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Pilot Study to Evaluate the Effect of Transcendental Meditation on Telomere Activity and Well-Being Among Nurse Managers

S

Sarasota Memorial Health Care System

Status

Invitation-only

Conditions

Meditation

Treatments

Behavioral: Transcendental Meditation

Study type

Interventional

Funder types

Other

Identifiers

NCT07165795
2288149-1

Details and patient eligibility

About

The objective of this study is to evaluate the impact of a health and coping strategy (Transcendental Meditation, or TM) on Telomere Length and Telomerase Activity (known markers of physiological and psychological stress and aging), Perceived Stress, Work Life Balance, Flourishing, Power as Knowing Participation in Change, and Burnout, among nurse managers.

Aim 1: To evaluate the effects of TM compared to usual care delayed instruction on TL and TA.

Aim 2: To evaluate the effects of TM compared to usual care delayed instruction on work life climate, flourishing, perceived stress, burnout, and power as knowing participation in change.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Nurse managers within the Sarasota Memorial Health Care System (SMHCS);
  • Stable for at least two months on any prescribed medications (for example, anti-anxiety or anti-depressant medications)

Exclusion criteria

  • prior instruction in the TM technique

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Immediate TM Instruction
Experimental group
Description:
This group will receive initial TM instruction within three weeks of baseline assessments with follow-up interventions every 2-4 weeks and an expectation of home practice of two 20min meditation sessions per day.
Treatment:
Behavioral: Transcendental Meditation
Control Group (delayed instruction)
No Intervention group
Description:
This group will be eligible to receive TM instruction upon completion of the final 4-month assessments, and asked to continue with routine activities throughout study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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