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Improving Uptake of Genetic Cancer Risk Assessment in African American Women- Video

Improving Uptake of Genetic Cancer Risk Assessment in African American Women- Video

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04476654
Enrollment
57
Registered
2020-07-20
Start date
2021-11-01
Completion date
2023-06-12
Last updated
2024-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

genetic counseling and testing

Brief summary

Genetic counseling and testing (GCT) provides invaluable information for women who are at-risk of hereditary breast and/or ovarian cancer (HBOC). Black women underutilize GCT compared to White women. This study will conduct a RCT to test the efficacy of a culturally-tailored theory-based video intervention aimed to address key psychosocial factors (emotions, ambivalence) to improve uptake of genetic counseling in Black women at increased risk of HBOC. Findings from this study may offer an opportunity to engage at-risk Black women regarding genetic counseling through a multi-center trial and ultimately address the disparity in genetic counseling uptake that exists between Black and White women.

Detailed description

Breast cancer (BC) is the most frequently diagnosed cancer in African American women (hereafter referred to as Black) and their cancer mortality is higher than other racial/ethnic groups in the United States (US). Compared to non-Hispanic Whites, Black women are diagnosed younger and with more advanced breast cancer. When diagnosed with BC, Black women present more often with triple-negative breast cancer (TNBC) an aggressive disease defined by the absence of estrogen and progesterone receptors, and human epidermal growth factor (HER)-2 expression. TNBC has been associated with pathogenic BRCA1 variants. Racial disparities also exist for women with ovarian cancer, the most lethal of the gynecologic cancers. Among women with advanced ovarian cancers up to 21% are associated with inherited pathogenic mutations the most common of which is BRCA1. Women who carry a pathogenic BRCA variant (PV) have a lifetime breast cancer risk of 55-70% and a lifetime ovarian cancer risk of up to 44%. The National Comprehensive Cancer Network (NCCN) recommends referral for Hereditary Breast and Ovarian Cancer (HBOC) genetic counseling and testing (GCT) for women at risk of carrying a BRCA PV. GCT provides women with information needed to make informed decisions to reduce their cancer risk, yet Black women are less likely to use GCT than whites. There is a dearth of interventions to address this issue and produced results are mixed and modest. Awareness of a positive result can inform treatment decisions for cancer patients and risk management in survivors or women unaffected with cancer. Reasons for the lower uptake of GCT in Black women are multi-factorial and include access, knowledge, psycho-social factors, and may vary by cancer status (affected versus unaffected). There are substantial scientific gaps regarding effective interventions to address the sub-optimal uptake of GCT in Black women. To be effective, GCT interventions should be anchored within the needs and cultural values of their audience. While improving knowledge about GCT and one's individual risks is important, interventions that only address knowledge may not enhance uptake, as risk information evokes emotional reactions that are often stronger predictors of behaviors than cognitive factors. Notably, this team has identified factors that contribute to Black women's uptake of GCT. In preliminary studies, researchers found that self-efficacy in making decisions about GCT and medical mistrust were associated with GCT uptake. Low knowledge among Black BC survivors at risk of HBOC has also been found. Anticipated negative emotions to GCT have been associated with lower uptake. Similar studies suggest that Black women report emotions related to fear of being singled out, and the fear of being hopeless. Because most interventions have focused solely on knowledge or access, the proposed study makes a considerable shift in the field by additionally targeting emotions, ambivalence, and developing a media-based risk communication tool. Guided by two evidenced-based theories and preliminary data, this will be a two-phased mixed methods study. In Phase I (months 1-7), formative research and preliminary data will be used to develop the script for the GCT video. The script will be reviewed by GCT experts (n=4) and piloted in two focus groups (n=16) followed by a staged reading to make final refinements. In Phase II (months 8-24), a two-arm randomized trial (RCT) to compare GCT uptake and psycho-social outcomes between 50 at-risk Black women receiving printed Susan G. Komen developed GCT literature (control group) (n=25) or a tailored YouTube video intervention (n=25) will be conducted . All women will be referred to an appointment scheduler who will assist them with making an appointment with a genetic counselor. Participants will complete a baseline survey and follow-up assessment. The primary outcome will be genetic counseling uptake and receipt testing at 3-months will be explored. Specific aims are to: Aim 1. Develop a YouTube video using a formative data for Black women at risk for HBOC. Aim 2. Evaluate the efficacy of the intervention by comparing outcomes between women in the YouTube intervention arm vs. control group arm. H.2.1. Women in the intervention group (vs control group) will have higher genetic counseling uptake. H.2.2. Women in the intervention group (vs control group) will report higher knowledge, higher self-efficacy, higher endorsement of positive attitudes, and positive anticipated emotions about GCT. H.2.3. Most women (≥75%) will be satisfied with the experimental intervention. Enhancing GCT in at-risk populations is a national priority. Given trends towards panel testing and other genomic advances, there is potential for existing disparities to widen. Findings will inform new strategies for behavioral interventions for Black women and a larger trial. If successful, the intervention could be easily disseminated broadening its reach to affected and unaffected women. This study meets the Healthy People 2020 goals to enhance GRCA in at-risk populations, and the national priorities to increase diversity in genetics research participation and incorporate emotions into cancer research. Findings will inform new strategies for behavioral interventions targeting African-Americans in a larger trial.

Interventions

BEHAVIORALYouTube Video Arm

Participants (n=25) will watch a 20 minute YouTube video that will describe the genetic counseling and testing process and risk/benefit information in a culturally relevant format. Participants will complete pre and post assessments. After the session, participants interested in pursuing genetic counseling and testing services will be referred to a patient navigator who will navigate participants to identified no cost or low cost services.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Parallel Assignment

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Must be at least 18 years of age * Must be at high risk for hereditary breast or ovarian cancer * Must identify as Black/African American * Must be a woman * Referred to a genetic counselor for the purpose of being high risk of carrying a hereditary breast and/or ovarian cancer mutation Genetic Counselors: * Must be at least 18 years of age * Must be qualified * Must be approved by the PI

Exclusion criteria

* Under the age of 18 * Race other than Black/African American * Do not gave a high risk for hereditary breast or ovarian cancer Genetic Counselors: * Under 18 * Not qualified * Not approved by the PI

Design outcomes

Primary

MeasureTime frameDescription
Rate of Genetic Counseling and Testing Uptake.3 monthsOur primary outcome will be for participants to receive genetic testing and counseling.Investigators will be able to see if participant has scheduled a genetic testing appointment within the VCU Health appointment system.

Secondary

MeasureTime frameDescription
Knowledge Scale - Genetic Counseling and Testing Knowledge .Baseline was collected up to 48 hours from the start of the intervention and the follow-up was assessed within 48 hours post-intervention.The investigators measured general knowledge about hereditary breast and ovarian cancer. GCT knowledge was ascertained using a 13 item scale developed by Erblich et al.'s (2005). Example items included have you ever heard about genetic counseling for BRCA 1 and 2? and have yes/no or true/false options. Scores across the 13 item Knowledge scale were summed with a range of ( 0-13) where higher values indicated higher knowledge.
Self-efficacy ScaleBaseline was collected up to 48 hours from the start of the intervention and the follow-up was assessed within 48 hours post-intervention.The investigators measured participants self-efficacy in genetic counseling services.Self-efficacy was measured with 3 items on a 5-point likert-scale, with questions that was developed for this study. Example items include how confident are you that you can cope with your risk of developing cancer?. Response options are on a 5-point likert scale ranging from not at all confident (1) and very confident (5). Scores across the 3- item scale were summed with a range of (3-15) where higher scores indicated higher self efficacy.

Countries

United States

Participant flow

Recruitment details

Trained clinical coordinators recruited participants, administered surveys and abstracted information on genetic counseling and testing from participant medical records

Pre-assignment details

The clinical research assistants consented interested patients . Following consent, women completed a baseline survey. Next, women were randomized into study arms.

Participants by arm

ArmCount
Fact Sheet Arm
Komen print materials about genetic counseling and testing will be given to women.
29
YouTube Video Arm
Participants in this arm will receive the culturally tailored video either via a Youtube link or a DVD. YouTube Video Arm: Participants (n=25) will watch a 20 minute YouTube video that will describe the genetic counseling and testing process and risk/benefit information in a culturally relevant format. Participants will complete pre and post assessments. After the session, participants interested in pursuing genetic counseling and testing services will be referred to a patient navigator who will navigate participants to identified no cost or low cost services.
28
Total57

Baseline characteristics

CharacteristicFact Sheet ArmYouTube Video ArmTotal
Age, Continuous47.24 years
STANDARD_DEVIATION 16.91
49.50 years
STANDARD_DEVIATION 13.38
48.35 years
STANDARD_DEVIATION 15.19
Genetic Counseling Knowledge7.69 units on a scale
STANDARD_DEVIATION 1.75
7.50 units on a scale
STANDARD_DEVIATION 1.45
7.60 units on a scale
STANDARD_DEVIATION 1.6
Race/Ethnicity, Customized
Black/African American
29 Participants28 Participants57 Participants
Self-Efficacy to Screen14.38 units on a scale
STANDARD_DEVIATION 1.21
14.29 units on a scale
STANDARD_DEVIATION 2.32
14.33 units on a scale
STANDARD_DEVIATION 1.83
Sex: Female, Male
Female
29 Participants28 Participants57 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Rate of Genetic Counseling and Testing Uptake.

Our primary outcome will be for participants to receive genetic testing and counseling.Investigators will be able to see if participant has scheduled a genetic testing appointment within the VCU Health appointment system.

Time frame: 3 months

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Fact Sheet ArmRate of Genetic Counseling and Testing Uptake.Counseling18 Participants
Fact Sheet ArmRate of Genetic Counseling and Testing Uptake.Testing7 Participants
YouTube Video ArmRate of Genetic Counseling and Testing Uptake.Counseling15 Participants
YouTube Video ArmRate of Genetic Counseling and Testing Uptake.Testing12 Participants
Secondary

Knowledge Scale - Genetic Counseling and Testing Knowledge .

The investigators measured general knowledge about hereditary breast and ovarian cancer. GCT knowledge was ascertained using a 13 item scale developed by Erblich et al.'s (2005). Example items included have you ever heard about genetic counseling for BRCA 1 and 2? and have yes/no or true/false options. Scores across the 13 item Knowledge scale were summed with a range of ( 0-13) where higher values indicated higher knowledge.

Time frame: Baseline was collected up to 48 hours from the start of the intervention and the follow-up was assessed within 48 hours post-intervention.

ArmMeasureGroupValue (MEAN)Dispersion
Fact Sheet ArmKnowledge Scale - Genetic Counseling and Testing Knowledge .Follow-up7.79 score on a scaleStandard Deviation 1.9
Fact Sheet ArmKnowledge Scale - Genetic Counseling and Testing Knowledge .Baseline7.69 score on a scaleStandard Deviation 1.75
YouTube Video ArmKnowledge Scale - Genetic Counseling and Testing Knowledge .Follow-up8.11 score on a scaleStandard Deviation 1.55
YouTube Video ArmKnowledge Scale - Genetic Counseling and Testing Knowledge .Baseline7.50 score on a scaleStandard Deviation 1.45
Secondary

Self-efficacy Scale

The investigators measured participants self-efficacy in genetic counseling services.Self-efficacy was measured with 3 items on a 5-point likert-scale, with questions that was developed for this study. Example items include how confident are you that you can cope with your risk of developing cancer?. Response options are on a 5-point likert scale ranging from not at all confident (1) and very confident (5). Scores across the 3- item scale were summed with a range of (3-15) where higher scores indicated higher self efficacy.

Time frame: Baseline was collected up to 48 hours from the start of the intervention and the follow-up was assessed within 48 hours post-intervention.

ArmMeasureGroupValue (MEAN)Dispersion
Fact Sheet ArmSelf-efficacy ScaleFollow-up14.76 score on a scaleStandard Deviation 0.91
Fact Sheet ArmSelf-efficacy ScaleBaseline14.38 score on a scaleStandard Deviation 1.21
YouTube Video ArmSelf-efficacy ScaleFollow-up14.21 score on a scaleStandard Deviation 2.02
YouTube Video ArmSelf-efficacy ScaleBaseline14.29 score on a scaleStandard Deviation 2.32

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026