High Intensity Interval Training on Cardiopulmonary Parameters With or Without Facemask in Healthy Participants

Healthy Clinical Trial

Official title:

Effects of High Intensity Interval Training on Cardiopulmonary Parameters With or Without Facemask in Healthy Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05706948
• Other study ID #: REC/01370 Muneeba Fatima Tariq
• Status: Completed
• Phase: N/A
• Start date: February 15, 2023
• Est. completion date: July 1, 2023

Study information

• Verified date: July 2023
• Source: Riphah International University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To determine the effects of high intensity interval training on cardiovascular function, cardio metabolic markers and cardiorespiratory fitness in healthy individuals with or without facemask

Recruitment information / eligibility

• Status: Completed
• Enrollment: 54
• Est. completion date: July 1, 2023
• Est. primary completion date: July 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Non smoker
• Free of any heart and lung diseases
• Passed Physical Activity Readiness Questionnaire PAR-Q
• To be able to do exercise

Exclusion Criteria:

• Any physical limitation that restrict exercise
• Any neurological illness

Related Conditions & MeSH terms

• Healthy

Intervention

Other:
• High Intensity Interval Training (With Face Mask)
High Intensity Interval Training on Treadmill for 4 weeks with Face mask
• High Intensity Interval Training (Without Face Mask)
High Intensity Interval Training on Treadmill for 4 weeks with out Face mask

Locations

Country	Name	City	State
Pakistan	Islamabad Medical & Surgical Hospital	Islamabad	Fedral

Sponsors (1)

Lead Sponsor	Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pulse	Changes from the baseline, Pulse will be measured in Beats per minutes with Pulse oximeter.	4 weeks
Primary	Oxygen saturation	Changes from the baseline, Oxygen saturation will be measured in Percentages with pulse oximeter	4 weeks
Primary	Waist circumference	Waist circumference will be measured for abdominal or central fat mass. It is measured in cm at the middle distance between the last floating rib and the iliac crest using a retractable ergonomic measuring tape. Change from the baseline to 4 week will be compared	4 weeks
Primary	Modified BORG Scale	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	4 weeks
Primary	Vo2 Max	Changes from the baseline ;The maximum or optimum rate at which the heart, lungs and muscles can effectively use oxygen during exercise, used as a way of measuring a person's individual aerobic capacity.	4 weeks
Primary	Body Mas Index	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).	4 weeks
Primary	Hip circumference	Hip measurement is an estimation of the hips, utilizing a measuring tape, for assessment of spatial distance between each relating hipbone with respect to the buttocks. Hip circumference can be a significant estimation in deciding combined muscle to fat ratio around the waist that might reflect sedentary lifestyle.	4 weeks
Primary	Waist to hip ratio	Waist to hip ratio is defined as a ratio of circumference of waist to that of hip.	4 weeks
Primary	Forced Expiratory Volume in 1 second (FEV1)	Changes from the Baseline, the digital spirometer is used in clinical setting to analyze Forced Expiratory Volume in 1 second FEV1 in Liters	4 weeks
Primary	Forced vital Capacity (FVC)	Changes From the Baseline, the digital spirometer is used in clinical setting to analyze Forced vital Capacity in Liters.	4 weeks
Primary	Peak Expiratory Flow	Changes From the Baseline, the digital spirometer is used in clinical setting to analyze Peak Expiratory Flow in Liters.	4 weeks