- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06442371
Additional Effects of Quranic Listening Meditation in Combination With High Intensity Interval Training in Obese Adults
Additional Effects of Quranic Listening Meditation in Combination With High Intensity Interval Training on Cardiovascular Fitness and Mental Health in Obese Adults
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Khyber PkahtoonKhwa
-
Abbottābād, Khyber PkahtoonKhwa, Pakistan
- physiotherapy department, Jinnah international hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Obese adults (BMI ≥ 30)
- Age range: 18-45 years
- No previous experience with Quranic listening meditation since last 4 weeks.
- No contraindications for engaging in high-intensity physical activity
- Able to attend regular sessions at clinic and follow the study protocol.
- Willingness to undergo pre and post-assessments for cardiovascular fitness and mental health measures.
Exclusion Criteria:
- Individuals with a history of the medical condition being studied
- Those who are currently taking medication that may affect the study
- Participants with a history of mental health disorders
- Individuals who are pregnant or breastfeeding
- Those who have previously participated in a similar study
- Participants with a history of substance abuse or addiction
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High Intensity interval training + Quranic Listening
|
In this group, participants will receive protocol of High Intensity interval training which includes squats, jumping jacks, front kicks and rope jumps 3 days per week for 6 weeks, including warmup and cool down session along with Quranic listening meditation.
|
|
Active Comparator: High Intensity interval training
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In this group, participants will receive only High intensity interval training which includes squats, jumping jacks, front kicks and rope jumps 3 days per week for 6 weeks, including warmup and cool down periods with no Quranic listening meditation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified BORG Scale
Time Frame: 6 week
|
The Modified Borg Dyspnea Scale is numerical rating scale ranging from 0 to 10 and is used to measure dyspnea that patient report during sub-maximal exercise and is regularly administered during six-minute walk test.
Changes from the baseline will be measured
|
6 week
|
|
6 Min walk test (Distance in meters)
Time Frame: 6 week
|
Changes from the baseline, Body Mass Index can be define as statistical index utilizing an individual's height and weight to give an estimation of muscle versus fat in female and male of all ages.
It is determined by taking an individual weight in kilograms, separated by their height in meters squared, or BMI = weight (in kg)/height (in m square).
|
6 week
|
|
Peak VO2 with formula
Time Frame: 6 week
|
A generalized equation can be used to determined peak VO2 (Peak rate of oxygen consumption). The generalized equation can be used to accurately estimate mean peak VO2 from mean 6 MWD, among groups of patients with diverse diseases without the need for cardiopulmonary exercise testing. The equation is: Mean peak VO2(ml/kg/mins) = 4.948 + 0.023*Mean 6 MWD (meter) Changes From the Baseline will be measured |
6 week
|
|
Body Mas Index
Time Frame: 6 week
|
Changes from the baseline, Body Mass Index can be define as statistical index utilizing an individuals height and weight to give an estimation of muscle versus fat in female and male of all ages.
It is determined by taking an individual weight in kilograms, separated by their height in meters squared, or BMI = weight (in kg)/height (in m square).
|
6 week
|
|
Heart Rate recovery
Time Frame: 6 week
|
Heart rate recovery (HRR) is a measurement of how quickly your heart can settle back into its normal state following a workout.
It is the variation in heart rate between the time when you are exercising and when you stop.
|
6 week
|
|
Depression Anxiety and Stress Scale
Time Frame: 6 week
|
Depression Anxiety and Stress Scale DASS (-42), The 42-item DASS-42 self-report scale was designed to measure the negative emotional states of stress, anxiety, and depression.
As part of the larger process of clinical assessment, the DASS's main value in a clinical environment is to identify the location of emotional disturbance.
The DASS's primary purpose is to evaluate the severity of the main symptoms of stress, anxiety, and depression.
|
6 week
|
|
Systolic and diastolic blood pressure
Time Frame: 6 week
|
Changes from the Baseline, Systolic Blood pressure (SBP) and Diastolic Blood Pressure (DBP) will be measured through sphygmomanometer
|
6 week
|
|
Change in blood lipid profile
Time Frame: 6 week
|
Change in plasma total cholesterol, high density lipoproteins cholesterol (HDL), and low density lipoproteins cholesterol (LDL) after each treatment.
|
6 week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Iqbal Tariq, PhD*, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Rec/01809 Warda Zaman
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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