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OpenTrials
Completed

NCT Number: NCT05956353

Stories for Change: Early Detection Can Save Lives

The purpose of this study is to evaluate the Stories for Change (S4C) Cancer Prevention digital storytelling intervention for acceptability and socio-behavioral constructs to increase cancer screening among Hispanic or Latino individuals.

Completed

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Key information

Conditions

Prevention

Age range

21 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Moutain Park Health Center, Phoenix, Arizona, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Self-identify as Hispanic, Latino/a/x/e, or Chicano/a/x;
  • For breast cancer screening: age 40-74 years; for cervical cancer screening: age 21-65 years; for colorectal cancer screening: age 45-75 year
  • Receive primary care at either Hennepin Healthcare (HH) or Mountain Park Health Center (MPHC), or Mayo Clinic.
  • At least one office visit within the previous 12 months to the primary care site.
  • Eligibility for breast, cervical, or colorectal cancer screening documented in the electronic medical record (EMR).
  • Intention to continue to receive medical care at HH, MPHC or Mayo Clinic for the next three months.

If a potential participant is eligible for more than one screening, they will be given the option of participating in multiple versions of the intervention.

Exclusion criteria

  • Individuals with previous breast, cervical, or colorectal cancer diagnoses.
  • For the participants in the colorectal cancer screening intervention, those under surveillance (i.e., did not have a cancer diagnosis but did have polyps) will also be excluded.

Treatment and study plan

Digital Storytelling Intervention

Behavioral

Culturally tailored narrative-based videos created by individuals to promote colorectal, breast and cervical cancer screening among eligible participants in a primary care practice.

Primary outcomes

  1. Number of participants screened and recruited

    Time frame: 1 year

    Our primary measure is the number of participants screened and recruited. We need this information to calculate the number needed to screen in order to recruit one participant from each site in our future randomized controlled trial.

Secondary outcomes

  1. Constructs associated with effective implementation research

    Time frame: 1 year

    Our secondary measure will utilize the Consolidated Framework for Implementation Research. We need this information to identify recruitment successes and opportunities for change in our future randomized controlled trial.

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jul 21, 2023
Registry last updated
Apr 11, 2024

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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