- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05474547
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
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
- Name: Humaira Jamshed, PhD
- Phone Number: +923343068708
- Email: humaira.jamshed@sse.habib.edu.pk; humaira.jphd@gmail.com
Study Contact Backup
- Name: Jamshed Arslan, PhD
- Email: jamshed.arslan@gmail.com
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.
Sponsor
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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