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NCT Number: NCT07436078

Culturally Adapting an Intervention to Increase Genetic Testing in African American Cancer Survivors

The goal of this clinical trial is to culturally adapt an educational genetic counseling intervention to increase the uptake in genetic counseling and testing among African Americans at risk for heredity cancers. With the help of community stakeholders and clinical genetic professionals the investigators will:

* adapt and refine a culturally relevant online educational genetic counseling program for at-risk African Americans * Test the effects of the educational program * collaborate with community leaders and clinical genetic professionals to translate study findings, develop a road map for dissemination to the community, and identify barriers to prepare for future trials.

Participants from Detroit Research on Cancer Survivor group will be offered enrollment. Once consent is obtained, questionnaires will be completed before an online genetic counselling intervention immediately after, and at 3 months

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Key information

Age range

20 year–79 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Karmanos Cancer Institute

Detroit, Michigan, 48201, United States

Location status: Recruiting

Location contact

Felicity WK Harper, Ph.D

PRINCIPAL_INVESTIGATOR

Hayley Thompson, Ph.D

SUB_INVESTIGATOR

Jasminder Phalore, MPH

CONTACT

[email protected]

313-576-9735

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Participants enrolled in Detroit Research on Cancer Survivors (Detroit ROCS)
  • Diagnosis of Primary Breast, prostate, or colorectal cancer on or after 1/1/2013
  • have received or currently receiving care at Karmanos Cancer Institute
  • meet one or more of the National Comprehensive Cancer Network (NCCN) guidelines for cancer genetic testing as described below

Female breast

  • personal diagnosis at age ≤50
  • personal history of the triple-negative subtype
  • at least 1 close (first- or second-degree) relative diagnosed with breast cancer at age <50
  • at least 1 close relative diagnosed with ovarian cancer
  • 2+ close relatives diagnosed with breast or prostate cancer
  • age <50 AND another primary breast cancer at any age
  • 2+ primary breast cancers at any age

OR Prostate

  • personal history of high-risk or very high-risk prostate cancer
  • personal history of regional or metastatic prostate cancer
  • personal history of less than high-risk prostate cancer with a suggestive family history (i.e., father or brother or multiple relatives with prostate cancer diagnosed at age <60; at least 1 relative with breast, ovarian, or pancreatic cancer; or at least 1 relative with colorectal, ovarian, pancreatic, or kidney cancer)

OR Colorectal

  • personal diagnosis at age ≤50
  • at least 1 close relative diagnosed with HNPCC at age <50
  • at least 2 close relatives diagnosed with an HNPCC cancer at any age
  • colorectal and >=1 primary endometrial, ovarian, gastric, pancreatic, or prostate

Exclusion criteria

  • Previous genetic counseling and/or testing

Treatment and study plan

Culturally adapted Online Genetic Counseling and Testing Information

Behavioral

Testing the effects of the educational intervention designed to increase the uptake of genetic counseling testing among at-risk African American survivors

Primary outcomes

  1. Uptake of genetic counseling and genetic testing

    Time frame: 3 month follow Up

    One item question will ask whether participants have participated in genetic counseling and genetic testing (Yes or No)

Secondary outcomes

  1. Intention to undergo genetic counseling and testing

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 2-item measure assesses participant's intentions to undergo genetic counseling and testing (Yes or No)

  2. Sharing Your Results

    Time frame: 3 month follow up

    This author-developed 3-item measure assesses the extent to which participants shared information from (1) the video, (2) their counseling appointment, or (3) their testing results with their family. Each item is scored individually as binary (Yes or No) with yes=sharing and no=did not share.

  3. Major Experiences of Discrimination

    Time frame: 1 day prior to intervention

    This 18-item measure assesses whether participants have had 9 major experiences of discrimination (e.g., getting employment, housing, medical care) happen to them (responses: 1=once, 2=2-3 times, 3=4+ times, or 0=never happened). Responses (range 0-27) are summed into an Experiences score with higher score = greater experiences of racism. If participants who respond (1, 2, 3), for any item, they are asked to report the last time this happened (1=past week, 2=past month, 3=past year, 4=more than a year ago). These responses are averaged to create a Frequency score (range 1-4), which is multiplied by the Experiences scores to obtain a Severity score (range 9-108) with higher scores = higher severity of major experiences of discrimination experiences. The Experiences and Severity scores will be assessed as moderators of change in the primary outcomes.

  4. Everyday Experiences of Discrimination

    Time frame: 1 day prior to intervention

    This 5-item scale measure assesses experience of discrimination that participants might experience on daily basis (e.g., poor service in a restaurant, getting harassed). Responses are (1=almost everyday, 2=at least once a week, 3=a few times a month, 4=a few times a year, 5=less than once a year, 6=never). Responses (range 5-30) are summed, and all items are when reverse scored, higher scores = greater experiences of everyday discrimination. This measure will be assessed as a moderator of change in the primary outcomes.

    For item with a score of 1-4, participants are asked to name the main reason for the discrimination (examples: ancestry or national origin, gender, race, age, religion, weight). This item is described qualitatively.

  5. Interpersonal Processes of Care Survey

    Time frame: 1 day prior to intervention

    This 13-item scale is designed to measure race-specific perceptions of communication between patient and healthcare providers (e.g., compassion, discrimination, and disrespectful office space). Responses are (1=never, 2=rarely, 3=sometimes, 4=usually, 5=always). The first 9 items (mean range 1-5) with higher scores=higher levels of compassion and (reverse scored) lower discrimination. The next 4 items (mean range 1-5) with higher scores=higher disrespectful attitudes from office staff. The two subscales will be assessed as moderators of change in the primary outcomes

  6. Group-Based Medical Mistrust Scale

    Time frame: 1 day prior to intervention

    This 12-item scale was developed to measure race-based medical mistrust: the suspicion of mainstream health care systems and professionals and the treatment provided to individuals because they are African American. The items are scored with responses (1=strongly disagree, 2=disagree, 3=neither agree or disagree, 4=agree, 5=strongly agree). Higher scores (mean range 1-5)=higher levels of mistrust of providers. This measure will be assessed as a primary outcome of the intervention

  7. Perceived Access to Health Care Services

    Time frame: 1 day prior to intervention

    This 13-item, 4-point Likert-style scale was designed to measure perceptions of ability to get care, considering barriers such as cost, availability, and cultural fit. The scale includes items on cost and access to services. The responses are (1=strongly disagree., 2=disagree, 3=agree, 4=strongly agree) with a mean range of 1-4. Higher score=greater participation in cancer screening and a higher family income level.

  8. Perceived risk of carrying genetic mutation

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 1-item measure ("How likely do you think it is that you carry a genetic mutation that increases your risk for cancer?") assesses perceived risk of carrying a genetic mutation that increases risk for cancer. The item is scored (1=not at all to 5=extremely likely; range 1-5). Higher scores=higher perceived likelihood of carrying a genetic mutation.

  9. Attitudes about genetic counseling and testing

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 8-item scale is designed to measure positive and negative attitudes about the genetic counseling and testing process using the following 8 adjectives: worthwhile, worrying, reassuring, uncomfortable, wise, healthy, unpleasant, and important. Responses are (1=strongly disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, 5=strongly agree). Higher summed scores (range is 8-40)=more positive attitudes.

  10. Behavioral beliefs about genetic counseling

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 30-item scale measures genetic counseling-related beliefs and concerns across the following 6 subscales: "pros" of genetic counseling, "cons" of genetic counseling, competing concerns, cultural concerns, logistic concerns, and desire for more information. The responses are (1=strongly disagree, 2=moderately disagree, 3=neither agree nor disagree, 4=moderately agree, 5=strongly agree). Higher scores (range 15-75)=more positive beliefs.

  11. Perceived norms

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 10-item measure assesses injunctive and descriptive norms (5 items each) about genetic counseling. Responses are scored on a 5-point Likert scale (1=strongly disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, 5=strongly agree). Higher scores (range 1=25)=stronger perceived norms for each of the subscales ((injunctive norms and descriptive norms, respectively).

  12. Knowledge of Genetic Counseling

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 5-item scale is designed to evaluate an individual's basic knowledge of the genetic counseling process (e.g., How much have you read or heard about genetic counseling for: inherited disease? Cancer, in general?). Items are scored (1=very much to 7=not at all). (Reversed) Higher scores (mean range 1-7)=higher knowledge of genetic counseling.

  13. Perceived self-Efficacy

    Time frame: 1 day Pre Intervention to 1 day Post Intervention

    This 10-item measure assesses participant's perceived self-efficacy for pursuing genetic counseling if they were interested. Responses are (1=strongly disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, 5=strongly agree). Higher scores (mean range=1-5)=higher self efficacy for pursuing genetic counseling.

  14. Multidimensional Impact of Cancer Risk Assessment

    Time frame: 3 month Follow Up

    This 25-item scale is designed to evaluate participant emotional responses after genetic testing, regardless of result, across 3 subscales (Distress, Uncertainty, and Positive Experiences-reverse scored). The responses are 0=never, 1=rarely, 3=sometimes, 5=often. Total summed score range=0-95. Higher scores=stronger emotional impact of testing results on the individual. The measure will be assessed as part of the intervention outcomes.

  15. Cancer Family Impact

    Time frame: 3 Month Follow Up

    This 18-item scale is designed to measure the flow of information and communication about cancer in families, thoughts about family norms about cancer prevention, and the effects of cancer on families across 5 subscales (Flow: flow of information about cancer in families; Negative: negative effects of cancer on the family; Positive: positive effects of cancer on the family; Communicate: how families communicate with each other about cancer; and Norm: reaction to family norms about cancer prevention). The responses are (0=strongly disagree, 1=disagree, 2= neither agree or disagree, 3=agree 4= strongly agree). Higher total (range 0-90) summed scores=greater communication about cancer within the family. The measure will be assessed as part of the intervention

Other outcomes

  1. Age at enrollment (measured in years)

    Time frame: 1 day prior to intervention

    Covariate of the primary outcome

  2. PROMIS (Patient-Reported Outcomes Measurement Information System) Anxiety Scale

    Time frame: 1 day prior to intervention

    This 8-item measure of anxiety will be used as a covariate of the primary outcome. Responses are (1=never, 2=rarely, 3=sometimes, 4=often, 5=always). Higher scores (mean range (1-5)=higher anxiety.

  3. PROMIS (Patient-Reported Outcomes Measurement Information System) Depression Scale

    Time frame: 1 day prior to intervention

    This 8-item measure of depression will be used as a covariate of the primary outcome. This 8-item measure of anxiety will be used as a covariate of the primary outcome. Responses are (1=never, 2=rarely, 3=sometimes, 4=often, 5=always). Higher scores (mean range=1-5)=higher depression.

  4. Education (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Categorical assessment of education. Descriptive responses are (1=Employed full time (including self-employed); 2=Employed part time; (including self-employed); 3=Homemaker; 4=Unemployed; 5=Retired; 6=Disability; 7=Other (specify); 8=Employed; not otherwise specified)

  5. Income (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Categorical assessment of income. Descriptive responses are (1=Less than $20,000; 2=$20,000-$39,999; 3=$40,000-$59,999; 4=$60,000-$79,999; 5=$80,000 or more)

  6. Employment (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Categorical assessment of employment. Descriptive responses are (1=Employed full time (including self-employed); 2=Employed part time; (including self-employed); 3=Homemaker; 4=Unemployed; 5=Retired; 6=Disability; 7=Other (specify); 8=Employed; not otherwise specified)

  7. Health literacy (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    This 3-item measures health literacy: confidence in reading health-related literature (1=extremely confident to 5=not at all confident; higher scores=lower health literacy), having access to a computer (yes or no), and difficulty using a computer to access health-related information (yes or no), where no=health literacy issues.

  8. Cancer characteristics (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Categorical assessment of SEER summary stage at diagnosis. Responses are (1=localized, 2=regional, 3=distant); higher scores=more advanced cancer

    Categorical assessment of cancer site. Responses are (1=female breast, 0=male prostate)

  9. Comorbities (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Categorical assessment of comorbities.

    • Atrial fibrillation
    • Arthritis
    • Coronary artery disease
    • Congestive Heart Failure
    • COPD (chronic obstructive pulmonary disease)
    • Depression
    • Diabetes
    • Emphysema
    • Fracture (broken bone), over age 50
    • High cholesterol
    • Hepatitis (any type)
    • Heart Attack
    • Stroke
    • Thyroid problem

    Responses are 1=yes and 2=no: Comorbidity Count - Count of Heart Problems (MI, CHF, CAD, and AFIB), COPD/Emph, Stroke, High Blood Pressure, High Cholesterol, Hepatitis, Arthritis, Diabetes, Fracture (over 50), Thyroid, Dpression, and Obesity

  10. BMI (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    BMI category derived from height and weight 0 = Underweight;

    • = Normal Weight;
    • = Overweight;
    • = Obese
  11. Family cancer history (covariate of the primary outcome)

    Time frame: 1 day prior to intervention

    Count of number of blood relatives with cancers that meet NCCN guidelines for increased genetic risk

Study contacts

Contact information is provided by the study sponsor or research team.

Jasminder Phalore, MPH

CONTACT

[email protected]

313-576-9735

Sponsors and collaborators

Lead sponsor

Barbara Ann Karmanos Cancer Institute

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

A Community-Engaged Approach to Culturally Adapting an Intervention to Increase Uptake of Genetic Testing Among African American Cancer Survivors

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Feb 27, 2026
Registry last updated
Jun 23, 2026

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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