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Lowering Stress Levels of Women in Lebanon

Effects of Transcendental Meditation on Rural Women of Lebanon

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05836129
Acronym
TML
Enrollment
109
Registered
2023-05-01
Start date
2023-05-01
Completion date
2023-11-30
Last updated
2024-03-13

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

Conditions

Happiness, Resilience, Self Efficacy, Stress

Keywords

Transcendental Meditation, Rural women in Lebanon

Brief summary

The goal of this clinical trial is to compare the experiences of women who learn the TM technique to those who do not. The main questions it aims to answer are: 1. Do women in rural Lebanon who practice the TM technique experience lower stress levels compared to those who do not. 2. Do women in rural Lebanon who practice the TM technique experience increased happiness, self-efficacy, and resilience levels compared to those who do not. Participants will: * complete baseline surveys * be divided into experimental and active-control groups * those in the experimental group will learn the TM technique, the control group will be offered an online didactic course on stress reduction * both groups will complete post-test surveys at the end of 1 and 3 months * Researchers will compare experimental and control groups to see if the intervention effects stress levels.

Detailed description

Methods: We will measure the effects of TM on 62+ women of the Chouf region of Lebanon using the following measures: Perceived Stress Scale, Connor-Davidson Resiliency Scale, New General Self-Efficacy Scale, and the Arabic Scale of Happiness. This is a randomized controlled trial with an experimental group and an active wait-list control group. Measurements will be taken at baseline (pre-test) and at 1 and 3 months post-test.

Interventions

BEHAVIORALTranscendental Meditation (TM) practice

See previous description

OTHERStress reduction class (online)

See previous description

Sponsors

Maharishi International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

The statistician will not be aware of which arm the participants are in.

Intervention model description

This is a randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 95 Years
Healthy volunteers
Yes

Inclusion criteria

Females living in the Chouf region of Lebanon between the ages of 18-95. \-

Exclusion criteria

Anyone: not female, under 18 or over 95, not in sound mental condition. \-

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline to 1 and 3-months on the Perceived Stress Scale(PSS-10)Change = (week 12-baseline)The PSS measures the degree to which situations in one's life are appraised as stressful. Possible scores range from 0=never to 4=very often
Change from baseline to 1 and 3-months on the Connor-Davidson Resilience Scale (CDRS-10)Change = (week 12-baseline)The CDRS-10 measures how well one is equipped to bounce back after stressful events, tragedy, or trauma
Change from baseline to 1 and 3-months on the Arabic Scale of Happiness (ASH-20)Change = (week 12-baseline)The ASH-20 seeks to conduct a global, subjective assessment of whether a person is happy or unhappy
Change from baseline to 1 and 3-months on the New General Self-Efficacy Scale (NGSE-8)Change = (week 12-baseline)The New General Self-Efficacy Scale assesses how much people believe they can achieve their goals, despite difficulties.

Countries

Lebanon

Outcome results

None listed

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