Recruiting

MBSR

Sponsor:

Mayo Clinic

Code:

NCT07291011

Conditions

Hematopoietic and Lymphatic System Neoplasm

Malignant Solid Neoplasm

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Interventions

Electronic Health Record Review

Mindfulness Relaxation

Questionnaire Administration

Study Details

Brief summary:

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.

Conditions

Hematopoietic and Lymphatic System Neoplasm

Malignant Solid Neoplasm

Study ID

NCT07291011

Start date

Nov 5, 2025

Status verified date

Jun, 2026

Completion date

Nov 15, 2029

Anticipated

Primary completion date

Nov 15, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

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 six months
  • Patients with a Rural-Urban Commuting Area (RUCA) code of 4 or greater
  • Have a computer or smartphone
  • Willing to complete questionnaires

Exclusion Criteria:

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

Study Design

Enrollment

45 participants

Anticipated

Intervention Model

Single group

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Supportive care (MBSR)

Patients participate in MBSR sessions weekly for 8 weeks.

Interventions

Electronic Health Record Review

Ancillary studies

Mindfulness Relaxation

Receive MBSR intervention

Questionnaire Administration

Ancillary studies

Primary outcome measure

  • Completion Rate [ Time Frame: Up to 10 weeks ]
  • Change in Stress [ Time Frame: Baseline, at course completion (week 10), 3 months, 6 months ]
  • Change in Anxiety [ Time Frame: Baseline, at course completion (week 10), 3 months, 6 months ]
  • Change in Mindfulness [ Time Frame: Baseline, at course completion (week 10), 3 months, 6 months ]
  • Barriers to completion of the course [ Time Frame: At course completion (week 10) ]

Central Contacts and Locations

Central contacts

Clinical Trials Referral Office

855-776-0015mayocliniccancerstudies@mayo.edu

Ahauve Orusa, MD, MPH

507-284-5162

Locations

Mayo Clinic in Rochester

Recruiting

Rochester, Minnesota, United States, 55905

Contacts

Clinical Trials Referral Office

855-776-0015mayocliniccancerstudies@mayo.edu

Ahauve Oruse, MD, MPH

507-284-5162

Principal Investigator:

Stacy D. D'Andre

More Information

Sponsor

Mayo Clinic

Last update posted

Jun 23, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Mayo Clinic on 2026-06-23.