Faith in Action! A Church-Based Navigation Model to Increase Breast Cancer Screening in Korean Women

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age45-80
SponsorCedars-Sinai Medical Center

About this trial

The purpose of this research is to develop a culturally adapted "Faith in Action!" curriculum to train lay health navigators to provide breast cancer screening navigation to Korean American women within faith-based settings and evaluate whether the culturally adapted "Faith in Action!" curriculum increases adherence to breast cancer screening guidelines among Korean American women within faith-based settings in Los Angeles, California. The primary research procedures include trainings and key informant interviews with lay health navigators in faith-based settings followed by a cluster randomized trial to evaluate the intervention.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Korean woman who is 45 years or older

Does not currently have a breast cancer diagnosis

Non-adherent to cancer screening (did not receive mammogram in last 2 years based on self-report)

Prospective or current member of participating Korean Churches

Disqualifiers

Does not meet inclusion criteria as described above

Trial design

Design model

Parallel

Treatments tested in this trial

  • Faith in Action! Church-based Navigation Model

    Behavioral

    Cancer screening education and navigation by identified trained navigators in faith based settings + American Cancer Society Screening Guidelines pamphlet

  • Control

    Other intervention

    Presentation on healthy behaviors (physical activity, nutrition) + American Cancer Society Screening Guidelines pamphlet

Treatment groups

320 Participants
are divided into 2 treatment groups
Group A: Faith in Action!Experimental treatment 1 intervention
Group B: ControlActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Screening adherence

Percent change in adherence to breast cancer screening guidelines within 6 months from end of program

Time frame
up to 6 months from end of program

Secondary outcomes

1

Breast Cancer Screening Beliefs (Knowledge, Perception, and perceived risk)

Assessed in validated, Breast Cancer Screening Beliefs Questionnaire (Kwok et al) including Likert-type questions (13 items and 3 sub scales, items range 1-5, strongly agree to strongly disagree)

Time frame
up to 6 months
2

Participant knowledge, attitudes, and beliefs towards screening (Qualitative)

Assessed in qualitative interviews

Time frame
up to 6 months
3

Change in Knowledge of Breast Cancer Screening

Knowledge of breast cancer screening based on pre-post knowledge assessments adapted Cancer 101 assessments (3 knowledge assessments (5 items each), response categories: Agree, Disagree, or Unsure).

Time frame
up to 6 months

Other outcomes

1

Change in NIH PROMIS Global Health

Change in continuous NIH PROMIS converted T-Scores (mean 50, SD:10) at 6 months. Questionnaire includes physical and mental health domains (4 items total, likert 5-point scale, converted to continuous T scores)

Time frame
Up to 6 months

Sponsors and contacts

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Cedars-Sinai Medical Center

Lead sponsor

California Breast Cancer Research Program

Collaborator