search
Back to results

Enhance the Use of Genetic Counseling and Testing in Latinas

Primary Purpose

Hereditary Breast and Ovarian Cancer Syndrome

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Culturally-Targeted Video
FORCE Fact Sheet
Sponsored by
Georgetown University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hereditary Breast and Ovarian Cancer Syndrome focused on measuring Latinas, Intervention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Older than 18 years-old
  • Self-identify as Latina
  • Fluent in Spanish
  • Meet NCCN criteria for breast and/or ovarian genetic cancer risk assessment based on -personal or family history of cancer
  • Have not received genetic counseling or genetic testing
  • Able to provide informed consent
  • No other members of the same family have participated
  • Must have access to the internet via smartphone, computer, or another device.

Exclusion Criteria:

  • Not fluent in Spanish
  • Previously received genetic counseling or genetic testing for HBOC
  • Previously participated in another interventional study about HBOC and GCRA

Sites / Locations

  • Capital Breast Care Center
  • Nueva Vida
  • Arlington Free Clinic
  • Virginia Commonwealth University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Culturally-Targeted Video

FORCE Fact Sheet

Arm Description

Outcomes

Primary Outcome Measures

Genetic counseling uptake
Proportion of participants that receive genetic counseling. The outcome will be assessed by self-report (e.g., Have you received genetic counseling in the past three months?) and confirmed with the genetic counseling company records.

Secondary Outcome Measures

Genetic testing uptake
Proportion of participants that receive genetic testing. The outcome will be assessed by self-report (e.g., Have you received genetic testing in the past three months?) and confirmed with the genetic counseling company records.

Full Information

First Posted
June 18, 2020
Last Updated
April 25, 2022
Sponsor
Georgetown University
Collaborators
Basser Center for BRCA, Nueva Vida, Inc., Capital Breast Care Center, Virginia Commonwealth University, Arlington Free Clinic
search

1. Study Identification

Unique Protocol Identification Number
NCT04544501
Brief Title
Enhance the Use of Genetic Counseling and Testing in Latinas
Official Title
A Randomized Controlled Trial to Enhance the Use of Genetic Counseling and Testing in Latinas
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
February 24, 2020 (Actual)
Primary Completion Date
January 31, 2022 (Actual)
Study Completion Date
January 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Georgetown University
Collaborators
Basser Center for BRCA, Nueva Vida, Inc., Capital Breast Care Center, Virginia Commonwealth University, Arlington Free Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators will conduct a two-arm RCT to evaluate the preliminary effectiveness of a culturally-adapted video developed by the team vs. a FORCE fact sheet on enhancing genetic cancer risk assessment (GCRA; including genetic counseling and option for genetic testing) uptake and psychosocial outcomes among Latinas at increased risk for hereditary breast and ovarian cancer (HBOC).
Detailed Description
The investigators will conduct a two-arm RCT to evaluate the preliminary effectiveness of a culturally-adapted video developed by the team vs. FORCE fact sheet on enhancing genetic cancer risk assessment (GCRA; including genetic counseling and option for genetic testing) uptake and psychosocial outcomes among Latinas at increased risk for hereditary breast and ovarian cancer (HBOC). All participants will receive referrals to free telephone genetic counseling in Spanish to address cost, pragmatic, and language barriers. The investigators will recruit 28 Latina women at-risk of HBOC (14 randomized at each arm) at three sites with sizable Latinx populations. The sites include community clinics/health organizations and hospitals with whom we have established collaborations [Georgetown University (DC); Virginia Commonwealth University (VA)]. Results will improve efforts to translate genomic guidelines into practice and will reduce disparities by evaluating a low cost highly disseminable culturally-targeted video while gathering data on effectiveness and implementation. Aim 1. Evaluate the impact of video vs. FORCE fact sheet on GCRA and testing uptake and psychosocial outcomes. Aim 2. Assess implementation potential and needs by evaluating feasibility, acceptability, reach, and adoption of the intervention arms (video and FORCE fact sheet) and of the HBOC screening process at the community clinics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hereditary Breast and Ovarian Cancer Syndrome
Keywords
Latinas, Intervention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
28 Latina women at risk for HBOC will be randomly assigned to one arm after completing the baseline assessment. We will conduct a Hybrid Type 1 design to (1) test the effectiveness of two intervention approaches (video vs. FORCE fact sheet) in enhancing GCRA uptake and psychosocial outcomes and to (2) collect data on implementation outcomes regarding the interventions (video vs. FORCE fact sheet) and the implementation of a short screening survey to identify at-risk women. Given the hybrid design, we will also conduct focus groups with clinic staff, in which we estimate 32 staff to participate. Given their participation in the focus groups, clinic staff are also considered participants, but they are not part of the randomized trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Culturally-Targeted Video
Arm Type
Experimental
Arm Title
FORCE Fact Sheet
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Culturally-Targeted Video
Intervention Description
Culturally targeted narrative video: "Is My Cancer Hereditary? Rosa Visits a Genetic Counselor." With R03 funding (R03CA191543) we developed a culturally targeted narrative video for at-risk Latinas. A multidisciplinary team of researchers collaborated with filmmakers to develop the script and video. The script was informed by health behavior conceptual models, evidence-based risk communication strategies, and formative research (40 interviews with providers and at-risk Latinas). The script addressed identified knowledge gaps (e.g., incorrect belief that pap smears screen for ovarian cancer), facilitators (e.g., inform family cancer risk), barriers (e.g., emotional concerns), and cultural factors (e.g., respect). The 18-minute video illustrates the GCRA process with the story of Rosa, a Latina cancer survivor at increased risk of HBOC. Rosa learns about HBOC risk factors, overcomes barriers, and attends genetic counseling.
Intervention Type
Other
Intervention Name(s)
FORCE Fact Sheet
Intervention Description
A publically available Spanish-language fact sheet about HBOC and GCRA developed by FORCE.
Primary Outcome Measure Information:
Title
Genetic counseling uptake
Description
Proportion of participants that receive genetic counseling. The outcome will be assessed by self-report (e.g., Have you received genetic counseling in the past three months?) and confirmed with the genetic counseling company records.
Time Frame
Baseline survey to three months after baseline
Secondary Outcome Measure Information:
Title
Genetic testing uptake
Description
Proportion of participants that receive genetic testing. The outcome will be assessed by self-report (e.g., Have you received genetic testing in the past three months?) and confirmed with the genetic counseling company records.
Time Frame
Baseline survey to three months after baseline
Other Pre-specified Outcome Measures:
Title
Breast cancer genetics knowledge
Description
Change in knowledge about HBOC and GCRA. Knowledge will be measured using a 13-item Erblich et al., 2005 scale about genetic knowledge about breast cancer. The scale has statements to which participants respond True, False, or I don't Know. The scale is scored based on the accuracy of responses. A higher score indicates higher knowledge. Scores range from 0-13.
Time Frame
Change from baseline to two weeks after baseline and change from baseline to three months after baseline
Title
Intentions to participate in genetic counseling and genetic testing
Description
Change in intentions to participate in genetic counseling and genetic testing. A 2-item scale developed by Sussner, Jandorf, Thompson, and Valdimarsdottir, 2010 will be used to assess intentions to participate in genetic counseling and testing. Participants respond to a Likert-trype scale from 1 (Not at all) to 5 (Very) how likely it is that they will participate in genetic counseling and testing in the next three months.
Time Frame
Baseline to two weeks after baseline
Title
Beliefs and attitudes about genetic counseling and genetic testing
Description
Changes in beliefs and attitudes about genetic counseling and genetic testing. The outcome will be assessed by a 30-item scale developed by Sussner, Jandorf, Thompson et al., 2012 in which participants respond to a Likert-type scale from 1 (completely disagree) to 7 (complete agree).
Time Frame
Baseline to two weeks after baseline
Title
Anticipatory Emotions
Description
Changes in anticipatory emotions about receive genetic counseling. Assessed by participants' responses to how they feel 'right now' about the specific behavior of receiving genetic counseling and testing in the next three months. Responses are in a 7-point Likert-type form (from 1-strongly disagree to 7-strongly agree).
Time Frame
Baseline to two weeks after baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Older than 18 years-old Self-identify as Latina Fluent in Spanish Meet NCCN criteria for breast and/or ovarian genetic cancer risk assessment based on -personal or family history of cancer Have not received genetic counseling or genetic testing Able to provide informed consent No other members of the same family have participated Must have access to the internet via smartphone, computer, or another device. Exclusion Criteria: Not fluent in Spanish Previously received genetic counseling or genetic testing for HBOC Previously participated in another interventional study about HBOC and GCRA
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alejandra Hurtado de Mendoza, Ph.D
Organizational Affiliation
Georgetown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Capital Breast Care Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20003
Country
United States
Facility Name
Nueva Vida
City
Alexandria
State/Province
Virginia
ZIP/Postal Code
22314
Country
United States
Facility Name
Arlington Free Clinic
City
Arlington
State/Province
Virginia
ZIP/Postal Code
22204
Country
United States
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23284
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Enhance the Use of Genetic Counseling and Testing in Latinas

We'll reach out to this number within 24 hrs