ClinicalTrials.gg
RecruitingNCT07680712Updated Nov 6, 2026

Yoga vs. Stretching-Strengthening: Physical Fitness in Sedentary Young Adults

An interventional study of yoga group and stretching-strengthening group in Sedentary Lifestlye and Exercise, sponsored by Istanbul University - Cerrahpasa. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.

Primary conditionMotor Activity(the registry's first term)UnverifiedIs this wrong?Motor Activity is a broad heading, used only when no more specific condition is named. No better condition is named, so the registry's term is kept.

Sponsored by Istanbul University - Cerrahpasa · Not applicable, Interventional, and Other

Updated Nov 6, 2026Now RecruitingSite recruiting status changed+3 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

The goal of this clinical trial is to learn if yoga or stretching-strengthening exercises are more effective in sedentary young adults who are currently healthy but at risk due to inactivity. The main questions it aims to answer are:

Which exercise type leads to better improvements in physical fitness, mental well-being, and sleep quality based on a person's starting profile?

How do initial levels of balance and muscle strength affect how well a person responds to these exercises?

Researchers will compare a yoga group to a stretching-strengthening exercise group to see if one approach is more effective than the other for specific types of individuals.

Participants will:

Be evaluated for their starting physical fitness (balance and strength) and psychological health.

Perform either yoga or stretching-strengthening exercises regularly during the study period.

Complete surveys about their mood, stress levels, and sleep quality.

Be re-tested at the end of the program to measure changes and improvements.

Read the detailed description

Sedentary lifestyle has become increasingly prevalent among young adults, leading to decreased physical fitness levels and negatively affecting psychological well-being. Although exercise-based interventions are widely recognized as effective strategies to mitigate these risks, there is limited comparative evidence regarding the differential effects of distinct exercise paradigms in healthy sedentary young individuals.

Yoga, as a mind-body intervention, integrates physical postures, breathing techniques, and mindfulness practices, and has been shown to improve flexibility, balance, muscular endurance, and psychological outcomes such as stress and well-being. On the other hand, traditional exercise programs focusing on stretching and strengthening target musculoskeletal functions more directly and are known to enhance muscle strength, endurance, and functional performance. However, studies directly comparing these two approaches under equivalent conditions (i.e., duration, frequency, and intensity) in a young, healthy sedentary population are scarce.

The primary aim of this randomized controlled trial is to compare the effects of a structured yoga program and a combined stretching and strengthening exercise program on physical fitness and psychological well-being in sedentary young adults. Additionally, the study aims to investigate how baseline physical and psychosocial profiles influence individual responses to these exercise interventions.

The study is designed as a two-arm, parallel-group randomized controlled trial. A total of 50 healthy sedentary individuals aged 18-30 years will be recruited and randomly assigned to either the yoga group or the stretching-strengthening exercise group. Both interventions will be conducted over a 6-week period, with sessions held twice per week, each lasting approximately 50 minutes.

The yoga intervention will consist of three main components: (1) breathing awareness and preparation, including pranayama and low-intensity mobility exercises; (2) a structured sequence of yoga postures (asanas) involving standing poses, balance poses, forward bends, backbends, and core stabilization exercises; and (3) a relaxation and mindfulness phase, including Savasana. The program will follow a progressive structure, gradually increasing intensity and complexity over the 6-week period.

The stretching-strengthening program will include core stabilization exercises, upper and lower extremity strengthening, and flexibility exercises. Exercises will target major muscle groups using body weight, resistance bands, and free weights, with progressive increases in repetitions, sets, and resistance. Each session will conclude with static and dynamic stretching exercises.

Outcome measures will be assessed at baseline and after the 6-week intervention period. Physical fitness parameters will include muscle strength (hand-held dynamometry), muscular endurance (sit-up test and plank duration), flexibility (sit-and-reach test), and dynamic balance (Y-Balance Test). Psychological outcomes will include psychological well-being and sleep quality, assessed using validated questionnaires. Additionally, participants' expectations regarding the intervention and their adherence and satisfaction levels will be evaluated.

02

Conditions studied

  • Sedentary Lifestlye
  • Exercise

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Keywords

  • physical exercise
  • physical inactivity
  • healthy lifestyle
03

In context

Motor Activity Unverified

9,798 studies on the registry are indexed under Motor Activity; 1,910 are open to participants now.

This study's planned enrollment of 50 is below the median of 60 across 8,388 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 699 studies on the registry; 213 are open to participants now.

Compared within Motor Activity, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being between 18 and 30 years of age,
  • Having a (BMI) of less than 30 kg/m²,
  • Being healthy (having no known systemic, neurological, psychological, or orthopedic diseases),
  • Not having participated in regular exercise within the last six months,
  • Having a sedentary lifestyle according to the World Health Organization (WHO) definition (not performing at least 150 minutes of moderate-intensity or 75 minutes of vigorous-intensity aerobic activity per week),
  • Agreeing not to participate regularly in any other physical activity or exercise program for the duration of the study,
  • Voluntarily participating in the study and agreeing to sign the written and verbal form in accordance with the principles of the Declaration of Helsinki.

Exclusion criteria

Exclusion Criteria:

  • Individuals with a history of injury, surgery, or pain complaints affecting the musculoskeletal system within the last six months,
  • Individuals with neurological, cardiovascular, respiratory, endocrine, psychiatric, or metabolic diseases,
  • Individuals who participate in any regular sporting activity,
  • Female participants who are pregnant or have a suspected pregnancy,
  • Individuals who state that they will not be able to participate regularly in the exercise program or will not be able to complete the study,
  • Individuals who do not provide written and verbal to participate in the study.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Yoga group

    6-week structured yoga program (50 min, 2 days/week).

    Other: yoga group

  • Experimental
    Stretching -Strengthening Group

    6-week core and extremity exercise program (50 min, 2 days/week)

    Other: stretching-strengthening group

Interventions

  • Otheryoga group

    The yoga group will participate in a structured beginner-level yoga program consisting of two 50-minute sessions per week for six weeks. All sessions will be conducted under the supervision of the researchers. Each session will comprise three primary phases: Preparation and Breath Awareness: 5 minutes Asana Flow: 40 minutes Deep Relaxation and Mindfulness: 5 minutes Throughout the intervention, the exercise intensity and difficulty level will be increased progressively.

  • Otherstretching-strengthening group

    The stretching-strengthening group will participate in a structured exercise program consisting of two 50-minute sessions per week for six weeks. The exercises will be performed under the supervision of the researchers. The program will comprise core stabilization, upper and lower extremity strengthening, and stretching phases. Throughout the intervention, the exercise intensity and difficulty level will be increased progressively; progression to the next level will occur when a participant can exceed the target number of repetitions without compromising proper form.

06

What researchers measure

Primary outcomes

  1. Muscle Strength

    Measured by Hand-Held Dynamometer (HHD) for deltoid, biceps, triceps, quadriceps, hamstring, and gluteal muscles. Highest value of 3 trials (kg/N)

    Time frame: Baseline

  2. Core Endurance by Plank Test duration

    Measured by Plank Test duration (seconds) following ACSM protocols.

    Time frame: Baseline

  3. Core Endurance by Sit-up Test

    Measured by Sit-up Test (repetitions in 1 minute) following ACSM protocols.

    Time frame: Baseline

  4. Flexibility

    Measured by the Sit and Reach test to evaluate hamstring and lower back flexibility (in centimeters).

    Time frame: Baseline

  5. Balance

    Measured by Y-Balance Test composite score (%) in anterior, posteromedial, and posterolateral directions.

    Time frame: Baseline

  6. Muscle Strength

    Measured by Hand-Held Dynamometer (HHD) for deltoid, biceps, triceps, quadriceps, hamstring, and gluteal muscles. Highest value of 3 trials (kg/N)

    Time frame: At the end of 6 weeks.

  7. Core Endurance by Plank Test duration

    Measured by Plank Test duration (seconds) following ACSM protocols.

    Time frame: At the end of 6 weeks.

  8. Core Endurance by Sit-up Test

    Measured by Sit-up Test (repetitions in 1 minute) following ACSM protocols.

    Time frame: At the end of 6 weeks.

  9. Flexibility

    Measured by the Sit and Reach test to evaluate hamstring and lower back flexibility (in centimeters).

    Time frame: At the end of 6 weeks.

  10. Balance

    Measured by Y-Balance Test composite score (%) in anterior, posteromedial, and posterolateral directions.

    Time frame: At the end of 6 weeks.

Secondary outcomes

  1. Psychological Well-being Score

    Assessed using the Psychological Well-being Scale (validated in Turkish by Akın, 2008). This is a multi-dimensional self-report scale that evaluates life satisfaction, self-acceptance, purpose in life, and personal growth. The total score is calculated based on the sum of the sub-dimension scores.

    Time frame: Baseline

  2. Sleep Quality

    Sleep quality will be evaluated using the Pittsburgh Sleep Quality Index (PSQI), a self-report scale used to assess the sleep quality of individuals over the past month. Global scores range from 0 to 21, where higher scores indicate poorer sleep quality. A total score of 5 or higher is considered indicative of poor sleep quality.

    Time frame: Baseline

  3. Psychological Well-being Score

    Assessed using the Psychological Well-being Scale (validated in Turkish by Akın, 2008). This is a multi-dimensional self-report scale that evaluates life satisfaction, self-acceptance, purpose in life, and personal growth. The total score is calculated based on the sum of the sub-dimension scores.

    Time frame: At the end of the 6-week intervention.

  4. Sleep Quality

    Sleep quality will be evaluated using the Pittsburgh Sleep Quality Index (PSQI), a self-report scale used to assess the sleep quality of individuals over the past month. Global scores range from 0 to 21, where higher scores indicate poorer sleep quality. A total score of 5 or higher is considered indicative of poor sleep quality.

    Time frame: At the end of the 6-weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Nov 6, 2026
Sites
Istanbul University- Cerrahpaşa is now Recruiting
Nov 6, 2026
Start date
Jun 22, 2026→Oct 19, 2026 (actual)
Nov 6, 2026
Primary completion
Mar 2027→Apr 2027
Nov 6, 2026
Study completion
Mar 2027→Apr 2027
Nov 6, 2026
Show all 1 update
  1. Nov 6, 2026
    Not yet recruiting→Recruiting
    Istanbul University- Cerrahpaşa is now Recruiting
    Start date Jun 22, 2026→Oct 19, 2026 (now actual)
    Primary completion Mar 2027→Apr 2027
    Study completion Mar 2027→Apr 2027
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07680712
Responsible party
Sezen Karaborklu Argut (Assistant Professor, Istanbul University - Cerrahpasa) — Principal investigator
First posted
Jul 2, 2026
Start date
Oct 19, 2026
Primary completion
Apr 2027 (estimated)
Completion
Apr 2027 (estimated)
Last update
Nov 6, 2026

Study contacts

Sezen Karaborklu Argut Assistant Professor, PhD
Contact
s.karaborkluargut@iuc.edu.tr
+90 212 866 37 00

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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