Mindfulness program for Latino cancer patients and their caregivers
Cultural Adaptation of a Mindfulness-Based Intervention for Latino Cancer Patients and Their Caregivers
This study is testing a mindfulness program to see if it can help Latino cancer patients and their caregivers feel less stressed and improve their overall well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT04870788 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to develop and evaluate a culturally adapted mindfulness-based intervention designed to improve psychological well-being in Latino patients with advanced cancer and their family caregivers. The study involves randomizing participants into different groups to participate in mindfulness sessions either together or separately over four weeks. The primary focus is on enhancing awareness of thoughts, emotions, and sensations to alleviate stress and anxiety related to cancer. The feasibility of the intervention and its effects on psychological distress, quality of life, and cancer symptoms will also be assessed compared to a waitlist control group.
Who should consider this trial
Good fit: Ideal candidates include Hispanic/Latino individuals diagnosed with stage III-IV solid tumors who are currently undergoing active treatment and have a family caregiver willing to participate.
Not a fit: Patients who do not self-identify as Hispanic/Latino or those with earlier-stage cancers may not receive benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the mental well-being and quality of life for Latino cancer patients and their caregivers.
How similar studies have performed: Other studies have shown promise in using mindfulness-based interventions for cancer patients, suggesting potential success for this culturally tailored approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosed with a stage III-IV solid tumor * On active treatment * Self-identify as Hispanic/Latino * ECOG (Eastern Cooperative Oncology Group) performance status of =\< 2 * Willing to participate in the study with a family caregiver (e.g., spouse, adult child) with whom they currently reside and who consents to participate Exclusion Criteria: * At least 18 years old * Able to speak English or Spanish * Have access to the internet * Able to provide informed consent
Where this trial is running
Houston, Texas
- M D Anderson Cancer Center — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Larkin Strong — M.D. Anderson Cancer Center
- Study coordinator: Larkin Strong
- Email: llstrong@mdanderson.org
- Phone: (713) 563-8930
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.