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Inner Engineering Yoga for Stress and Well-Being (ISHA-Impact Trial)

N/A
Waitlist Available
Research Sponsored by Beth Israel Deaconess Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the investigators collect these scores at the 6 pre-specified time points; i.e., at the time of consent; after completing the ieo modules but before conference; post conference completion; at 6 weeks; at 6 months and at 12 months.
Awards & highlights
No Placebo-Only Group

Summary

This trial is for the Inner Engineering In-Person Completion Course, which is offered in various locations. The study has been active since 2019 and can include up to 5,000 participants.

Who is the study for?
This trial is for individuals in the United States, over 18 years old, who have registered for the Inner Engineering Online and Completion Courses. They must be able to read and understand English but do not need any specific medical diagnosis to join.
What is being tested?
The study tests the effects of a program called Inner Engineering on various health aspects like pain, stress, sleep quality, emotions, anxiety, depression and substance use habits. Participants attend an in-person course and complete pre-modules as part of the intervention.
What are the potential side effects?
Since this trial involves a non-medical intervention focusing on yoga and meditation practices rather than drugs or medical procedures, it does not list typical side effects. However, participants may experience changes in mood or physical discomfort associated with new exercises.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the investigators collect these scores at the 6 pre-specified time points; i.e., at the time of consent; after completing the ieo modules but before conference; post conference completion; at 6 weeks; at 6 months and at 12 months.
This trial's timeline: 3 weeks for screening, Varies for treatment, and the investigators collect these scores at the 6 pre-specified time points; i.e., at the time of consent; after completing the ieo modules but before conference; post conference completion; at 6 weeks; at 6 months and at 12 months. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Changes in Perceived Stress Levels
Mood Changes
Other study objectives
Alcohol Consumption
Anxiety
Depression
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Inner Engineering InterventionExperimental Treatment1 Intervention
The intervention investigators propose for the study includes an Online Course with 7 modules, or a 10 hours long course, and a 1-2 day In-Person Course, in which participants will learn a simple 21 minute practice called Shambhavi Mahamudra Kriya, also known as Shambhavi Kriya.

Find a Location

Who is running the clinical trial?

Beth Israel Deaconess Medical CenterLead Sponsor
854 Previous Clinical Trials
12,925,951 Total Patients Enrolled

Media Library

Inner Engineering Intervention Clinical Trial Eligibility Overview. Trial Name: NCT04189146 — N/A
Nicotine Research Study Groups: Inner Engineering Intervention
Nicotine Clinical Trial 2023: Inner Engineering Intervention Highlights & Side Effects. Trial Name: NCT04189146 — N/A
Inner Engineering Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT04189146 — N/A
~750 spots leftby Nov 2025