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A Mindfulness-Based Stress Reduction Program for Improving Mental Health Outcomes for Underserved Cancer Patients in Minnesota

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Mayo Clinic

Status

Enrolling

Conditions

Hematopoietic and Lymphatic System Neoplasm
Malignant Solid Neoplasm

Treatments

Other: Questionnaire Administration
Other: Electronic Health Record Review
Behavioral: Mindfulness Relaxation

Study type

Interventional

Funder types

Other

Identifiers

NCT07291011
24-013451 (Other Identifier)
NCI-2025-08924 (Registry Identifier)

Details and patient eligibility

About

This clinical trial evaluates whether a virtual stress reduction program that uses mindfulness-based stress reduction (MBSR) techniques works to improve mental health outcomes in cancer patients living in underserved/rural regions of Minnesota. 80% of Minnesota counties are considered mental health care shortage areas. This shortage disproportionately impacts Minnesotans living in underserved and rural regions as they have to travel further for mental health care services. Interventions that provide patients with mental health resources from the comfort of their own home help to reduce barriers that limit access to mental health care. MBSR courses can help patients control their responses to stressful events, reduce the impact of chronic stress, develop more effective ways to cope with medical/psychological conditions, and increase overall sense of well-being. MBSR courses may serve as a way to bridge the gap between mental health care and patients with cancer living in underserved/rural regions of Minnesota.

Enrollment

30 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a history of cancer, or currently have cancer
  • Patients reporting > 4/10 emotional distress on a 0-10 scale within the past two weeks
  • Have a computer or smartphone
  • Willing to complete questionnaires

Exclusion criteria

  • Non-English-speaking patients
  • Life expectancy < 12 months
  • Active psychiatric disease

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Supportive care (MBSR)
Experimental group
Description:
Patients participate in MBSR sessions weekly for 8 weeks.
Treatment:
Behavioral: Mindfulness Relaxation
Other: Electronic Health Record Review
Other: Questionnaire Administration

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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