Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
2021-07-01
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Peer Navigator Education in Improving Survivorship Care in African American Breast Cancer Survivors
NCT01450020
Study to Education Childhood Cancer Survivors About Survivorship Care
NCT01742481
Support Group Program in Improving Quality of Life in Underserved Urban Latina Breast Cancer Survivors
NCT02521961
Changing Health Behaviors to Manage Chronic Conditions in Community-dwelling African American Breast Cancer Survivors
NCT03575624
Intervening on Women's Health for Rural Young Breast Cancer Survivors
NCT05414812
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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).
Change in knowledge, motivation, skills, and resources
Provide/enhance knowledge, modify attitudes, motivate and provide skills and resources to improve survivorship outcomes.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Change in knowledge, motivation, skills, and resources
Provide/enhance knowledge, modify attitudes, motivate and provide skills and resources to improve survivorship outcomes.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* identify as African American or Latinx
* identify as a cancer survivor and/or caregiver
* speak and/or understand English
* Individuals ages 18 and older
* identify as a healthcare provider
* provide care to cancer patients in current provider role
* speak and/or understand English
* 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)
* 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
* 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:
* 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:
* 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:
* 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
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Charles Drew University of Medicine and Science
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sharon Cobb
Role: PRINCIPAL_INVESTIGATOR
Charles R. Drew University of Medicine & Science
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Charles R. Drew University of Medicine & Science
Los Angeles, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CancerDyads
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.