Improving Survivorship Among Minority Cancer Dyads
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| 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.
|
Outcome Measures
Primary Outcome Measures
- Increase in psychosocial well-being using the Quality of Life: Short Form Health Survey and the Center for Epidemiologic Studies Depression Scale [3 months]
By comparison from baseline to post-intervention, there will be a 25% increase in the psychosocial well-being among study participants.
- Reduction of barriers to symptom management Using the Symptom Distress Scale survey [3 months]
By comparison from baseline to post-intervention, there will be a 25% decrease in the barriers to symptom management among study participants.
- 3. Decrease in unmet needs Using the Barriers to Follow-Up Care Survey and Cancer Survivors Unmet Needs instrument [3 months]
By comparison from baseline to post-intervention, there will be a 25% decrease in the unmet needs among study participants.
- Reduction in caregiver burden using the Caregiver reaction assessment (CRA) survey [3 months]
By comparison from baseline to post-intervention, there will be a 25% decrease in the caregiver burden among study participants.
- 5. Increase knowledge and utilization of supportive services using the Medical Outcomes Study Social Support Survey [3 months]
By comparison from baseline to post-intervention, there will be a 25% increase in the knowledge and utilization of supportive services among study participants.
Eligibility Criteria
Criteria
Aim 1 Focus Group for Cancer Survivors and Caregivers:
Inclusion Criteria
-
Individuals ages 18 and older
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identify as African American or Latinx
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identify as a cancer survivor and/or caregiver
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speak and/or understand English
Exclusion Criteria
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individuals ages 17 years or younger
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does not identify as African American or Latinx
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unable to speak or understand English
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does not identify as a cancer survivor or caregiver
Aim 1 Focus Group for Oncology Healthcare Providers:
Inclusion Criteria
-
Individuals ages 18 and older
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identify as a healthcare provider
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provide care to cancer patients in current provider role
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speak and/or understand English
Exclusion Criteria
-
individuals ages 17 years or younger
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unable to speak or understand English
-
does not provide care to cancer patients
-
does not identify as a healthcare provider
Aim 2:
Inclusion Criteria
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Individuals ages 18 and older
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registered as a CDU student
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speak and/or understand English
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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
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not registered as a CDU student
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unable to speak or understand English
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not considered to be underserved
For Aim 3:
Inclusion Criteria
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cancer survivor with a participating caregiver
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stage III or stage IV cancer diagnosis
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breast, lung, or colorectal cancer diagnosis
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identify as African American or Latinx
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speak and/or understand English
Exclusion Criteria
-
individuals ages 17 years or younger
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does not identify as African American or Latinx
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unable to speak or understand English
-
does not identify as a cancer survivor
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cancer survivor does not identify a caregiver
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does not have a breast, lung, or colorectal cancer diagnosis
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not diagnosed with a stage III or stage IV cancer diagnosis
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Charles R. Drew University of Medicine & Science | Los Angeles | California | United States | 90059 |
Sponsors and Collaborators
- Charles Drew University of Medicine and Science
Investigators
- Principal Investigator: Sharon Cobb, Charles R. Drew University of Medicine & Science
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CancerDyads