All intervention videos operationalize the same psychological mechanisms but are delivered by 4 different actors and promote either colonoscopy or stool tests. The 8 parallel intervention and 4 control videos will be treated as random effects.

The intervention videos will be tested in members of the Ipsos panel who are not adherent to colorectal cancer screening guidelines, half of whom will be selected because they tend to avoid colorectal cancer information. Effects of the intervention videos will be compared to those of an attentional control video about food safety.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
45 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •between the ages of 45 and 75 years
  • •never diagnosed with colorectal cancer
  • •non-adherent to colorectal cancer screening guidelines
  • •half will have a score at or greater than the mid-point on the colorectal cancer information avoidance scale (≥2.5) on the pre-screening survey such that half of the sample are people who tend to avoid colorectal cancer information

Exclusion Criteria

  • •not between the ages of 45 and 75 years
  • •have been diagnosed with colorectal cancer
  • •adherent to colorectal cancer screening guidelines

Arms & Interventions

Video to promote colonoscopy

Experimental

Participants will view a brief video promoting colonoscopy with self-efficacy enhancement, humor and calm affect induction

Intervention: Video to promote colonoscopy (Other)

Video to promote screening for colorectal cancer with home tests

Experimental

Participants will view a brief video promoting colorectal cancer home testing with self-efficacy enhancement, humor and calm affect induction

Intervention: Video to promote screening for colorectal cancer with home tests (Other)

Attentional control video

No Intervention

The attentional control video will be about food safety and will be the same length and include the same actors and music.

Outcomes

Primary Outcomes

Strength of screening intentions

Time Frame: Day 1

Participants will rate their intention to be screened with the item, "I intend to get checked for colon cancer within the next 6 months" on a scale from 1 to 4 with 4 being stronger intentions.

Strength of intentions to talk to a health care provider about being screened for colorectal cancer

Time Frame: Day 1

This outcome will be assessed with the item, "I will talk to a health care provider about getting checked for colon cancer within the next 6 months".

Proportion of participants who seek personal risk information

Time Frame: Day 1

Participants will be asked whether they want to be redirected at the end of the study to complete the online Siteman Cancer Center colorectal cancer risk calculator.

Proportion of participants screened for colorectal cancer after 9 months

Time Frame: At least 9 months after start of study

The researchers will assess whether participants have been screened for colorectal cancer in the 9 months since participating in the intervention phase of the study.

Secondary Outcomes

  • Positive and negative affect(Day 1)
  • Self-efficacy for colorectal cancer screening(Day 1)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Heather Orom

Principal Investigator

State University of New York at Buffalo

Study Sites (1)

Loading locations...

Similar Trials

Interventions to Decrease Health... | Clinical Trial