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Muscle AchesNCT07770139

Telerehabilitation-Based Yoga Versus Yoga-Pranayama in University Students

A study testing Yoga-Pranayama and Exercise in people with Muscle Aches and Stress, run by Istanbul Gelisim University at 1 site in Turkey (Türkiye).

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

This study will compare two online exercise programs for university students: yoga alone and yoga combined with breathing exercises called pranayama. Participants will be randomly assigned to one of the two groups and will attend online sessions three times a week for four weeks. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Muscle Aches, Stress, Neck Disorders
What is being tested?
Yoga-Pranayama and Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
55 participants
Where
1 siteTurkey (Türkiye)
Study dates
Aug 2026to 30 Nov 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • University students aged 18-30 years
  • Sedentary or lightly physically active individuals
  • Ability to participate in online intervention sessions
  • Willingness to provide informed consent

Who cannot join

  • Diagnosed psychiatric disorders
  • Current use of psychotropic medications
  • Acute musculoskeletal injury
  • Advanced experience in yoga or meditation

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)1 site
  • Istanbul Gelisim University

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of Telerehabilitation-Based Yoga and Yoga-Pranayama on Stress, Anxiety, and Muscle Elastic Properties in University Students: A Randomized Controlled Trial

This study will compare two online exercise programs for university students: yoga alone and yoga combined with breathing exercises called pranayama. Participants will be randomly assigned to one of the two groups and will attend online sessions three times a week for four weeks.

The study will examine whether these programs reduce anxiety and improve the mechanical properties of the neck muscles. Muscle tone, stiffness, and elasticity will be measured using the MyotonPRO device. Anxiety and neck-related problems will also be assessed before and after the program.

The study will also investigate whether adding pranayama breathing exercises provides greater benefits than yoga alone.

Read the detailed description

The university years are a period characterized by increased stress and anxiety due to academic pressure, concerns about the future, and social transitions. These psychological burdens may negatively affect physical health by altering muscle tone and elasticity through the autonomic nervous system. While yoga improves physical flexibility and body awareness, pranayama (breath control) promotes relaxation by activating the parasympathetic nervous system. Although the individual benefits of these interventions are well established, the effects of their combination on objective physiological parameters, such as muscle elasticity, remain insufficiently investigated. Furthermore, for a population highly integrated with technology, telerehabilitation offers a critical alternative by improving accessibility and cost-effectiveness. However, evidence-based studies comparing telerehabilitation-delivered yoga interventions with combined yoga-pranayama programs are limited. Therefore, this study aims to compare the effects of telerehabilitation-based yoga and combined yoga-pranayama interventions on stress, anxiety, and muscle elastic properties in university students. The findings are expected to contribute to the physiotherapy literature by providing evidence for holistic and digitally delivered intervention models.

Participants will be randomly allocated into two groups using a simple randomization method: a yoga group and a yoga-pranayama group. The intervention will last four weeks, with sessions conducted three times per week. The yoga group will participate in 30-minute exercise sessions, whereas the yoga-pranayama group will receive 40-minute sessions consisting of 30 minutes of yoga followed by 10 minutes of pranayama.

The yoga-pranayama intervention will include yoga exercises targeting mobility and flexibility in combination with diaphragmatic breathing and alternate nostril breathing techniques. The yoga group will perform diaphragmatic breathing, thoracic expansion exercises, and postural correction exercises, including scapular retraction, chin tuck, and core activation.

Muscle mechanical properties will be assessed using a Myoton device. Stress and anxiety levels will be evaluated using the State Anxiety Inventory (STAI-I), and neck-related functional status will be assessed using the Neck Disability Index (NDI). All outcome measures will be collected before and after the intervention.

The data will be analyzed using appropriate statistical methods to determine within-group and between-group differences. This study is expected to clarify the effects of telerehabilitation-based yoga interventions on the psychological and physical health of university students and to determine the additional benefits of incorporating pranayama techniques.

Objective:

The primary objective of this study is to comparatively evaluate the effectiveness of a telerehabilitation-based yoga program and a conventional yoga-pranayama combination on psychometric outcomes (stress and anxiety) and biomechanical outcomes (muscle elasticity and mechanical properties) in university students.

Methods This study is designed as a randomized controlled trial to investigate the effects of telerehabilitation-based yoga and yoga-pranayama interventions in university students. The study population will consist of healthy young adults enrolled at a university. The sample will include volunteers who meet the predefined inclusion and exclusion criteria, and the required sample size will be determined by an a priori power analysis (α = 0.05, power = 0.80). Participants will be randomly allocated to one of two groups using a simple randomization method.

Muscle mechanical properties will be assessed using the MyotonPRO device. Anxiety levels will be evaluated using the State Anxiety Inventory (STAI-I), and neck-related functional status will be assessed using the Neck Disability Index (NDI).

Muscle mechanical properties will be measured objectively and non-invasively using the MyotonPRO device. Measurements will be performed on the upper trapezius and sternocleidomastoid (SCM) muscles in the cervical region.

During the assessments, participants will be positioned comfortably in either a supine or seated position according to a standardized protocol. Measurement sites will be identified using anatomical landmarks, and all measurements will be obtained from the same locations for each participant. For the upper trapezius muscle, the midpoint between the acromion and the spinous process of the C7 vertebra will be used as the reference point. For the sternocleidomastoid muscle, measurements will be taken from the midpoint of the muscle belly where it is most prominent.

At each measurement site, the probe of the MyotonPRO device will be positioned perpendicular to the skin surface, and a brief mechanical impulse will be applied to record the viscoelastic properties of the muscle. Participants will be instructed to remain completely relaxed during the measurements. Multiple measurements will be obtained at each site, and the average value will be used for analysis.

The recorded muscle mechanical parameters will include muscle tone (Hz), stiffness (N/m), and elasticity (logarithmic decrement). To ensure measurement reliability, all assessments will be performed by the same trained researcher under standardized environmental conditions.

All outcome assessments will be conducted by a researcher who has received standardized training in the measurement procedures. The telerehabilitation interventions will be delivered through an online platform, whereas all outcome assessments will be performed face-to-face.

The interventions will be administered three times per week for four weeks. Participants in the yoga group will complete a 30-minute exercise session, whereas those in the yoga-pranayama group will receive a 40-minute intervention consisting of 30 minutes of yoga followed by 10 minutes of pranayama.

Statistical analyses will be performed using appropriate parametric or non-parametric tests depending on data distribution. Paired statistical tests will be used for within-group comparisons, while independent-sample tests will be used for between-group comparisons. Statistical significance will be set at p < 0.05.

To minimize bias, participants will be randomly allocated to intervention groups, the outcome assessor will be blinded to group allocation, and all measurement procedures will be standardized. In addition, participants will be monitored regularly throughout the study to minimize missing data.

Sample Size The sample size was calculated using G*Power version 3.1 based on an a priori power analysis. A repeated-measures analysis of variance (ANOVA) model with a group × time interaction was used for the calculation. Based on previous studies evaluating cervical muscle viscoelastic properties using the MyotonPRO device, a moderate effect size (f = 0.30) was assumed. The significance level was set at α = 0.05, with a statistical power of 1 - β = 0.95. The analysis indicated that a minimum sample size of 44 participants was required. Considering a potential 20% dropout rate, a total of 52-56 participants will be recruited.

Inclusion Criteria

  • University students aged 18-30 years
  • Sedentary or lightly physically active individuals
  • Ability to participate in online intervention sessions
  • Willingness to provide informed consent Exclusion Criteria
  • Diagnosed psychiatric disorders
  • Current use of psychotropic medications
  • Acute musculoskeletal injury
  • Advanced experience in yoga or meditation

Literature Summary:

The literature confirms that the university years represent one of the most stressful periods in an individual's life. Academic demands and social adaptation continuously stimulate the hypothalamic-pituitary-adrenal (HPA) axis, resulting in sustained cortisol secretion. These endocrine changes trigger a protective increase in musculoskeletal tension, leading to increased muscle stiffness, reduced biomechanical elasticity, and the development of myofascial pain. Yoga and pranayama are well-established somatic interventions that regulate autonomic nervous system function. Evidence suggests that yoga enhances parasympathetic activity through vagal stimulation, while pranayama (breathing control) techniques reduce anxiety symptoms by modulating amygdala activity. At the physiological level, yoga improves tissue hydration and muscle elasticity by optimizing collagen fiber alignment through static stretching and isometric contractions.

Following the COVID-19 pandemic, digitalization in healthcare has accelerated, making telerehabilitation an important alternative because of its accessibility and cost-effectiveness. Previous studies have demonstrated that remotely supervised exercise programs can achieve clinical outcomes comparable to those of face-to-face interventions. For university students, who generally possess a high level of digital literacy, telerehabilitation represents a promising approach for improving adherence to therapeutic interventions. Although existing studies have primarily focused on the psychological benefits of yoga, its effects on objective biomechanical parameters, such as muscle elasticity, have received comparatively little attention. Furthermore, evidence comparing telerehabilitation-based yoga with combined yoga-pranayama protocols remains limited. Therefore, the present study aims to address this gap by investigating the effectiveness of digital mind-body interventions on both psychological and biomechanical outcomes.

Being tested
Yoga-Pranayama, Exercise
Keywords
students, muscle pain, stress, breathing, neck disorders
Medical subject headings
Myalgia, Respiratory Aspiration

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Yoga-PranayamaOther

    Also called Exercise, Breathing Exercise

    The interventions will be administered three times per week for four weeks. Participants in the yoga group will complete a 30-minute exercise session, whereas those in the yoga-pranayama group will receive a 40-minute intervention consisting of 30 minutes of yoga followed by 10 minutes of pranayama.

  • ExerciseOther

    Also called Yoga

    The interventions will be administered three times per week for four weeks. Participants in the yoga group will complete a 30-minute exercise session.

Study groups in NCT07770139
Study groupRoleWhat they receive
YogaActive comparatorThe interventions will be administered three times per week for four weeks. Participants in the yoga group will complete a 30-minute exercise session.
Receives: Other: Exercise
Yoga-PranayamaExperimentalThose in the yoga-pranayama group will receive a 40-minute intervention consisting of 30 minutes of yoga followed by 10 minutes of pranayama.
Receives: Other: Yoga-Pranayama

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle Tone (Hz)

    Muscle mechanical properties will be measured objectively and non-invasively using the MyotonPRO device. Measurements will be performed on the upper trapezius and sternocleidomastoid (SCM) muscles in the cervical region.

    During the assessments, participants will be positioned comfortably in either a supine or seated position according to a standardized protocol. Measurement sites will be identified using anatomical landmarks, and all measurements will be obtained from the same locations for each participant. For the upper trapezius muscle, the midpoint between the acromion and the spinous process of the C7 vertebra will be used as the reference point. For the sternocleidomastoid muscle, measurements will be taken from the midpoint of the muscle belly where it is most prominent.

    Oscillation Frequency [Hz] characterizes the intrinsic tension of biological soft tissues on the cellular level. The Oscillation Frequency of a muscle in its contracted state characterizes state of tension.

    Measured: During enrollment and after 4 week intervention.

  2. Muscle Stiffness (N/m)

    Muscle mechanical properties will be measured objectively and non-invasively using the MyotonPRO device. Measurements will be performed on the upper trapezius and sternocleidomastoid (SCM) muscles in the cervical region.

    During the assessments, participants will be positioned comfortably in either a supine or seated position according to a standardized protocol. Measurement sites will be identified using anatomical landmarks, and all measurements will be obtained from the same locations for each participant. For the upper trapezius muscle, the midpoint between the acromion and the spinous process of the C7 vertebra will be used as the reference point. For the sternocleidomastoid muscle, measurements will be taken from the midpoint of the muscle belly where it is most prominent.

    Dynamic Stiffness [N/m] characterizes the resistance of biological soft tissues to a force of deformation. The inverse of stiffness is compliance.

    Measured: During enrollment and after 4 week intervention.

  3. Muscle Elasticity (Logarithmic Decrement)

    Muscle mechanical properties will be measured objectively and non-invasively using the MyotonPRO device. Measurements will be performed on the upper trapezius and sternocleidomastoid (SCM) muscles in the cervical region.

    During the assessments, participants will be positioned comfortably in either a supine or seated position according to a standardized protocol. Measurement sites will be identified using anatomical landmarks, and all measurements will be obtained from the same locations for each participant. For the upper trapezius muscle, the midpoint between the acromion and the spinous process of the C7 vertebra will be used as the reference point. For the sternocleidomastoid muscle, measurements will be taken from the midpoint of the muscle belly where it is most prominent.

    The decrement of natural tissue oscillation serves as an inverse indicator of elastic behavior, where a higher decrement corresponds to lower elasticity. Logarithmic Decrement [relative unit]

    Measured: During enrollment and after 4 week intervention.

Secondary outcomes (3)
  1. State Trait Anxiety Inventory

    State anxiety will be assessed using the State Anxiety subscale of the State-Trait Anxiety Inventory (STAI-State). The questionnaire consists of 20 items scored on a 4-point Likert scale. Higher scores indicate greater levels of state anxiety.

    Measured: During enrollment (baseline) and after the 4-week intervention.

  2. Neck Disability

    Neck-related disability will be evaluated using the Neck Disability Index (NDI). The NDI consists of 10 items assessing pain and functional limitations in daily activities. Total scores range from 0 to 50, with higher scores indicating greater disability.

    Measured: During enrollment (baseline) and after the 4-week intervention.

  3. Chest Expansion Measurement

    Chest expansion will be assessed using a non-elastic measuring tape at the axillary, xiphoid, and subcostal levels. Measurements will be recorded during maximal inspiration and maximal expiration, and chest expansion will be calculated as the difference between inspiratory and expiratory circumferences. Greater values indicate better thoracic mobility.

    Measured: During enrollment (baseline) and after the 4-week intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Aug 2026
  2. Study startAug 2026 (estimated)
  3. Primary completion31 Oct 2026 (estimated)
  4. Study completion30 Nov 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
55 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07770139
Sponsor's protocol ID
2026-07-44
Status last verified
Jul 2026
First submitted
20 Jul 2026
Last updated
18 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Uebelacker LA, Broughton MK. Yoga for Depression and Anxiety: A Review of Published Research and Implications for Healthcare Providers. R I Med J (2013). 2016 Mar 1;99(3):20-2.

    PubMed 26929966
  • Pascoe MC, Thompson DR, Ski CF. Yoga, mindfulness-based stress reduction and stress-related physiological measures: A meta-analysis. Psychoneuroendocrinology. 2017 Dec;86:152-168. doi: 10.1016/j.psyneuen.2017.08.008. Epub 2017 Aug 30.

    PubMed 28963884
  • Gothe NP, Khan I, Hayes J, Erlenbach E, Damoiseaux JS. Yoga Effects on Brain Health: A Systematic Review of the Current Literature. Brain Plast. 2019 Dec 26;5(1):105-122. doi: 10.3233/BPL-190084.

    PubMed 31970064
  • Sengupta P. Health Impacts of Yoga and Pranayama: A State-of-the-Art Review. Int J Prev Med. 2012 Jul;3(7):444-58.

    PubMed 22891145

Questions about this trial

What is this clinical trial studying?

A study testing Yoga-Pranayama and Exercise in people with Muscle Aches and Stress, run by Istanbul Gelisim University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 18 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle Tone (Hz) (time frame: During enrollment and after 4 week intervention.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07770139, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Aug 2026.

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