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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05836129
Other study ID # 30-62050-3816
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date November 30, 2023

Study information

Verified date March 2024
Source Maharishi International University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 109
Est. completion date November 30, 2023
Est. primary completion date November 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 95 Years
Eligibility 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. -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Transcendental Meditation (TM) practice
See previous description
Other:
Stress reduction class (online)
See previous description

Locations

Country Name City State
Lebanon TM Home of Pure Knowledge Center Beirut

Sponsors (1)

Lead Sponsor Collaborator
Maharishi International University

Country where clinical trial is conducted

Lebanon, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline to 1 and 3-months on the Perceived Stress Scale(PSS-10) 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 = (week 12-baseline)
Primary Change from baseline to 1 and 3-months on the Connor-Davidson Resilience Scale (CDRS-10) The CDRS-10 measures how well one is equipped to bounce back after stressful events, tragedy, or trauma Change = (week 12-baseline)
Primary Change from baseline to 1 and 3-months on the Arabic Scale of Happiness (ASH-20) The ASH-20 seeks to conduct a global, subjective assessment of whether a person is happy or unhappy Change = (week 12-baseline)
Primary Change from baseline to 1 and 3-months on the New General Self-Efficacy Scale (NGSE-8) The New General Self-Efficacy Scale assesses how much people believe they can achieve their goals, despite difficulties. Change = (week 12-baseline)
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