Wellbeing, Stress Reduction and Social Cognition

Completed · Not applicable

Conditions studied: Cognitive Function 1, Social

In brief

There are many ways to improve wellbeing. This study will compare two 8-week wellbeing training programs. In addition to looking at how well the programs reduce stress and enhance wellbeing, the investigators will also ask questions about how these programs influence cognition and decision making.

Key facts

Study ID

NCT04494737

Run by

Massachusetts General Hospital

People needed

20

Starts

2021-01-05

Expected to finish

2021-08-30

Last updated by the study team

2022-08-24

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18-65 years of age.
• Right-handed.
• Able to speak, understand, and read English.
• Willing to participate in a 20-week study period and undergo 2 MRI scans at Massachusetts General Hospital (MGH).
• Able to safely undergo an MRI scan.
• Stable medication/treatment regimen (changes in medication must have occurred three months prior to enrollment in this study).
• Subjects with well-controlled vascular risk factors, such as treated hypertension, treated hyperlipidemia or well-controlled Type II diabetes (glucose levels < 250) will be included.
• Subjects with a history of cerebrovascular problems but have no persistent neurological deficits will be included.
• Available for scheduled class times for both study courses.
• Will be staying in the study area for the next 3 months.
• Able to complete up to 40 minutes of homework per day during the 8-week course.

You may not qualify if…

• Cardiovascular disease, stroke, or congestive heart failure.
• Has any of, or is; surgical aneurysm clips, neurostimulator, implanted pumps, metal fragments in eyes, pregnant, cardiac pacemaker, non-removable nitroglycerin patch, non-MRI compatible cochlear implants, any other non-MRI compatible metal in body.
• Has permanent bridgework in upper mouth that could interfere with MRI scan.
• Active hematological, renal, pulmonary, endocrine or hepatic disorders.
• A history of neurological disease or injury, including a history of seizures or significant head trauma (i.e., extended loss of consciousness, bleeding in the brain, Parkinson's disease, stroke).
• Received treatment for cancer within the last year (skin cancer will be allowed as will any cancer more than 2 years since the last treatment).
• Diagnosis of schizophrenia, post traumatic stress disorder (PTSD), bipolar disorder, or psychotic disorder at any point during lifetime.
• Diagnosis of any axis I psychiatric disorder within the last 12 months.
• Weighs more than 350 pounds
• Neurological or medical conditions that would interfere with study procedures or confound results, such as conditions that alter cerebral blood flow or metabolism.
• Unstable medications or on medications with CNS effects including cholinesterase inhibitors, memantine and antidepressants.
• Use of psychotropic medications within 12 months prior to study.
• Daily use of any medication that alters neural metabolism or blood flow, including chronic use of benzodiazepines, potent central nervous system (CNS) penetrant anticholinergic medications (for bladder control or allergies). These medications taken on an as needed basis (prn) will be allowed. (Over the counter supplements, such as Gingko and fish oil will be allowed.)
• Any other medications as reviewed by a clinician on a case-by-case basis.
• Current regular formal practice of meditation, tai chi, Feldenkrais or other mind-body practice with a teacher for more than 2 months within the past year, or more than 1 year of practice within the last 10 years. Significant prior mind-body experience as determined by the PI based on frequency, duration, recency and type of practice.
• Has claustrophobia.
• Any other criteria that will interfere with the subject's participation as determined by a study doctor.

Where it is running

• MGH — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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