- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04544241
Cancer Leadership Training for Clergy Wives and Widows
March 12, 2024 updated by: Charles Drew University of Medicine and Science
Cancer Survivorship and Caregiver Leadership Education for Clergy Wives and Widows
Multiple cancer health disparities exist for underrepresented minority groups, such as higher late stage diagnoses and greater cancer-related deaths.
Among African Americans, there is an increased cancer survivorship and caregiving burden, which necessitates more support and resources during these phases.
The African American church has been evidenced to be a trusted source of resource and provide culturally competent care and contribute to decreasing these disparities.
Importantly, the leadership of the African American churches are pivotal to the health and wellness of this population.
One important leader is the clergy wife or widow, who is understudied but vital to the function of the church function and activities.
The long-term goal of this proposed study is to develop a leadership training program for clergy wives and widows with emphasis on cancer survivorship and caregiving.
The objective of this pilot project is to develop and test the Cancer Survivorship and Caregiver Leadership Education for Clergy Wives and Widows, with specific emphasis of cultural and spiritual considerations of African American cancer survivors and caregivers.
The rationale for this project, is that African American clergy wives and widows can receive the necessary training to assist cancer survivors and caregivers in the management of physical, emotional, psychosocial, spiritual, and financial challenges.
This study will be accomplished in four aims, which are 1) Develop skills and knowledge to perform an in-depth culturally sensitive need assessment and intervention map tailored for aging African American cancer survivors and caregivers, 2) To increase cancer survivorship and caregiving leadership education and activities for African American Clergy Wives and Widows, and 3) Enhance awareness of cancer-related health issues and its relationship to key determinants among aging cancer survivors and caregivers.
This project is innovative in establishing a culturally and spiritually tailored intervention to develop the training of Clergy Wives and Widows to provide appropriate education for community dwelling African American survivors and caregivers.
This research is significant because of its potential to inform cancer and caregiving related research and evidence-based practice for both health care professionals and community organizations and institutions to improve long term-health outcomes.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
37
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Los Angeles, California, United States, 90059
- Charles R. Drew University of Medicine & Science
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Identify as either a clergy wife or widow
- Identify as African American and/or Black
- Live within the boundaries of Los Angeles County
- Be at least 18 years of age
- Speak and/or read English
Exclusion Criteria:
- Does not identify as a clergy wife or widow
- Does not self-identify as African American and/or Black
- Lives outside the boundaries of Los Angeles County
- Under the age of 18
- Unable to speak and/or read English
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Clergy Wives and Widows
We will provide cancer survivorship and caregiving leadership education and activities for African American Clergy Wives and Widows by creating an educational partnership program aimed towards church-based health education on cancer survivorship and caregiving
|
We will meet with Clergy Wives and Widows monthly for 2-3 hours over 10 months.
These sessions will be delivered using innovative online format through Zoom over the ten months.
During each meeting session, experienced community and academic leaders will present their expertise with relationship to cancer survivorship and caregiving.
These individuals will have extensive experience in the particular area they are presenting in.
In addition, allotted time will be given for discussion and group activities that can be performed virtually.
To receive credit for completion of the training program, each participant must complete the training and deliver a group workshop.
All clergy wives and widows will complete a demographic questionnaire, in addition to pre- and post- intervention questionnaires
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Percentage of Participants Achieving Target Levels in Cancer Knowledge Using the Cancer Awareness Measurement Survey
Time Frame: 10 months
|
By comparison from baseline to post-intervention, there will be a 30% increase in the cancer awareness, risk factors, and screening among study participants.
|
10 months
|
Percentage of Participants Achieving Improvement in Mental Status and Wellness Using Depression, Anxiety, and Stress Survey
Time Frame: 10 months
|
By comparison from baseline to post-intervention, there will be a 30% increase in the awareness of depression, anxiety and stress among study participants.
|
10 months
|
Percentage of Participants Achieving Decreased Perceived Stigma Levels Using Cancer Stigma Scale
Time Frame: 10 months
|
By comparison from baseline to post-intervention, there will be a 30% decrease in cancer stigma among study participants.
|
10 months
|
Percentage of Participants Achieving Decreased Perceived Stress Using Caregiver Self-Assessment Questionnaire
Time Frame: 10 months
|
By comparison from baseline to post-intervention, there will be a 30% decrease in perceived stress regarding cancer caregiving among study participants.
|
10 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sharon Cobb, PhD, Charles R. Drew University of Medicine & Science
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 10, 2020
Primary Completion (Actual)
October 1, 2022
Study Completion (Actual)
October 10, 2022
Study Registration Dates
First Submitted
August 31, 2020
First Submitted That Met QC Criteria
September 3, 2020
First Posted (Actual)
September 10, 2020
Study Record Updates
Last Update Posted (Actual)
March 15, 2024
Last Update Submitted That Met QC Criteria
March 12, 2024
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1530494-1
- 5U54MD007598-15 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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