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OpenTrials
Completed

NCT Number: NCT05275361

Utilizing Social Contacts to Facilitate Mammogram Screening Among African American Women

Eliminating racial disparities in breast cancer is a top public health priority. African American (AA) women often present with more advanced and aggressive disease at the time of diagnosis and are more likely to die from breast cancer than any other racial/ethnic group in the United States. Mammogram screening significantly reduces breast cancer mortality by diagnosing cancer at an earlier stage where treatments are more effective. While some AA women do not schedule screening mammograms as recommended by current guidelines, others do not show up for their exams after scheduling them (no-shows). No-shows to cancer screening appointments impose an enormous strain on our limited healthcare resources with negative impact on other patients who could have secured earlier appointments, loss of revenue for hospitals or clinics serving underserved populations and delays in diagnoses and treatment for those who do not have screening. The investigators identified a high no-show rate for screening mammograms at our hospital. AA women were almost three times more likely to no-show for their mammograms compared to White women. Patient's social networks plan an important role in health promotion. In this study, we will pilot an intervention involving patient's social contacts (family, friends, neighbors, etc.) as healthcare facilitators to improve appointment attendance. The investigators seek to determine whether this intervention is feasible and acceptable to patients and whether this intervention will improve attendance rates for screening mammograms among AA women at our institution. If effective, the use of a patient's social contact person as a healthcare facilitator (similar to a patient navigator) would be a readily available and inexpensive resource for other institutions to implement.

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Key information

Age range

40 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

for Patients:

  • Female
  • African American
  • At least 40 years old
  • Scheduled for a screening mammogram within 3 months following initiation of the study
  • Willing and able to provide contact information for two adult social contacts (friends or family members)

Exclusion criteria

for Patients:

-Prior history of breast cancer

Inclusion criteria

for Social Contacts:

  • At least 18 years old
  • Selected by the patient as someone (family member or friend) who would be able to support her in keeping her mammogram appointment

Exclusion criteria

for Social Contacts:

-Less than 18 years of age

Treatment and study plan

Social Contact Reminder

Behavioral

-The social contact will remind patient about screening mammogram appointment

Primary outcomes

  1. Feasibility of recruiting patients' social contacts to serve as healthcare facilitators as measured by number of participants enrolled to the study with a social contact that agrees to participate

    Time frame: Through completion of enrollment (estimated to be 3 months)

    -The study is deemed feasible if 80 participants are enrolled to the study and further, if at least 65% of the 80 participants will have a social contact agreeing to participate

Secondary outcomes

  1. Describe demographic characteristics of the social contacts and any associations with patient appointment attendance

    Time frame: Through mammogram appointment (estimated to be 6 months)

    -Use descriptive statistics to present the characteristics of social contacts and regression analysis to determine in association with social contact characteristics and appointment attendance.

  2. Rate of mammography attendance

    Time frame: Through mammogram appointment (estimated to be 6 months)

  3. Using a structured survey interview, determine the percentage of patients and their social contacts who respond positively (agree or strongly agree) that the intervention helped them keep their scheduled screening mammogram appointment

    Time frame: Through mammogram appointment (estimated to be 6 months)

    -Use descriptive statistics to present response to structured interview questions.

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • American Society of Clinical Oncology

Registry information

Official study title

Pilot Study Utilizing Social Contacts to Facilitate Mammogram Screening Among African American Women

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Mar 11, 2022
Registry last updated
Jul 7, 2022

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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