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RecruitingNCT06846697Updated Sep 9, 2025

Effects of Hatha Yoga and Reformer Pilates on Hyperkyphosis

An interventional study of Home-based Exercise and Hatha Yoga Group in Hyperkyphosis, sponsored by Izmir Democracy University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-09-09.

Sponsored by Izmir Democracy University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Feb 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Apr 2025; still recruiting 1 year 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The vertebral column is an S-shaped structure that carries the body weight and transmits it to the feet. Kyphosis, a natural curvature of the spine, can increase with poor posture and muscle weakness, leading to postural kyphosis. This condition results in forward head positioning, rounded shoulders, and scapular winging, causing back pain, poor posture, balance issues, and respiratory difficulties. With technological advances, poor posture habits have become more common, especially in adolescents. Kyphosis can also affect balance, walking speed, and increase the risk of falls in older adults. Exercises like Hatha yoga and reformer Pilates are effective methods for improving posture, muscle strength, and quality of life. The aim of this study is to compare the effects of Hatha yoga and reformer Pilates exercises on posture, pain, balance, quality of life, body image, and respiratory function in individuals with hyperkyphosis.

Read the detailed description

The vertebral column is an S-shaped structure that supports the weight of the upper extremities, head, and neck, transmitting this load to the pelvis and ultimately to the feet. It consists of 34-35 vertebrae, including cervical, thoracic, lumbar, sacral, and coccygeal vertebrae. The cervical and lumbar regions form concave curves (lordosis), while the thoracic and sacral-coccygeal regions form convex curves (kyphosis). The arrangement of the vertebral column in the sagittal plane enables individuals to perform activities with minimal energy expenditure. Kyphosis is the angular and physiological posture formed by the spine and surrounding muscles, which includes the vertebrae and intervertebral discs.This angle is commonly assessed using the Cobb angle in lateral radiographs, with the angle between the lines drawn perpendicular to the 4th-5th thoracic vertebrae and the 12th thoracic vertebrae being measured. Postural kyphosis is defined as an increase in existing spinal curvature due to muscle weakness and poor posture, and it is considered a more flexible deformity compared to other types of kyphosis.The mechanical changes associated with postural kyphosis can impact various functions. The head in kyphotic posture moves forward, altering cervical alignment. This causes the cervical vertebrae to shift anteriorly, leading to compensatory rounding of the shoulders and scapular winging.Factors such as prolonged sitting at desks, poor posture, inadequate furniture, physical inactivity, and heavy school bags contribute to increased muscle spasms and weakened soft tissues, aggravating kyphotic posture. Additionally, technological advancements, especially the widespread use of computers and smartphones, have led to poor postural habits in individuals, particularly adolescents.Rapid growth during adolescence can also cause abnormal spinal flexion, negatively affecting organ development and increasing the kyphosis angle.A study conducted in 2024 showed that corrective exercises combined with active diaphragmatic breathing led to improvements in chest pain and respiratory function in postmenopausal women after a 12-week program.Postural kyphosis is often asymptomatic, but it can result in a visible hunchback, poor posture, back and neck pain, tension, and sensitivity in the spine.In postural kyphosis, the individual can actively or passively correct the posture, but the curvature is flexible. Structural deformities in the spine do not occur. Incorrect postures increase stress on the joints, impairing their function and leading to pain and edema in the discs.Inadequate posture also strains bones, muscles, and ligaments, leading to pain and negatively impacting the position and function of internal organs.Balance refers to the ability to maintain the center of mass within the limits of a base of support during functional activities, utilizing vestibular, visual, and proprioceptive senses. It is classified into static balance, where the center of mass remains stable in a fixed position, and dynamic balance, which involves maintaining balance during movement. Literature indicates that individuals with increased kyphosis experience balance impairments, but postural kyphosis is not routinely assessed for balance.Some studies suggest that kyphosis negatively impacts physical function, balance, and mortality, while others have found no significant link between kyphosis and balance. Research has shown that kyphosis in older women is associated with slower walking speeds, increased body sway, balance issues, and higher fall rates.However, clinical exercises combined with breathing techniques have demonstrated improvements in quality of life and kyphosis angles.Postural kyphosis can impact both physical and psychological well-being, as it affects an individual's appearance. In young individuals, the normal thoracic kyphosis angle is between 20° and 40°, with angles over 45° considered hyperkyphosis.Exercise positively influences both mental and physical health. In adolescence, body image is crucial, and postural deviations often reflect emotional states, with extension positions fostering happiness and confidence, while flexion positions are associated with sadness.Respiration involves coordinated muscle activity. Although inspiration primarily occurs through diaphragmatic muscle activity, additional inspiratory muscles are engaged during deep inspiration. These muscles assist in expanding and contracting the thoracic cavity and contribute to stabilizing the thorax and abdomen.Postural changes in the body and shoulder girdle directly affect thoracic and diaphragm movements, influencing respiratory function. Restrictions in thoracic expansion or diaphragm movement, such as those caused by hyperkyphosis and scapular winging, limit respiratory capacity.Hyperkyphosis can lead to restrictive pulmonary dysfunction, similar to scoliosis, and increases the antero-posterior diameter of the thorax, reducing lung capacity.Studies have shown that hyperkyphosis is associated with decreased pulmonary function and lung volumes.Conservative treatments are the first line of management for postural kyphosis. Manual therapy techniques,postural correction exercises,postural taping,orthotics and the Schroth method are commonly used. Prevention of postural kyphosis begins in childhood with the teaching of proper posture, supporting exercises, muscle strengthening, and spinal alignment.Yoga and Pilates exercises are among the methods used to address these issues.Multidisciplinary treatment approaches are recommended in complementary therapies, addressing patients not only from a bio-psycho-social perspective but also through a bio-mental-physical-psycho-social understanding. Yoga, a mind-body exercise, is often recommended in group therapies. Originating in India over 4,000 years ago, yoga has developed over time to promote both physical strength and spiritual awareness. Various types of yoga, such as Hatha yoga, are similar to physiotherapy practices.Yoga incorporates postures (asanas), breathing exercises (pranayama), and meditation to improve flexibility, strength, and relaxation.Pilates, developed by Joseph Pilates in the 1900s, focuses on improving spinal stability, breathing control, and kinesthetic awareness, promoting both muscle relaxation and mental relaxation. Clinical Pilates is used in rehabilitation for both healthy individuals and those with various medical conditions.Research has shown that Pilates improves flexibility, reduces pain, and enhances quality of life and functional capacity.Studies also suggest that Pilates and yoga improve posture and balance in individuals with hyperkyphosis, although research comparing both approaches is limited.The aim of this study is to compare the effects of Hatha yoga and reformer Pilates exercises on posture, pain, balance, quality of life, body image, body composition, and respiratory function in individuals with hyperkyphosis.

02

Conditions studied

  • Hyperkyphosis

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Keywords

  • Hatha Yoga
  • Reformer Pilates
03

In context

Kyphosis

132 studies on the registry are indexed under Kyphosis; 31 are open to participants now.

This study's planned enrollment of 30 is below the median of 44 across 82 interventional studies indexed under Kyphosis.

Browse Kyphosis studies →

Lead sponsor

Izmir Democracy University is the lead sponsor of 78 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Postural hyperkyphosis
  • Not receiving physiotherapy in the last 6 months

Exclusion criteria

Exclusion Criteria:

  • Exercise is not indicated
  • Communication problems
  • Having a concomitant orthopaedic disorder
  • The presence of a concomitant neurological disorder
  • Presence of concomitant cardiopulmonary disease
  • Presence of recurrent infection
  • Presence of open wound and/or incision
  • Presence of other spinal conditions such as scoliosis
  • Being diagnosed with kyphosis other than postural kyphosis in the classification system
  • Previously undergone a related surgery
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Other
    Control group

    This group will be given a home programme. They will be asked to do the exercises regularly and fulfil the recommendations given and will be asked to come to the control at the end of 8 weeks. During this period, individuals will be followed up weekly by telephone.

    Other: Home-based Exercise

  • Experimental
    Hatha Yoga Group

    Participants in this group, who will also be given a home programme, will participate in Hatha yoga exercises 3 times a week for a total of 8 weeks with a session duration of 45 minutes, accompanied by a physiotherapist with a yoga instructor certificate. In this group, Hatha yoga exercises will be applied by focusing on postural control and respiration during exercise.

    Other: Home-based Exercise · Other: Hatha Yoga Group

  • Experimental
    Reformer Pilates Group

    In this group, which will be given a home programme, participants will perform the exercises 3 times a week for a total of 8 weeks with a session duration of 45 minutes, accompanied by a physiotherapist with a pilates instructor certificate.In this group, which will be given a home programme, participants will perform the exercises 3 times a week for a total of 8 weeks with a session duration of 45 minutes, accompanied by a physiotherapist with a pilates instructor certificate. In this group, reformer pilates exercises will be applied by focusing on postural control during exercise.

    Other: Home-based Exercise · Other: Reformer Pilates Group

Interventions

  • OtherHome-based Exercise

    The subjects in this group will be given the exercises included in the Physical Activity guideline of the Ministry of Health as a home programme.

    Also known as: HBE

  • OtherHatha Yoga Group

    The sessions will begin with the classic sun salutation series (Suryanamaskar) consisting of 12 basic poses of yoga. The sun salutation series will be used as a warm-up for 10 minutes. After warming up, postures aimed at stretching the front group muscles of the body and strengthening the back group muscles will be preferred. In the cooling phase, the session will be ended by relaxing with Savasana pose for 10 minutes.

    Also known as: HYG

  • OtherReformer Pilates Group

    Exercise sessions will start with the foot series and the starting position on the back will be preferred. This series, which is progressed by maintaining the body composition, is considered as a warm-up exercise of the body. Then, the body is continued with exercise series targeting the thoracic region and core region.

    Also known as: RPG

06

What researchers measure

Primary outcomes

  1. New York Posture Evaluation Scale

    The New York Posture Evaluation Scale was first published in 1958. It evaluates the body in 13 different parts in terms of posture changes that may occur. If the posture is correct, 5 points are given, 3 points if it is moderately impaired, and 1 point if it is severely impaired. The total score obtained as a result of the test varies between 13-65 points. A high score means that the posture is good.

    Time frame: At baseline and after 8 weeks

  2. Measurement of the degree of kyphosis with Flexicurve

    Flexicurve will be used to determine the degree of hyperkyphosis. Flexicurve, a noninvasive method, is recommended as a practical and affordable tool for monitoring age-related spinal degenerative processes and curvature changes. One end of the Flexicurve is placed on the bony prominence of the cervical seventh (C7) vertebra and caudally along the spine to the thoracic twelfth vertebra. The mould is then removed from the spine and the shape transferred to paper. Showing the relationship between the length and width of the thorax; Values are obtained according to the formula (width / length) x 100

    Time frame: At baseline and after 8 weeks

  3. Determination of the distance between the occiput and the wall

    It is a practical method widely used for screening and monitoring hyperkyphosis. The individual's back and heels should be as close to the wall as possible and the head should remain in a natural position. Hyperkyphosis is considered to be present if the occiput does not touch the wall when the back and heels are against the wall and the head is facing forwards. The degree of hyperkyphosis is assessed by measuring the distance between the occiput and the wall. The severity of hyperkyphosis is classified as mild (≤5 cm), moderate (5.1-8 cm) and severe (\>8 cm).

    Time frame: At baseline and after 8 weeks

  4. Determination of the distance between wall C7

    There are also studies suggesting that it would be more appropriate to use C7 in the measurement because it is closer and adjacent to the thoracic vertebrae than the occiput. Due to the close location of C7 to the thoracic vertebrae, errors that may be encountered when the participant moves his/her head will be prevented. The measurement is performed with the back, heels and sacrum against the wall, in as upright a posture as possible and looking forwards. The distance of the spinous process of C7 perpendicular to the wall is measured using two rulers. According to the test results, the severity of hyperkyphosis is expressed in three different levels: mild (≤ 5 cm), moderate (5.1- 8 cm) and severe (\> 8 cm).

    Time frame: At baseline and after 8 weeks

  5. Visual Analogue Scale

    Perceived pain ranges from no pain to extreme pain. For pain intensity according to the VAS, 'no pain' is graded as 0 points and 'worst possible pain' is graded as 10 points.

    Time frame: At baseline and after 8 weeks

  6. Timed balance test

    In this test, the duration of standing on one and two legs with eyes open and closed is analysed. It is a static balance test

    Time frame: At baseline and after 8 weeks

  7. Flamingo balance test

    It is a test that measures the duration of static balance in seconds within a one-minute evaluation process. The tool used as an auxiliary material is fixed on the floor. The person conducting the research sits facing the person with the stopwatch. The second observer stands next to the person to help ensure the balance of the person and to see the number of errors in the instrument. One foot of the person stays in the air during this test and when this foot touches the ground or when the person drops this foot completely, the error is recorded and the stopwatch is stopped. After the balance is restored, the stopwatch is restarted and the best score is taken and recorded as the test score. If the person makes fifteen or more errors within 30 seconds after the balance is restored, the test score is reflected as 0.

    Time frame: At baseline and after 8 weeks

  8. Timed up and go test

    This test requires a chair, a stopwatch and a three-metre walking space. The test starts with sitting on a chair, the individual gets up with a warning, walks 3 metres, returns and sits down. It is a test used in dynamic balance assessment.

    Time frame: At baseline and after 8 weeks

  9. Functional reach test

    With the help of a tape measure mounted on the wall, the ability of the subjects to reach without losing their balance is evaluated. It is a test used in dynamic balance assessment.

    Time frame: At baseline and after 8 weeks

  10. Nottingham Health Profile (NHP)

    It is used to assess quality of life. The questionnaire consists of 38 items. It evaluates six dimensions of quality of life including energy; 3 items, pain; 8 items, emotional reactions; 9 items, sleep; 5 items, social isolation; 5 items, physical activity; 8 items. Each section is scored between 0-100, '0' indicates the best health status, while 100 points indicates the worst health status.

    Time frame: At baseline and after 8 weeks

  11. Body Image Assessment

    It will be evaluated with the Multidimensional Body-Image Self-Relationship Scale (MBSRI). This scale is a scale that evaluates the body image of the individual in terms of self-attitudinal aspects. The scale also includes sub-headings that include evaluations of the individual's satisfaction with body image, physical capacity and health status. The scale consists of seven subheadings and 57 items in total. The subheadings generally provide psychological and physical evaluations. In the scale, emotional-cognitive-behavioural evaluations are made on the psychological side and physical appearance-physical competence and biological integrity evaluations are made on the physical side. A maximum score of 285 and a minimum score of 57 can be obtained from the scale.

    Time frame: At baseline and after 8 weeks

  12. Pulmonary Function Test (SFT)

    In our study, SFT measurements will be performed with COSMED Pony FX device (Italy, 2011). Within the scope of the measurement rules, it will be ensured that the subjects have not eaten for at least 2 hours, have not drunk alcohol for at least 4 hours and have not smoked for at least 24 hours. In the test performed in the sitting position, the subjects will be asked to breathe normally for 4 or 5 times, then to make a deep inspiration, followed by a forced, rapid and deep expiration to release all the air. At least three repeated measurements will be performed and the measurement with the highest value in the sum of FEV1 and FVC recommended by ATS will be recorded.

    Time frame: At baseline and after 8 weeks

  13. Chest circumference measurement

    It is performed to evaluate thoracic expansion, chest wall mobility and respiratory type. A bendable, non-elastic tape measure not wider than 7 mm is preferred and measurements are made with feet shoulder-width apart and body weight equally distributed on both feet. In addition, the arms should be slightly abducted for comfortable measurement. In our study, measurements will be performed from three different regions: axillary (4th costal level), epigastric (xiphoid process level) and subcostal (9th costal level) during maximal inspiration, maximal expiration and normal respiratory phase using a tape measure in standing position. The measurements will be repeated three times and the highest value will be recorded. Then, the difference between maximal inspiration and expiration will be found and recorded separately for each region.

    Time frame: At baseline and after 8 weeks

  14. Total body weight measurement

    Total body weight measurement will be performed with a Tanita BC-700 (Tanita-Japan) body analyzer as weight in kilograms.

    Time frame: At baseline and after 8 weeks

  15. Height measurement

    Height in meters will be measured with a height measuring tape.

    Time frame: At baseline and after 8 weeks

  16. Body mass index calculation

    Weight and height will be combined to report BMI in kg/m\^2).

    Time frame: At baseline and after 8 weeks

  17. Lower extremity fat percentage measurement

    Lower extremity fat percentage will be measured using a Tanita BC-700 (Tanita-Japan) body analyzer.

    Time frame: At baseline and after 8 weeks

  18. Total body fat percentage measurement

    Total body fat percentage measurement will be measured using a Tanita BC-700 (Tanita-Japan) body analyzer.

    Time frame: At baseline and after 8 weeks

  19. Lower extremity muscle percentage measurement

    Lower extremity muscle percentage measurement will be measured using a Tanita BC-700 (Tanita-Japan) body analyzer.

    Time frame: At baseline and after 8 weeks

  20. Total body muscle percentage measurement

    Total body muscle percentage measurement will be measured using a Tanita BC-700 (Tanita-Japan) body analyzer.

    Time frame: At baseline and after 8 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2025 (actual). Primary completion is estimated for Feb 2026, 9 months after the start.

Of 56 non-industry interventional studies with no phase under Kyphosis, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 30. This study's planned 9 months is close to that.

Counting every sponsor, half of 58 studies reached it within 9 months; a quarter within 4 and three quarters within 30.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 5, 2025
First posted
Feb 26, 2025
StartActual
Apr 30, 2025
Primary completionEst.
Feb 15, 2026
CompletionEst.
Jun 15, 2026
Last update
Sep 9, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 9, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06846697
Lead sponsor
Izmir Democracy University
Responsible party
Betül Taşpınar (Prof. Dr., Izmir Democracy University) — Principal investigator
First posted
Feb 26, 2025
Start date
Apr 30, 2025
Primary completion
Feb 15, 2026 (estimated)
Completion
Jun 15, 2026 (estimated)
Last update
Sep 9, 2025

Study contacts

Betül Taspinar, Prof. Dr.
Contact
ptbetul@gmail.com
+90 506 680 44 26
Ayşe Akkuş, Msc. Pt.
Contact
akkusayse300@gmail.com.tr
+90 555 572 38 93
Onur Engin, Assist.Prof.
principal investigator · Izmir Democracy University
Ferruh Taspinar, Prof.Dr.
principal investigator · Izmir Democracy University

Oversight

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

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