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Yoga for Adolescents

The Effect of High Density Hatha Yoga Training on Physical Fitness, Respiratory Functions and Quality of Life in Healthy Adolescents

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04658563
Enrollment
28
Registered
2020-12-08
Start date
2020-10-01
Completion date
2020-12-01
Last updated
2021-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Yoga

Keywords

Yoga, physical fitness, adolescent, quality of life, sleep quality

Brief summary

Purpose: Specific effects of high-density Hatha Yoga(HY) training in adolescents have not yet been clarified. Aim of our study is to investigate the effects of high-density HY education on physical fitness, pulmonary function and quality of life in healthy adolescents. Methods: 28 female adolescents will be randomly divided into two groups as yoga training and control groups. Training group will receive high-density HY training for 8 weeks, two days a week under the supervision of a physiotherapist and one day a week home program. Control group will not receive any exercise. Flexibility of individuals will be determined by sit-reach, back scratching, lateral flexion tests; muscular endurance by sit-ups, sit down-stand up on chair tests, balance by time up-go test; cardiorespiratory capacity by incremental shuttle walking test(ISWT) and respiratory functions by spirometry, quality of life will be determined by with the Quality of Life Scale for Children.

Interventions

OTHERHigh Density Exercise Training Program - Yoga

A total of 8 weeks will be applied in our study, each session of the high-density yoga program will be started with 10 minute pranayama (breath) exercises as it is in classical yoga as a preliminary preparation for the participation of individuals; the program will be completed by applying 10-20 minutes warming-stretching movements, 40 minutes surya namaskar (SN) sets, 20-30 minutes dynamic yoga asanas and 10 minutes savasana. Participants will be encouraged to study the perceived difficulty levels between 14 and 17 using the Borg scale during the sessions

Sponsors

Baskent University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

\- Female adolescents between the ages of 14 and 18

Exclusion criteria

\- Individuals with recent muscular skeletal, neuromuscular and chronic systemic diseases that could prevent exercise

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Health-Related Physical Fitness - Upper extremity flexibility8 weeksLateral Flexion and Back Scratch Tests will be performed to evaluate upper extremity flexibility.
Assessment of Health-Related Physical Fitness - Lower extremity flexibility8 weeksSit and Reach Test will be performed to assess lower extremity flexibility.
Assessment of Health-Related Physical Fitness - Balance8 weeksTime up-go test will be performed to evaluate the balance levels of the patients.
Assessment of Health-Related Physical Fitness - Endurance8 weeksUpper extremity muscular endurance will be evaluated by Sit-up Test and lower extremity muscular endurance by Sit up-down on Chair Test
Cardiorespiratory endurance8 weeksIncremental Shuttle Walking Test: The test is controlled by audible warnings between two marked points, 9 meters apart; individuals will be asked to walk at increasing speed with stimulus, and each meter they walk will be recorded as a shuttle.
Assessment of Respiratory Functions8 weeksThe pulmonary functions of the individuals will be evaluated in the sitting position using the portable spirometer device (COSMED, Micro Quark Spirometer, Rome, Italy) according to the ATS/ERS criteria. The individuals who participated in the study will be informed about the test before the test. The test will be repeated twice and the best results will be recorded. The individual is seated on a chair without a cuff, a latch is attached to his nose, his mouth is asked to be closed tightly so that the edges of the mouths could fully grasp the device. In respiratory function test, forced vital capacity (FVC) (Liter-L and %), first-second forced expiratory volume (FEV1)(L and %), FEV1/FVC, peak flow rate (PEF)(L/second), 25-75% of forced expiratory flow rate (FEF (25-75%)(L)), inspiratory capacity (IC) (L) and vital capasity (VC) (L) values will be recorded along with expected values and percentages by age, height, body weight and gender.
Forced vital capacity (FVC)8 weeksForced vital capacity (FVC) will be measured in Liter and %.
First-second forced expiratory volume (FEV1)8 weeksFirst-second forced expiratory volume (FEV1) will be measured in Liter and %.
Peak flow rate (PEF)8 weeksPeak flow rate (PEF) will be measured in Liter/second.
25-75% of forced expiratory flow rate (FEF (25-75%)8 weeks25-75% of forced expiratory flow rate will be measured in Liter.
Inspiratory capacity (IC)8 weeksInspiratory capacity (IC) will be measured in Liter.
Vital capacity (VC)8 weeksVital capacity (VC) will be measured in Liter.
Assessment of quality of life8 weeksThe form which is prepared for adolescents aged 13-18 and validated and reliable in our country of The Pediatric Quality of Life Inventory. The 23 items of the scale developed for children aged 2-18 are scored between 0-100; the answers will be 100 if 'never' are preferred, 75 if 'rarely, 50 if 'sometimes, 25 if 'often, and 0 if 'always,. The higher the total score, the better the quality of life is.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026