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Mindfulness-Based Stress Reduction to Improve Well-being in Black Adult Cancer Survivors, Community Faith-based Mindfulness Ministry

Effectiveness of Mindfulness-Based Intervention on Patient Reported Outcomes of Black Adult Cancer Survivors: A Community Faith-Based Mindfulness Ministry (ComFaMM) Trial

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06767475
Acronym
ComFaMM
Enrollment
65
Registered
2025-01-10
Start date
2024-12-31
Completion date
2028-12-31
Last updated
2026-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm

Brief summary

This clinical trial evaluates the impact of a Mindfulness-Based Stress Reduction (MBSR) program adjusted to include Christian principles on well-being in Black adult cancer survivors. Cancer survivors face a unique set of challenges that includes not only physical but also mental and spiritual well-being. Concerns related to both diagnosis and treatment profoundly impact the quality of life of Black cancer survivors. Mindfulness-based interventions (MBIs) have been shown to be effective in improving psychological resilience, reducing anxiety, and enhancing the quality of life among cancer survivors. However, there is little research focusing on these interventions among Black adult cancer survivors. Research has shown that interventions that include cultural experiences, such as the role of religion, spirituality and faith, are more effective in maintaining psychological well-being in Black men. A MBSR program adjusted to include Christian principles may improve the well-being in Black adult cancer survivors.

Detailed description

PRIMARY OBJECTIVES: I. Develop a culturally adapted Mindfulness-Based Stress Reduction (MBSR) intervention. (Phase 0) II. Pilot test the MBSR intervention to assess its feasibility, acceptability, and preliminary efficacy among a small group of participants. (Phase 0) III. To implement an overnight silent mindfulness retreat intervention that incorporates faith based cultural adaptations tailored for Black participants. (Phase I) OUTLINE: PHASE 0: INTERVENTION DEVELOPMENT: Participants attend a focus group or a one-on-one interview over up to 60 minutes to gather insights of the cultural needs of Black adult cancer survivors. PILOT TESTING: Patients participate in a group discussion with exercises and activities on study. After completion of study intervention, patients are followed up at 3 months. PHASE 1: Patients participate an overnight silent mindfulness retreat intervention, over 31 hours, with faith-based cultural adaptation emphasizing resilience and cultural relevant spiritual framing. The retreat includes sessions on different types of meditation, working with thoughts and emotions, stress, mindfulness techniques and how to integrate them, positive mind states, resiliency and resources, including educational handouts. After completion of study intervention, patients are followed up at 3 and 6 months.

Interventions

OTHEREducational Intervention

Receive education resource handouts

OTHERDiscussion

Attend a focus group

Complete silent mindfulness retreat intervention

OTHERInterview

Attend a one-on-one interview

OTHERQuestionnaire Administration

Complete study-related questionnaires

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* PHASE 0 DEVELOPMENT: Adults aged 18 or older * PHASE 0 DEVELOPMENT: Ability to speak, read and understand English * PHASE 0 DEVELOPMENT: Individuals personally affected by cancer, either through their own diagnosis or that of a loved one * PHASE 0 DEVELOPMENT: Self-identifies as Black or African American * PHASE 0 DEVELOPMENT: Membership or affiliation with a faith-based organization * PHASE 0 PILOT TESTING: Adults aged 18 or older * PHASE 0 PILOT TESTING: History of a cancer diagnosis * PHASE 0 PILOT TESTING: Meets National Cancer Institute (NCI) cancer survivor definition (a person is a survivor from the time of diagnosis until the end of life) * PHASE 0 PILOT TESTING: Ability to physically attend live MBI and complete web-based surveys and assessments * PHASE 0 PILOT TESTING: Ability to speak, read and understand English * PHASE 1: Adults aged 18 or older * PHASE 1: History of a cancer diagnosis * PHASE 1: Meets NCI cancer survivor definition (a person is a survivor from the time of diagnosis until the end of life) * PHASE 1: Ability to physically attend live MBI and complete web-based surveys and assessments * PHASE 1: Ability to speak, read and understand English * PHASE 2: Adults aged 18 or older * PHASE 2: History of a cancer diagnosis * PHASE 2: Meets NCI Cancer Survivor definition (a person is a survivor from the time of diagnosis until the end of life) * PHASE 2: Ability to physically attend live MBI and complete web-based surveys and assessments * PHASE 2: Ability to speak, read and understand English

Exclusion criteria

* PHASE 0 DEVELOPMENT: Does not meet the inclusion criteria * PHASE 0 DEVELOPMENT: Unable or unwilling to participate in the recorded sessions * PHASE 0 PILOT TESTING: Inability to attend and participate in MBI due to medical or psychological hardship * PHASE 0 PILOT TESTING: Inability to speak, read and understand English * PHASE 1: Inability to attend and participate in MBI due to medical or psychological hardship * PHASE 1: Inability to speak, read and understand English * PHASE 1: Participated in phase 0 of the study * PHASE 2: Inability to attend and participate in MBI due to medical or psychological hardship * PHASE 2: Inability to speak, read and understand English * PHASE 2: Participated in phase 0 or phase 1 of the study

Design outcomes

Primary

MeasureTime frameDescription
Spiritual well-beingPre-MBI, Post-MBI (immediately after MBI), 3 months, 6monthsWill be measured by the change in scores on the Functional Assessment of Chronic Illness Therapy-Spiritual Well-Being Scale (FACIT-Sp-12). The FACIT-Sp-12a is a 12-item scale measuring spiritual well-being over the past 7 days. Responses are on a 5 point Likert-type scale (0=not at all; 1=a little bit, 2=somewhat; 3=quite a bit; 4=very much) with higher scores generally representing greater well-being

Secondary

MeasureTime frameDescription
Quality of life (QOL) (Phase 1)Pre-MBI, Post-MBI, 3 months, 6monthsWill be evaluated using changes in health related QOL patient reported outcomes responses. The World Health Organization Quality of Life Brief Version (WHOQOL-BREF) will be used to assess spiritual, religious or personal beliefs and how these beliefs have affected QOL including positive feelings, social support, self-esteem, pain, energy, work capacity, health and social care, and leisure activities. The WHOQOL-BREF is a 26-question instrument consisting of four domains. Each individual item of the WHOQOL-BREF is scored from 1-5 on a five-point ordinal scale.
Level of resilience - CD-RISC (Phase 1)Pre-MBI, Post-MBI, 3 months, 6monthsWill be measured by the Connor- Davidson Resilience Scale (CD-RISC). The CD-RISC is comprised of 25 items, each rated on a 5-point scale (0-4), with higher scores reflecting greater resilience.
Level of resilience - RSAPre-MBI, Post-MBI, 3 months, 6monthsWill be measured by the Resilience Scale for Adults (RSA). The RSA examines intrapersonal and interpersonal protective factors presumed to facilitate adaptation to psychosocial adversities, as well as family and social protective factors of resilience. The RSA has 33 items; item-response ranges from one to seven; higher scores reflect higher levels of protective factors of resilience.
Overall assessment of the MBI and perception of MBI value (Phase 1)Post-MBI, 3 months, 6monthsWill be assessed using the Was It Worth It (WIWI) questionnaire to determine changes in participants view on the worthiness of the intervention. Responses to the WIWI will capture participants' subjective evaluations of the intervention's impact. WIWI is a 3-item questionnaire with yes or no responses.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORFloyd B. Willis, MD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 22, 2026