Effect Of Kinesiology Tape On Pain, Posture, Balance And Respiration In Ankylosing Spondylitis

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 years and older
• All sexes
• No healthy volunteers
• Adult, Older adult

Trial locations and contacts

1 site in 1 country.

About this study

Conditions

Ankylosing Spondylitis

Being tested

Kinesio Taping, Exercise

Keywords

Ankylosing Spondylitis, Kinesio Taping, Exercise

Medical subject headings

Spondylitis, Ankylosing, Motor Activity

What participants receive

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

• Kinesio TapingProcedure or surgery

  Kinesiology tapes were applied when the patient was in forward flexion and shoulders were protracted, using functional correction method. Applied without tension at the adhesion point, without any tension in the first 5 from acromioclavicular joint level and then by applying maximum tension and terminating at the lower boundary of costa. Crossing point of the tapes was arranged to be at the lower 1/3 of scapula medial side. Muscle stimulation technique was used to support diaphragm muscle. Origo was xiphoid process, cartilage of 6th costa and lumbar vertebra and insertio was central tendon. Application was made when the patient was standing, with spine at hyperextension, in inspiration and arms in abduction. Tape was applied by following the lower costa curvature from xiphoid process towards lateral. Symmetrically, kinesiology tape was applied dorsally, starting from T12 level and following lower costa curvature.

• ExerciseProcedure or surgery

  Conventional exercises (Joint ROM, spinal extensor strengthening, posture, balance and respiratory exercises) were explained verbally to both groups and video demonstrations were shown. Patients exercised five days a week for six week, in three sets, consisting of 10 repetitions per day. Exercise practices of the patients were routinely monitored and the patients were encouraged to continue exercise program and phone calls were made to follow-up exercises.

What is being measured

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

1. VISUAL ANALOG SCALA

   This is a scale used to assess pain. It consists of numbered lines on a horizontal line from 0 to 10. The patient marks the line to indicate the intensity of the pain they feel. 0 corresponds to no pain, and 10 corresponds to the most severe pain.

   Measured: From enrollment to the end of treatment at 6 weeks

2. Spinal Pain

   The device consists of numbered boxes on a horizontal line from 0 to 10. The patient marks the boxes to indicate the spinal pain they have felt in the last week. 0 corresponds to no pain, and 10 corresponds to the most severe pain.

   Measured: From enrollment to the end of treatment at 6 weeks

3. Nocturnal Spinal Pain

   The system consists of numbered boxes on a horizontal line from 0 to 10. The patient marks the boxes to indicate the nocturnal spinal pain they have felt in the past week. 0 corresponds to no pain, and 10 corresponds to the most severe pain.

   Measured: From enrollment to the end of treatment at 6 weeks

4. Fingertips-Floor Distance

   The patient is asked to stand upright and touch the tip of their finger to the ground without bending their knees. If there is a limitation, the distance between the fingertip and the ground is measured and recorded. For men, up to 10 cm is considered normal. For women, it is zero.

   Measured: From enrollment to the end of treatment at 6 weeks

5. Modified Schober Test Score

   While the patient is standing, a mark is made 10 cm upwards and 5 cm downwards from this prominence. The distance between the two points is 15 cm. The patient performs maximum flexion of their torso. The distance between the two points is measured. 15 cm is subtracted from the measured distance to find the difference. If the difference is less than 5 cm, the test is positive.

   Measured: From enrollment to the end of treatment at 6 weeks

6. BASDAI Score

   This is a disease activity-related scale. It consists of 6 questions. Each question has horizontally numbered boxes from 0 to 10, where 0 means none and 10 means very severe. The patient should answer the questions based on their condition over the past week. The questions cover: weakness/fatigue, neck/back/hip pain, joint pain and swelling, touch and pressure sensitivity, and the severity and duration of morning stiffness. The average of the answers to 2 questions related to morning stiffness is added to the sum of the first 4 questions, and then divided by 5 to obtain a combined score.

   Measured: From enrollment to the end of treatment at 6 weeks

7. BASFI Score

   The purpose of this scale is to determine and monitor physical functioning in patients with AS. It consists of 10 questions in total: 8 items related to the patients' functional anatomy (bending, reaching, changing position, standing, turning, and climbing stairs) and 2 items assessing the patients' skills related to daily living. The scale is numbered horizontally in rows from 0 to 10, where 0 means easy and 10 means impossible.

   Measured: From enrollment to the end of treatment at 6 weeks

8. BASMI Score

   BASMI is a scale used to measure axial skeletal mobility in AS patients and to objectively evaluate clinically significant changes in spinal movement. It was first introduced in 1994 as a 2-point scale. A year later, it was adapted as a 10-point scale, and more recently, its current version as a linear marker has been developed and validated through validation studies.72 It consists of 5 items representing clinical measurements of cervical rotation, tragus-to-wall distance, lumbar flexion (modified Schober), spinal lateral flexion, and maximal intermalleolar distance. Each item is scored between 0 and 10 according to separately defined cut-off values. The ranges are defined as cervical rotation (8.5°-85.0°), tragus-to-wall (10 cm-38 cm), lumbar flexion (7.0 cm-0.7 cm), lumbar lateral flexion (1.2 cm-20 cm), and intermalleolar distance (30 cm-120 cm).

   Measured: From enrollment to the end of treatment at 6 weeks

9. AS Health Assessment Questionnaire

   This test is used to assess the physical function of an individual with AS. It consists of 20 questions across 8 categories: dressing, lying down, standing up, eating, walking, hygiene, daily tasks, and grasping. Patients should answer the questions considering their performance over the past week. A scoring system from 0 to 3 is used, with 4 options: 0; easily able, 3; unable to do at all. The total score is divided by the number of questions answered to obtain the final value.

   Measured: From enrollment to the end of treatment at 6 weeks

10. Chest Expanison Diameter

    The patient is asked to perform maximal inspiration and expiration. During this time, a measurement is taken and recorded at the 4th intercostal space. The difference between these two results, both in centimeters, is calculated to obtain the desired value.

    Measured: From enrollment to the end of treatment at 6 weeks

11. Respiratory Function Test (RFT)

    It is a physiological test that measures airflow as a function of the volume of air taken in and exhaled during respiration and time. Today, it is one of the most basic diagnostic methods frequently used in the diagnosis and monitoring of many lung diseases.

    Dynamic Spirometry It is the first step in respiratory function tests. It is used to evaluate ventilatory capacity. The most important cause of impaired ventilatory capacity is airway obstruction. It is evaluated during forced inspiration and expiration. The measured volume is related to time and expressed with volume-time or flow-volume curves.

    FORCED VITAL CAPACITY (FVC): The volume of air expelled with a forced, rapid, and deep expiration after a deep inspiration.

    Normal: FVC = VC(Vital capacity) Airway obstruction: FVC < VC Normally, 75-80% of the volumes are expelled in the first second. It generally reflects the large airways. It is significantly red

    Measured: From enrollment to the end of treatment at 6 weeks

12. Berg Balance Scale

    The Berg Balance Scale is a test used to assess functional balance. It was developed in 1989 by Katherine Berg to evaluate balance functions in the elderly. The scale is useful in predicting the risk and consequences of falls, in evaluating rehabilitation in hospitalized patients, and in assessing the length of hospital stay.

    It consists of 14 items for performance evaluation. Each item is scored between 0 and 4 according to the patient's ability to meet the distance and time requirements of the test. A score of 4 indicates the ability to complete the task without assistance. The highest score is 56. Scores between 0 and 20 indicate impaired balance, 21-40 indicate acceptable balance, and 41-56 indicate good balance.

    Measured: From enrollment to the end of treatment at 6 weeks

Timeline

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

1. First posted16 Jan 2026
2. Study start1 Apr 2023
3. Primary completion1 Jan 2024
4. Study completion30 Jan 2024

Resources

• Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
• Other trials for Ankylosing SpondylitisStudies of the same condition, open and under way.
• What the trial phases meanHow a treatment moves from first tests in people to approval.

More details

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