Kinesio Taping in Obesity: Breathing and Sleep Implications

ConditionObesity
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorElif Kabasakal

About this trial

Obesity, defined as excessive fat accumulation, is a chronic, complex, and global health issue. It is increasingly prevalent worldwide and is considered a disease that requires treatment. According to recent data, 43% of adults aged 18 and over were classified as overweight, and 16% as obese. In Turkey, a national health survey reported that among individuals aged 15 and above, 20.2% were obese, and 35.6% were in a pre-obese state based on their body mass index (BMI).

The effects of excess weight on health are significant, as weight gain shortens life expectancy and reduces quality of life. Obesity has detrimental effects on many systems, including the respiratory system. It reduces the compliance of the lungs and chest wall, alters respiratory patterns and ventilation-perfusion relationships, impairs gas exchange, and decreases lung volumes. In some individuals, respiratory control is altered due to the effects of adipokines, which can lead to hypoventilation and increased levels of carbon dioxide in the blood (hypercapnia).

Obesity affects the respiratory system both symptomatically (e.g., shortness of breath) and functionally. Respiratory function disorders in individuals with obesity may include decreased functional residual capacity (FRC), expiratory reserve volume (ERV), and, in some cases, reduced total lung capacity (TLC). Additionally, obesity is a health issue that affects sleep quality. There are three proposed bidirectional relationships: obesity causes poor sleep, poor sleep contributes to obesity, and both may coexist. Individuals with obesity often report poor sleep quality and sleep disorders such as sleep apnea.

The primary function of the respiratory system is gas exchange, which is closely related to the mechanical properties of the respiratory pump. The functionality of this pump depends on the interaction of the lungs, abdominal wall, ribs, intercostal muscles, and the diaphragm. In diseases that impair the structure of the diaphragm, improving its function can alleviate symptoms and significantly enhance pulmonary function test results.

Kinesiology taping (KT), an elastic therapeutic taping method, is commonly used for musculoskeletal disorders but has a wide range of clinical applications. Kinesiology tapes are reported to support weak muscles, increase circulation, reduce pain by stimulating the neurological system, provide proprioceptive feedback, and correct joint misalignments. The mechanism by which KT influences muscle strength depends on the application technique, which can either enhance or inhibit muscle activation. The underlying mechanism is explained by the stimulation of sensory-motor and proprioceptive systems, aiming to improve muscle function through enhanced neuromuscular feedback. Kinesiology taping has also shown potential benefits in respiratory conditions by improving diaphragm function, reducing respiratory muscle fatigue, and enhancing overall respiratory mechanics.

Understanding the effects of thoracic kinesiology taping on respiratory function, vital signs, sleep, quality of life, and cognitive functions in individuals with obesity is of great importance for physiotherapists and researchers. The findings from this study may provide valuable insights for developing comprehensive rehabilitation programs and improving the health status of individuals with obesity. Therefore, the aim of this study is to investigate the effects of thoracic kinesiology taping on respiratory functions, respiratory muscle strength, vital signs, sleep, quality of life, and cognitive status in individuals with obesity.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being between 18 and 70 years of age

Being overweight or classified as class 1 or class 2 obese based on BMI

Having the ability to follow instructions and participate in study procedures

Being able to speak and understand Turkish

Disqualifiers

Having an acute or chronic pulmonary or respiratory disease

Having an uncontrolled chronic illness

Having an allergic reaction to kinesiology tape

Refusing to participate in the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Kinesiology Taping

    Other intervention

    For thoracic kinesiology taping (KT), a 5 cm wide, 100% cotton, latex-free elastic tape will be used. Application sites will follow the technique and principles described by Kase. Participants will sit upright in an armless chair with knees at 90° flexion, feet flat on the floor, and arms relaxed. The tape will be applied to the front and back of the body to facilitate respiratory muscles, primarily the diaphragm. On the anterior side, an "I"-shaped strip will be applied with 50-75% tension at the xiphoid process along the linea alba, and the tails will be laid over the subcostal area without tension. Posteriorly, another "I"-shaped strip will be applied from the projection of the 12th thoracic vertebra with 50-75% tension, and the ends placed toward the ribs without tension. Additionally, two more strips will be applied to the upper trapezius region between the neck and acromion bilaterally.

  • Diaphragmatic Breathing Exercises

    Other intervention

    Participants in the control group will receive diaphragmatic breathing exercises. Exercises will be taught and supervised by a physiotherapist. Sessions will be conducted twice weekly for four weeks, and participants will be instructed to continue home practice between sessions.

Treatment groups

36 Participants
are divided into 2 treatment groups
Group A: Kinesiology TapingExperimental treatment 1 intervention
Group B: control groupOther 1 intervention

Trial outcomes

Primary outcomes

1

Forced Vital Capacity (FVC)

Forced Vital Capacity (FVC) will be measured using a portable spirometer (Cosmed Pony FX, Italy) following ATS/ERS guidelines. Results will be recorded in liters and as a percentage of the predicted value.

Time frame
At baseline (before the intervention) and at the end of the 4th week of intervention
2

Forced Expiratory Volume in 1 Second (FEV1)

FEV1 will be assessed using a spirometer (Cosmed Pony FX) under ATS/ERS standards. The measurement will be recorded in liters and as a percentage of the predicted normal value.

Time frame
At baseline (before the intervention) and at the end of the 4th week of intervention
3

FEV1/FVC Ratio

The ratio of FEV1 to FVC (FEV1/FVC) will be calculated to assess airway obstruction. The values will be expressed as a percentage. All procedures will be carried out with standardized spirometry protocols (ATS/ERS) using single-use mouthpieces and filters.

Time frame
At baseline (before the intervention) and at the end of the 4th week of intervention
4

Peak Expiratory Flow (PEF)

PEF will be measured as part of the pulmonary function test using a spirometer. Values will be expressed in liters per second (L/s) and as a percentage of the predicted value. Infection control procedures will include the use of disposable mouthpieces and filters as per device guidelines.

Time frame
At baseline (before the intervention) and at the end of the 4th week of intervention

Secondary outcomes

1

Heart Rate (HR)

Heart rate (HR) will be measured in beats per minute (bpm) using a validated digital pulse oximeter or heart rate monitor. Measurements will be taken at baseline and at the end of the 4th week, as well as daily during the intervention period (upon waking, during the day, and before sleep).

Time frame
Baseline, Week 4 (Post-Intervention), and Daily During Weeks 1-4
2

Oxygen Saturation (SpO₂)

Peripheral oxygen saturation (SpO₂) will be assessed using a digital pulse oximeter. Measurements will be recorded as a percentage and monitored daily during the intervention period, including morning, daytime, and pre-sleep values, along with baseline and end-of-intervention readings.

Time frame
Baseline, Week 4 (Post-Intervention), and Daily During Weeks 1-4
3

Blood Pressure (Systolic and Diastolic)

Systolic and diastolic blood pressure (BP) will be measured in mmHg using an automated upper-arm digital sphygmomanometer. Readings will be obtained at baseline and at the end of Week 4, as well as daily throughout the intervention (morning, daytime, and before bedtime).

Time frame
Baseline, Week 4 (Post-Intervention), and Daily During Weeks 1-4
4

Obesity-Specific Quality of Life Questionnaire (OQOLQ) Total Score

Obesity-specific quality of life will be assessed using the OQOLQ, a validated 17-item scale developed by Patrick et al. Each item is scored on a six-point Likert scale. The scale is unidimensional, and higher total scores indicate poorer quality of life. The validated Turkish version will be used in this study.

Time frame
Baseline and Week 4 (Post-Intervention)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Elif Kabasakal

Lead sponsor

Istinye University

Sponsor institution