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NCT07491861

Mindfulness-Based Stress Reduction for Emotional Recovery After Stroke

Active, Not Recruiting
NAAges 18+Interventional
HealthPartners Institute
~28 participants
Updated 2026-06-16 on ClinicalTrials.gov
What's tested:Mindfulness-Based Stress Reduction (MBSR)

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Assessment of MBSR Intervention Feasibility by measuring class attendance
Measured over From pre-intervention visit to the end of treatment (~8 weeks)
+3 more outcomes measured

Conditions

Chronic Stroke Patients

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Stroke

NCT07491861

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • HealthPartners Neuroscience Center

    Saint Paul, Minnesotano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Amanda Herrmann, PhD · PRINCIPAL_INVESTIGATOR · HealthPartners Institute

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Ability to consent to study participation
Age 18+
Diagnosis of stroke ≥6 months prior to enrollment
A score of 5 or more on the Kessler Psychological Distress Scale (K6)
Reliable and consistent internet access and a device with video conferencing (e.g. Zoom) capabilities (e.g., smart phone, tablet, or laptop/computer) for the duration of the study
Able to attend an 8-week mindfulness course on Friday afternoons

Exclusion

Non-English speaking
Prior completion of an MBSR course
Active participation or past participation ≤3 months in any other interventional research study
History of any serious/uncontrolled neurological, psychiatric, or substance use disorder that would impact study participation
Any other clinically relevant finding that would pose a safety risk to the subject as determined by the investigator

What this trial measures

  • Assessment of MBSR Intervention Feasibility by measuring class attendanceFrom pre-intervention visit to the end of treatment (~8 weeks)

    Feasibility of the MBSR intervention will be assessed by measuring attendance of the sessions

  • Assessment of MBSR Intervention Feasibility through item 4 of the Client Satisfaction Questionnaire (CSQ-8)From pre-intervention visit to end of treatment (~8 weeks)

    Satisfaction with the course will be measured using item 4 of the CSQ-8, which asks whether the participant would recommend the course to others.

  • Assessment of Study Feasibility through measurement of participant recruitment3-month recruitment period

    Recruitment feasibility will be assessed by measuring the number of participants recruited within the 3-month recruitment window compared to the recruitment goals of the study.

  • Assessment of Study Feasibility through measurement of participant study completion (retention)From enrollment to end of study (approximately 16 weeks)

    Retention will be measured by assessing number of recruited participants who complete all study visits.