A Mindfulness-Based Stress Reduction Program for Improving Mental Health Outcomes for Underserved Cancer Patients in Minnesota
NCT ID: NCT07291011
Last Updated: 2025-12-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
30 participants
INTERVENTIONAL
2025-11-05
2029-11-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Supportive care (MBSR)
Patients participate in MBSR sessions weekly for 8 weeks.
Electronic Health Record Review
Ancillary studies
Mindfulness Relaxation
Receive MBSR intervention
Questionnaire Administration
Ancillary studies
Interventions
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Electronic Health Record Review
Ancillary studies
Mindfulness Relaxation
Receive MBSR intervention
Questionnaire Administration
Ancillary studies
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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
* Life expectancy \< 12 months
* Active psychiatric disease
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Stacy D D'Andre
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic in Rochester
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Facility Contacts
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Stacy D. D'Andre
Role: primary
Other Identifiers
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NCI-2025-08924
Identifier Type: REGISTRY
Identifier Source: secondary_id
24-013451
Identifier Type: OTHER
Identifier Source: secondary_id
24-013451
Identifier Type: -
Identifier Source: org_study_id