Improving Survivorship Among Minority Cancer Dyads

Improving Survivorship Outcomes for African American and Latinx Cancer Survivors and Caregiver Dyads Through A Culturally Based Training Program for Underserved Health Professional Students

This proposed intervention centers on improving survivorship outcomes among African American and Latinx cancer survivor and caregiver dyads. As a result, there will be four major outcomes. First, as a result of partnership with minority social institutions (e.g. faith leaders), we will develop an in-depth culturally sensitive curriculum and survivorship care plan for Cancer Survivorship and Caregiver Leaders Aimed for Minority Populations (CSC LAMPs). Second, we will increase knowledge and skills by evaluating a comprehensive cancer survivorship training program designed for underserved health professional students. Third, the implementation of this program will improve survivorship outcomes among African American and Latinx cancer survivors with advanced stage cancer and their caregivers. Lastly, this study will build sustainability for underserved minorities with the training of 30 future healthcare providers as a valuable community resource for improving cancer survivorship outcomes. The long-term outcomes of the CSC LAMPs program will generate workforce capacity and diversity in cancer-based clinical practice, research, and community advocacy for underserved minority cancer survivors and caregivers.

Study Overview

• Status: Withdrawn
• Conditions: Cancer; Breast Cancer; Lung Cancer; Colon Cancer; Caregiver Burnout
• Intervention / Treatment: Behavioral: Change in knowledge, motivation, skills, and resources

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • California
    • Los Angeles, California, United States, 90059
      • Charles R. Drew University of Medicine & Science

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Aim 1 Focus Group for Cancer Survivors and Caregivers:

Inclusion Criteria

• Individuals ages 18 and older
• identify as African American or Latinx
• identify as a cancer survivor and/or caregiver
• speak and/or understand English

Exclusion Criteria

• individuals ages 17 years or younger
• does not identify as African American or Latinx
• unable to speak or understand English
• does not identify as a cancer survivor or caregiver

Aim 1 Focus Group for Oncology Healthcare Providers:

Inclusion Criteria

• Individuals ages 18 and older
• identify as a healthcare provider
• provide care to cancer patients in current provider role
• speak and/or understand English

Exclusion Criteria

• individuals ages 17 years or younger
• unable to speak or understand English
• does not provide care to cancer patients
• does not identify as a healthcare provider

Aim 2:

Inclusion Criteria

• Individuals ages 18 and older
• registered as a CDU student
• speak and/or understand English
• considered to be underserved, which include a) identifying as an underrepresented minority: Asian, Pacific Islander, African American, Hispanic, and Native American/Alaskan Native and/or b) from a medically underserved population (i.e. faced economic, cultural or linguistic barriers to health care)

Exclusion Criteria

• individuals ages 17 years or younger
• not registered as a CDU student
• unable to speak or understand English
• not considered to be underserved

For Aim 3:

Inclusion Criteria

• cancer survivor with a participating caregiver
• stage III or stage IV cancer diagnosis
• breast, lung, or colorectal cancer diagnosis
• identify as African American or Latinx
• speak and/or understand English

Exclusion Criteria

• individuals ages 17 years or younger
• does not identify as African American or Latinx
• unable to speak or understand English
• does not identify as a cancer survivor
• cancer survivor does not identify a caregiver
• does not have a breast, lung, or colorectal cancer diagnosis
• not diagnosed with a stage III or stage IV cancer diagnosis

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Survivorship Management among African American and Latinx Cancer Dyads; This arm will implement a "one group pre-test and posttest" design to improve health outcomes of African American and Latinx cancer survivors and caregivers in collaboration with health professional students trained as Cancer Survivorship and Caregiver Leaders Aimed for Minority Populations (CSC LAMPs).	Behavioral: Change in knowledge, motivation, skills, and resources; Provide/enhance knowledge, modify attitudes, motivate and provide skills and resources to improve survivorship outcomes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Increase in psychosocial well-being using the Quality of Life: Short Form Health Survey and the Center for Epidemiologic Studies Depression Scale	By comparison from baseline to post-intervention, there will be a 25% increase in the psychosocial well-being among study participants.	3 months
Reduction of barriers to symptom management Using the Symptom Distress Scale survey	By comparison from baseline to post-intervention, there will be a 25% decrease in the barriers to symptom management among study participants.	3 months
3. Decrease in unmet needs Using the Barriers to Follow-Up Care Survey and Cancer Survivors Unmet Needs instrument	By comparison from baseline to post-intervention, there will be a 25% decrease in the unmet needs among study participants.	3 months
Reduction in caregiver burden using the Caregiver reaction assessment (CRA) survey	By comparison from baseline to post-intervention, there will be a 25% decrease in the caregiver burden among study participants.	3 months
5. Increase knowledge and utilization of supportive services using the Medical Outcomes Study Social Support Survey	By comparison from baseline to post-intervention, there will be a 25% increase in the knowledge and utilization of supportive services among study participants.	3 months

Collaborators and Investigators

• Sponsor: Charles Drew University of Medicine and Science
• Investigators: Principal Investigator: Sharon Cobb, Charles R. Drew University of Medicine & Science

Study record dates

Study Major Dates

• Study Start (Anticipated): July 1, 2021
• Primary Completion (Anticipated): June 30, 2024
• Study Completion (Anticipated): December 31, 2024

Study Registration Dates

• First Submitted: December 22, 2020
• First Submitted That Met QC Criteria: December 22, 2020
• First Posted (Actual): December 28, 2020

Study Record Updates

• Last Update Posted (Actual): July 26, 2022
• Last Update Submitted That Met QC Criteria: July 22, 2022
• Last Verified: July 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Behavioral Symptoms; Stress, Psychological; Caregiver Burden
• Other Study ID Numbers: CancerDyads

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No