Meditation and Youth Mental Health (Med-YMH)

February 27, 2023 updated by: Humaira Jamshed, Habib University

Effect of Meditation on the Young Mental Health - A Feasibility Pilot Quasi-experimental Study

Youth is a crucial time of life when physical and mental well-being is critical. Students are vulnerable due to academic and pandemic stresses. Meditation research has been showing effects on improved parameters of mental health (sleep quality, attention, memory, and concentration), emotional wellbeing (reduced stress and anxiety), and physiological parameters (better metabolism, circulation, immunity, etc.), which influence the life and academic performance of students. This study is designed to examine the feasibility of conducting a meditation intervention among students of a small liberal arts university in Pakistan. Future larger and longer randomized controlled clinical trials on high-risk youth may be planned at a later stage to see the impact on academic performance and career progression.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

14

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 27 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy students

Exclusion Criteria:

  • Students suffering from a serious illness
  • Students already meditating regularly

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Meditation
Meditation for 30 min 10 days
Students will meditate for 30 min every day for 10 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Meditation Practice
Time Frame: 10 days
Determinants of Meditation Practice Inventory
10 days
Sleep quality (sleep duration, deep sleep, light sleep, REM)
Time Frame: 10 days
Sleep quality as measure by the fitness watch
10 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical activity and Heart Rate
Time Frame: 10 days
Physical activity as measure by the the fitness watch
10 days
Stress and Breathing Score
Time Frame: 10 days
Stress levels as measure by the the fitness watch
10 days
Food intake and nutrient profile
Time Frame: 10 days
Dietary pattern measured through an online app
10 days

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Internet Use
Time Frame: 10 days
Generalized Problematic Internet Use Scale - GPIUS
10 days
Nomophobia Questionnaire
Time Frame: 10 days
NMPQ
10 days
Social Networking Addiction
Time Frame: 10 days
SNAS
10 days
Emotional wellbeing
Time Frame: 10 days
Mental Health Continuum - Short Form MHC-SF; Each of the 14 items on the MHC-SF can be scored between 0 and 5, which means that the total score on the scale can range from 0 to 70 points. Higher scores indicate a higher level of emotional wellbeing.
10 days
Depression Anxiety and Stress
Time Frame: 10 days
Depression, Anxiety and Stress Score (DASS-21); The total score on the scale can range from 0 to 21 points. Higher scores indicate Severe depression while lower score indicates mild anxiety.
10 days
Resilience and Resilience Coping
Time Frame: 10 days
Brief Resilience Scale (BRS) and Brief Resilience Coping Scale (BRCS); The possible score range on the BRS is from 1 (low resilience) to 5 (high resilience). The possible score range on the BRCS is from 4 (low resilience) to 20 (high resilience).
10 days
Grit
Time Frame: 10 days
Short grit scale (Grit-S). Scores can vary from 1 point (low grit) to maximally 5 points (high grit).
10 days
Loneliness
Time Frame: 10 days
UP LAS; The score can range from 25 (low) to 100 (high).
10 days
Gratitude, Resentment and Appreciation
Time Frame: 10 days
GRAT-Short Form; higher scores are better
10 days
Happiness
Time Frame: 10 days
Oxford Happiness Questionnaire; higher score is more happiness.
10 days
Empathy
Time Frame: 10 days
Empathy Quotient, This score is on a range from 0 (low level of empathy) to 80 (high level of empathy)
10 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Humaira Jamshed, PhD, Integrated Sciences and Mathematics, Dhanani School of Science and Engineering, Habib University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

July 25, 2023

Primary Completion (Anticipated)

September 30, 2023

Study Completion (Anticipated)

December 25, 2023

Study Registration Dates

First Submitted

July 23, 2022

First Submitted That Met QC Criteria

July 23, 2022

First Posted (Actual)

July 26, 2022

Study Record Updates

Last Update Posted (Estimate)

February 28, 2023

Last Update Submitted That Met QC Criteria

February 27, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • HabibU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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