Evaluating Coaches for Older Adults Cancer Care and Health (COACH)
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Purpose
The overall goal of the COACH study is to conduct a comparative effectiveness trial to assess the effectiveness of trained, participant-designated health coaches versus traditional health education efforts on cancer screening among African American older adults. We hypothesize that members of older adults' extended families can be trained to be effective coaches who support them through the cancer control spectrum, i.e., prevention, screening, diagnosis and treatment.
| Condition | Intervention |
|---|---|
|
Colorectal Cancer Breast Cancer Cervical Cancer |
Behavioral: Coach Intervention (COACH) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Screening |
| Official Title: | Evaluating Coaches for Older Adults Cancer Care and Health |
- Completing at least one recommended cancer screenings (colorectal, breast, cervical) [ Time Frame: At baseline, mid-year, one year ] [ Designated as safety issue: No ]The primary outcome variables will be the change in the proportion completing at least one of the recommended screenings, comparing the COACH group to the PEM group, and the change in the proportion discussing at least one of the recommended screenings with their primary care provider (PCP), comparing the COACH group to the PEM group.
- Time to completion of cancer screenings, and the effect of comorbid conditions, health literacy, patient satisfaction,and health care costs on cancer screening [ Time Frame: At baseline, mid-year and one year ] [ Designated as safety issue: No ]Secondary outcome variables will include between-group changes in the time to completion of screenings, and the effect of comorbid conditions, health literacy, patient satisfaction, and health care costs on cancer screening.
| Estimated Enrollment: | 1100 |
| Study Start Date: | June 2012 |
| Estimated Study Completion Date: | August 2015 |
| Estimated Primary Completion Date: | August 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
No Intervention: 1. Information group
The participants and their coaches will be provided with educational brochures about cancer screening for colorectal, breast and cervical cancers at the completion of the baseline survey.
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Experimental: Coach group
The COACH intervention consists of the educational materials intervention, plus the addition of a trained, patient-designated coach.
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Behavioral: Coach Intervention (COACH)
Behavioral: Coach Intervention (COACH) The COACHES will receive a one-hour training session led by a senior level research staff member. The COACHES will be provided basic information about different types of cancer screenings, how to schedule and keep medical visits, and how to communicate with health care providers about cancer screening. The session will be interactive, including short DVD presentations, role plays and exercises. A DVD of the training modules will be provided to trainees, as well as brochures on cancer screening for the three cancer types, a checklist for the coach and a "Things to Remember" diary a checkup list, and a wellness calendar for the participants.
Other Name: COACH GROUP
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Hide Detailed DescriptionDetailed Description:
The overall goal of the COACH study is to conduct a comparative effectiveness trial to assess the effectiveness of trained, participant-designated health coaches versus traditional health education efforts on cancer screening among African American older adults. We hypothesize that members of older adults' extended families can be trained to be effective coaches who support them through the cancer control spectrum, i.e., prevention, screening, diagnosis and treatment.
1. Aims/objectives/research question/hypotheses: The overall goal of the COACH study is to conduct a comparative effectiveness trial to assess the effectiveness of trained, participant-designated health coaches versus traditional health education efforts on cancer screening among African American older adults. This research objective is guided by the theoretical model of the PRECEDE-PROCEED conceptual framework that has been widely adopted in health promotion. The target jurisdictions for this study are Baltimore City (BC) and Prince George's County (PGC), Maryland. The study is anchored in community-based participatory research (CBPR) principles, involving community members in all its phases. The CBPR component is guided by Community Advisory Groups (CAGs) representing key stakeholders in the two jurisdictions. The CAGs are essential in determining the questions included in data collection instruments, mechanisms of recruitment, interpretation of findings, and dissemination of results within the target communities.
This mixed methods study will occur in three phases: (Aim 1) a formative exploratory phase involving in-depth qualitative interviews that will inform Aims 2 and 3; (Aim 2) development and pilot testing of all COACH research protocols, including coach training curriculum, quantitative surveys, recruitment protocols among 50 participants and 25 coaches; and (Aim 3) a full-size randomized trial involving recruitment of total 550 study participants and 275 coaches, randomization, and longitudinal data collection.
Aim 1: Implement formative research to inform COACH intervention (IRB Number 00003825): As of June 2012, we have conducted in-depth interviews reaching saturation with twelve stakeholders; six healthcare providers and six community leaders. The interviews were transcribed and analyzed providing crucial information for the development of the research in Aims 2 and 3.
Aim 2: Development and pilot testing of all COACH protocols among 50 index participants and 25 participant-designated coaches: Using convenience sampling, we will recruit and enroll African American residents (1:1 men to women) of Baltimore City and Prince George's County who are aged 65-74 years. We will conduct a pilot study to assess the coaches' effect (versus traditional health education using an educational brochure) on overcoming the participants' barriers to discussing cancer screening with their primary care providers and, if needed, to getting screened for breast, cervical, and/or colorectal cancers.
Aim 3: Implementation of full randomized COACH trial among 550 total participants and 550 total coaches: Using convenience sampling, we will recruit and enroll African American residents (1:1 men to women) of Baltimore City and Prince George's County who are aged 65-74 years. We will utilize our study's IRB-approved flyer to recruit potential study participants in medical centers, senior housing, neighborhood development centers, markets, and community centers in various neighborhoods in our study's catchment areas. Eligible and interested participants will complete an in-person baseline interview administered by a trained interviewer. The participant will then be randomized, stratifying by county and gender, to one of the following two interventions: (1) printed educational materials only (PEM) or (2) printed educational material plus specialized training for his/her health coach to help the participant overcome his/her barriers to cancer screening (COACH). The coach will then complete a short interviewer-administered questionnaire. If the participant is randomized to COACH, then the coach will be invited to participate in a one-hour in-person, small group training. Participants and coaches will then be queried at 6-months and one year to assess their cancer screening status and other outcomes of interest.
The primary outcome variable of the COACH intervention will be the change in the proportion of participants completing at least one of the recommended screenings, comparing the COACH group to the PEM group during follow up. Another primary outcome will be the change in the proportion of participants who report talking with their healthcare provider regarding at least one of the recommended cancer screening(s) during follow up. Secondary outcome variables will include between-group changes in the time to completion of screenings, changes in cancer screening barriers, and changes in the reported levels of stress for both the participants and coaches.
Eligibility| Ages Eligible for Study: | 65 Years to 74 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Resident in Baltimore City, MD or Prince George's County, MD
- African American
- 65-74 years of age
- Enrolled in Medicare Parts A and B
- No screening for breast, cervical and/or colorectal cancers within the recommended time period
Exclusion Criteria:
- Diagnosis of colon, cervix or breast cancer within the past 5 years
- A current diagnosis of another cancer
- Enrollment in Medicare managed care
- Residence in a chronic care facility, being otherwise institutionalized
- Inability or unwillingness to give informed consent
Contacts and Locations| Contact: Jean G Ford, MD | 443-287-5181 | jford@jhsph.edu |
| Contact: Ilana S Mittman, MS, PhD | 443-287-7480 | imittman@jhsph.edu |
| United States, Maryland | |
| Johns Hopkins Center to Reduce Cancer Disparities | Recruiting |
| Baltimore, Maryland, United States, 21202 | |
| Contact: Jean G Ford, MD 443-287-5181 jford@jhsph.edu | |
| Contact: Ilana S Mittman, MS, PhD 4432877480 imittman@jhsph.edu | |
| Principal Investigator: Jean G Ford, MD | |
| Principal Investigator: | Jean G Ford, MD | Johns Hopkins Center to Reduce Cancer Disparities |
More Information
Additional Information:
Publications:
| Responsible Party: | Jean Ford, Associate Professor; Department of Epidemiology, Director of Johns Hopkins Center to Reduce Cancer Disparities; Associate Director of Community Programs and Research, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins Bloomberg School of Public Health |
| ClinicalTrials.gov Identifier: | NCT01613430 History of Changes |
| Other Study ID Numbers: | U54CA153710, U54CA153710 |
| Study First Received: | June 5, 2012 |
| Last Updated: | June 18, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
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Breast Neoplasms Uterine Cervical Neoplasms Colorectal Neoplasms Neoplasms by Site Neoplasms Breast Diseases Skin Diseases Uterine Neoplasms Genital Neoplasms, Female Urogenital Neoplasms Uterine Cervical Diseases |
Uterine Diseases Genital Diseases, Female Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Digestive System Diseases Gastrointestinal Diseases Colonic Diseases Intestinal Diseases Rectal Diseases |
ClinicalTrials.gov processed this record on May 23, 2013