NCT03097510

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

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
96

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2009

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2009

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2011

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2011

Completed
6.1 years until next milestone

First Submitted

Initial submission to the registry

March 21, 2017

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 31, 2017

Completed
Last Updated

March 31, 2017

Status Verified

March 1, 2017

Enrollment Period

1.3 years

First QC Date

March 21, 2017

Last Update Submit

March 30, 2017

Conditions

Keywords

Perceived stressLeadershipTranscendental Meditation

Outcome Measures

Primary Outcomes (1)

  • Emotional Quotient Inventory (EQ-i)

    The 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.

    Change from baseline EQ-i at four months

Secondary Outcomes (1)

  • Perceived Stress Scale (PSS)

    Change from baseline PSS at four months

Study Arms (2)

Transcendental Meditation

EXPERIMENTAL

The TM technique is a simple, natural, effortless technique that allows the mind to experience finer levels of the thinking process until the mind transcends and experiences the source of thought, a state of deep, integrated relaxation. During the meditation session, the active mind settles down to a silent yet fully awake state of awareness. TM was taught to study participants by certified instructors, using standardized procedures for teaching.

Behavioral: Transcendental meditation

Wait list control

NO INTERVENTION

This wait list group served as the control group. After the study was completed, the wait-list controls were given the option to learn the TM technique as their reward for participating as controls during the 4 month study.

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.

Also known as: TM technique
Transcendental Meditation

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Occupational Stress

Interventions

Meditation

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual TherapiesRelaxation TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Laurent D Valosek

    Center for Wellness and Achievement in Education

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
data collectors and investigators were blind to treatment status of the subject
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Director

Study Record Dates

First Submitted

March 21, 2017

First Posted

March 31, 2017

Study Start

October 1, 2009

Primary Completion

January 1, 2011

Study Completion

March 1, 2011

Last Updated

March 31, 2017

Record last verified: 2017-03