Utilizing Advocates and Supporters to Increase Lung Cancer Screening Rates in Eligible Participants

Breast Carcinoma Clinical Trial

Official title:

Utilizing Spheres of Influence to Increase Cancer Screening: Empowering Community Health Advocates

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05978128
• Other study ID #: 22-000947
• Secondary ID: NCI-2023-04133
• Status: Recruiting
• Phase: N/A
• Start date: July 28, 2023
• Est. completion date: September 30, 2029

Study information

• Verified date: October 2023
• Source: Jonsson Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical trial assesses the use of advocates and supporters of breast and lung cancer screening to increase lung cancer screening rates amongst eligible participants. Imaging-based cancer screening is utilized with variable frequency. Breast cancer screening with mammography has been widely accepted and is commonly used among eligible women. Lung screening with computed tomography scans is poorly used, despite the potential to decrease deaths from lung cancer. There are many reasons lung screening isn't being used when compared to breast screening, such as smoking stigma and fear, along with a lack of awareness of lung screening. By conducting this trial, researchers want to assess the effectiveness of advocates and supporters of breast and lung screening, and to learn about the psychological barriers to cancer screening, identifying those that are unique to lung screening.

Description:

PRIMARY OBJECTIVES:

I. Determine the number of patients undergoing breast screening who are eligible to participate in lung screening.

II. Determine whether patients currently participating in cancer screening (breast OR lung) are successful as "cancer screening advocates." III. Determine whether laypersons who are aware of screening (including those who accompany friends and family members to their screening appointments) are successful as "cancer screening advocates." IV. Identify knowledge base and psychological barriers to screening through surveys of potential screening participants.

OUTLINE:

Participants access an electronic patient portal with educational materials at baseline, 1- and 2-year follow-ups, and also interact with a patient navigator on study. Patients also receive materials to share with their friends/family on benefits of breast and lung cancer screening on study.

After completion of study intervention, participants are followed up yearly for up to 3 years.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 800
• Est. completion date: September 30, 2029
• Est. primary completion date: September 30, 2028
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Age:

• Breast screening > 40

• Lung screening 50-80

• Male (M) or Female (F)

• Current, former, or never smokers

• Close family or friend with smoking history (in or out of state)

Exclusion Criteria:

• Age:

• Breast screening < 40

• Lung screening < 50 or > 80

• Persons who had previously received a diagnosis of lung cancer, had hemoptysis, or had an unexplained weight loss of more than 6.8 kg (15 lb) in the preceding year will also be excluded

• Persons with an active cancer

Related Conditions & MeSH terms

• Breast Carcinoma
• Breast Neoplasms
• Carcinoma
• Lung Carcinoma

Intervention

Behavioral:
• Health Education
Access electronic patient portal with educational material

Other:
• Health Promotion and Education
Receive materials on breast/lung cancer screening

Behavioral:
• Patient Navigation
Interact with a patient navigator

Other:
• Survey Administration
Ancillary studies

Locations

Country	Name	City	State
United States	UCLA / Jonsson Comprehensive Cancer Center	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
Jonsson Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Increased rates of lung and breast cancer screening adherence	By following up with patients over the defined study period and assessing whether they obtained an incidence screen completed at one-year +/- 3 months from the recommended time. Will also measure the rates of survey completion by consented participants, the number of clicks and time spent reviewing educational materials, and the number of new participants who contacted the program through a referral by another participant.	Up to 3 years
Secondary	Success of "sphere of influence" model	Considered successful if increased lung cancer screening referrals are a direct result of women receiving screening mammograms inviting and educating friends and family about lung cancer screening.	Up to 3 years