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Clinical Trials/NCT06468410
NCT06468410CompletedNot Applicable

The Influence of Hatha Yoga Duration on Pulmonary Function in Sedentary Youth: An Acute and Four-Week Intervention Study

Monira Aldhahi1 site in 1 country20 target enrollmentStarted: January 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
Forced Expiratory Volume in 1 second (FEV1)

Study Overview

Brief Summary

The goal of this clinical trial is to to investigate the acute and chronic effects of a four-week hatha yoga (HY) exercise program with different durations (60 min and 30 min) on pulmonary function in sedentary young individuals.. The main questions it aims to answer are:

• Does a four-week hatha yoga (HY) more effective than 30 min of a four-week hatha yoga (HY) and the control group in improving the pulmonary function? Researchers will compare a four-week OF 60 min duration hatha yoga (HY) , 30 min duration of HY and control to see the differences in the pulmonary function among high school sedentary students

Participants will:

Participants will be randomly assigned to one of three groups:

  1. 60-minute Hatha Yoga group (60mHY, n=21)
  2. 30-minute Hatha Yoga group (30mHY, n=21)
  3. Control group (CG, n=21)

Detailed Description

Objective: To investigate the acute and chronic effects of a four-week hatha yoga (HY) exercise program with different durations (60 minutes and 30 minutes) on pulmonary function in sedentary young individuals aged 15-16 years.

Study Design: Randomized Controlled Trial (RCT)

Participants:

• Sample Size: 52 sedentary individuals

Inclusion Criteria:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
15 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •High school adolescence
  • •Sedentary lifestyle (defined as not participating in regular physical activity for at least 6 months.

Exclusion Criteria

  • •Any known history of pulmonary, cardiovascular, or musculoskeletal conditions that would contraindicate exercise,
  • •participation in any other exercise program during the study period
  • •obesity (BMI > 25)
  • •Participants who are on medication that stimulates the heart of medication such as antibiotic use were excluded from the study

Arms & Interventions

60-minute Hatha Yoga group

Active Comparator

• 60mHY Group: Participants will undergo a 60-minute hatha yoga session twice a week for four weeks.

Intervention: short duration Hatha Yoga (Other)

30-minute Hatha Yoga group

Active Comparator

• 30mHY Group: Participants will undergo a 30-minute hatha yoga session twice a week for four weeks.

Intervention: long duration Hatha Yoga (Other)

Control group

Placebo Comparator

• Control Group: Participants will receive information about physical activity guidelines but will not engage in any structured yoga exercise during the study period.

Intervention: Control group (Other)

Outcomes

Primary Outcomes

Forced Expiratory Volume in 1 second (FEV1)

Time Frame: at baseline and end of 4 week

spirometry will be used to measure Forced Expiratory Volume in 1 second (FEV1). It is the volume of air (in liters) exhaled in the first second during forced exhalation after maximal inspiration.

Forced Vital Capacity (FVC)

Time Frame: at baseline and end of 4 week

the maximum amount of air a person can exhale after taking a deep breath measured using spirometry

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Monira Aldhahi
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Monira Aldhahi

Associate professor

Princess Nourah Bint Abdulrahman University

Study Sites (1)

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