Pilot Study to Evaluate the Effect of Transcendental Meditation on Telomere Activity and Well-Being Among Nurse Managers
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
Typical duration for not_applicable
1 active site
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
May 18, 2025
CompletedFirst Submitted
Initial submission to the registry
June 30, 2025
CompletedFirst Posted
Study publicly available on registry
September 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2027
September 10, 2025
September 1, 2025
2 years
June 30, 2025
September 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Telomere Length
T/S ratio; processed by UCSF Blackburn Labs SOP #104D
baseline, 1-month, 4-months
Telomerase Activity
(# positive copies/10,000 input cells) ; processed by UCSF Blackburn Labs SOP #104D
baseline, 1-month, 4-months
Secondary Outcomes (5)
Work-Life Climate Scale
baseline, 1-month, 4-months
Secure Flourishing Index, SFI
baseline, 1-month, 4-months
Perceived Stress Scale-10 (PSS10)
baseline, 1-month, 4-months
Maslach Burnout Inventory Human Services Survey for Medical Personnel
baseline, 1-month, 4-months
Power as Knowing Participation in Change (PKPCT)
baseline, 1-month, 4-months
Study Arms (2)
Immediate TM Instruction
EXPERIMENTALThis 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.
Control Group (delayed instruction)
NO INTERVENTIONThis 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.
Interventions
Standard TM instruction by certified TM teachers, including 4 days of initial training (60-90 min/day), then follow-up sessions (60-90 min) every 2-4 weeks.
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- prior instruction in the TM technique
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sarasota Memorial Health Care Systemlead
- Florida Atlantic Universitycollaborator
Study Sites (1)
Sarasota Memorial Health Care System
Sarasota, Florida, 34239, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 30, 2025
First Posted
September 10, 2025
Study Start
May 18, 2025
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
May 1, 2027
Last Updated
September 10, 2025
Record last verified: 2025-09