30 Participants NeededMy employer runs this trial

Mindfulness-Based Stress Reduction for Stroke

MO
BC
Overseen ByBethany Crouse, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: HealthPartners Institute
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to evaluate how mindfulness-based stress reduction (MBSR) can enhance emotional well-being and body awareness in individuals who have experienced a stroke. Participants will either begin the MBSR course immediately or after an 8-week waiting period. Ideal candidates for this trial include those who had a stroke at least six months ago, experience psychological distress, and have internet access for video sessions. As an unphased trial, this study provides an opportunity to explore innovative methods for improving emotional well-being post-stroke.

What prior data suggests that Mindfulness-Based Stress Reduction is safe for individuals with chronic stroke?

Research has shown that Mindfulness-Based Stress Reduction (MBSR) is generally safe and well-received by participants. Studies have found that people with chronic stroke who participated in MBSR had positive experiences. For instance, one study found that both MBSR and similar programs were well-liked, with many participants joining and staying in the programs, indicating they found it manageable and worthwhile.

Moreover, MBSR has been used in various settings and for conditions like anxiety and depression, without significant reports of negative effects. While individual experiences can differ, the evidence so far suggests that MBSR is a safe option for those considering a trial that includes this approach.12345

Why are researchers excited about this trial?

Researchers are excited about Mindfulness-Based Stress Reduction (MBSR) for stroke recovery because it offers a holistic approach that differs from traditional medical treatments like medication and physical therapy. Unlike conventional methods that primarily address physical symptoms, MBSR focuses on reducing stress through mental practices such as meditation and mindful breathing. This approach aims to enhance mental well-being and potentially improve recovery outcomes by fostering a positive mental state, which is often overlooked in standard care. Plus, MBSR is non-invasive and can be easily integrated into a patient's daily routine, making it an accessible option for many individuals.

What evidence suggests that Mindfulness-Based Stress Reduction is effective for stroke?

Research has shown that Mindfulness-Based Stress Reduction (MBSR) can greatly aid stroke recovery. In this trial, participants will either begin the MBSR course immediately or after an 8-week waitlist period. Studies have found that MBSR can reduce depression in stroke survivors, with one study noting significant mood improvement. MBSR also enhances thinking and memory skills, which are crucial after a stroke. Additionally, MBSR supports emotional well-being and overall health, making it a valuable part of recovery for many. Overall, MBSR offers promising benefits for those facing post-stroke challenges.12678

Who Is on the Research Team?

AH

Amanda Herrmann, PhD

Principal Investigator

HealthPartners Institute

Are You a Good Fit for This Trial?

Inclusion Criteria

* 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
I am available for an 8-week Friday afternoon course starting mid-May or mid-July.
I am able to understand and agree to join the study.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

3 months

Treatment

Participants undergo an 8-week Mindfulness-Based Stress Reduction (MBSR) course, consisting of 8 sessions lasting 2.5 hours each and a 1-day 7-hour retreat

8 weeks
8 sessions (in-person), 1 retreat (in-person)

Follow-up

Participants are monitored for safety and effectiveness after the MBSR course

8 weeks

Delayed Start

Participants in the waitlist control group wait for 8 weeks before starting the MBSR course

8 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Mindfulness-Based Stress Reduction (MBSR)

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Immediate StartExperimental Treatment1 Intervention
Group II: Delayed Start (Waitlist Control)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

HealthPartners Institute

Lead Sponsor

Trials
196
Recruited
3,721,000+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/36347179/

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