Actively Recruiting

Phase Not Applicable
All Genders
ID07291011

Mindfulness-Based Stress Reduction Program for Mental Health in Cancer Patients Living in Underserved and Rural Minnesota

Led by Mayo Clinic · Updated on 2025-12-18

30

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a virtual stress reduction program using mindfulness-based stress reduction (MBSR) techniques to improve mental health outcomes in cancer patients living in underserved or rural areas of Minnesota. These regions face a shortage of mental health care, making access difficult. The study aims to see if MBSR can help patients manage stress, reduce anxiety, and improve overall well-being by providing support from home. Participants will take part in weekly MBSR sessions for eight weeks delivered virtually. The program focuses on teaching mindfulness and relaxation techniques to help patients cope with stress related to cancer and its treatment. Additional ancillary studies such as electronic health record review and questionnaires are part of the intervention. During the study, researchers will assess how many patients complete the program and measure changes in stress, anxiety, and mindfulness at the start, after the eight-week course, and again at three and six months. They will also investigate any barriers patients face in completing the course. The total time for primary outcome measurement is up to ten weeks post-enrollment.

CONDITIONS

Brief Title

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

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a history of cancer or currently have cancer
  • Patients reporting greater than 4 out of 10 emotional distress within the past two weeks
  • Have a computer or smartphone
  • Willing to complete questionnaires
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 8 weeks

Participants take part in weekly Mindfulness-Based Stress Reduction (MBSR) sessions to support mental health.

Weekly visits for 8 weeks

Follow-up

Duration - Up to 6 months

Participants complete questionnaires to assess changes in stress, anxiety, and mindfulness up to 6 months after the MBSR course.

Visits at completion of the 8-week course, 3 months, and 6 months

Trial Site Locations

Total: 1 location

1

Mayo Clinic in Rochester

Rochester, Minnesota, United States, 55905

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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