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Meditation and Emotional Intelligence

Meditation and Emotional Intelligence: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03097510
Enrollment
96
Registered
2017-03-31
Start date
2009-10-31
Completion date
2011-03-31
Last updated
2017-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Job Stress, Perceived Stress

Keywords

Perceived stress, Leadership, Transcendental Meditation

Brief summary

This randomized controlled trial evaluated the impact of the Transcendental Meditation program on emotional intelligence and perceived stress in supervisors and administrative staff in a public school system

Detailed description

The objective of this study was to determine whether a mind-body technique, known as the practice of Transcendental Meditation® (TM), could significantly increase emotional intelligence and decrease perceived stress in supervisors and administrative staff in a public school system. For this purpose, 96 participants from the administrative offices of the San Francisco Unified School District were randomly assigned to either immediate start of the TM program or to a delayed start wait-list control group. Subjects learning TM were instructed to meditate for 20 minutes twice a day for the four month duration of the project. All subjects were administered the BarOn Emotional Quotient Inventory (EQ-i) and Perceived Stress Scale (PSS) at baseline and posttest. If successful, these findings would suggest that TM could be used as a professional development program in organizations to increase emotional intelligence and decrease perceived stress, in turn enhancing leadership capacity and organizational effectiveness.

Interventions

The TM technique was taught as a standard 7 step course over 4 consecutive days. Thereafter, subjects attended bimonthly group meetings for more advanced knowledge over the four month intervention period.

Sponsors

Center for Wellness and Achievement in Education
CollaboratorUNKNOWN
Maharishi International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

data collectors and investigators were blind to treatment status of the subject

Intervention model description

randomized controlled trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* 18 years or older, * an employee of the San Francisco Unified School District (SFUSD), * attendance at an informational meeting on the TM program, * willingness to be randomly assigned to either active treatment or the control group.

Exclusion criteria

* having already learned the TM program, * not being available to attend treatment or testing sessions.

Design outcomes

Primary

MeasureTime frameDescription
Emotional Quotient Inventory (EQ-i)Change from baseline EQ-i at four monthsThe EQ-i is a self-report instrument that measures a range of non-cognitive capabilities, competencies, and skills that influence one's ability to succeed in coping with environmental demands and pressures.

Secondary

MeasureTime frameDescription
Perceived Stress Scale (PSS)Change from baseline PSS at four monthsThe PSS is a 14-item instrument that measures the degree to which situations in one's life are appraised as stressful.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026