NCT07165795

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

75
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
11mo left

Started May 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress55%
May 2025May 2027

Study Start

First participant enrolled

May 18, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 30, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 10, 2025

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Last Updated

September 10, 2025

Status Verified

September 1, 2025

Enrollment Period

2 years

First QC Date

June 30, 2025

Last Update Submit

September 2, 2025

Conditions

Keywords

nurse managerwell-beingtelomeremeditation

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

EXPERIMENTAL

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.

Behavioral: Transcendental Meditation

Control Group (delayed instruction)

NO INTERVENTION

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.

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.

Immediate TM Instruction

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Sarasota Memorial Health Care System

Sarasota, Florida, 34239, United States

Location

MeSH Terms

Interventions

Meditation

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual TherapiesRelaxation TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This study is a two-group randomized clinical trial (intervention and control groups) pilot study consisting of 30 nurse managers, with 15 nursing managers randomly assigned to each group.
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

Locations