CClinicalTrials.gg
Status unknownNCT05409521Updated Jun 8, 2022

Immediate Effects of Kinesio Taping Applied to the Thoracic Region in Adult Individuals

An interventional study of Kinesio taping and Placebo taping in Kinesio Taping and Healthy Adults, sponsored by Ankara Yildirim Beyazıt University. Status unknown. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-06-08.

Sponsored by Ankara Yildirim Beyazıt University · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Jun 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

The purpose of the study is to search immediate effects of kinesio taping applied to the thoracic region on proprioception, posture and trunk muscle endurance in adult individuals.

Read the detailed description

Kinesio tape applications are one of the frequently used interventions within the scope of physiotherapy and rehabilitation. Kinesio taping is a non-invasive treatment method performed for several reasons such as reducing pain, relieving abnormal muscle and fascia tension and correcting biomechanical alignment. Kinesio taping consists of muscle, fascia, ligament, mechanic, functional and lymphatic correction techniques depending on therapeutic purposes.

Although kinesio tape applications on different regions such as abdomen or neck may have positive effects on posture, proprioception and trunk muscle endurance, there has not been found any study searching the effectiveness of kinesio taping applied to thoracal region on posture, proprioception and trunk muscle endurance in adult individuals. Thus, there is a need to investigate this issue.

02

Conditions studied

  • Kinesio Taping
  • Healthy Adults
03

In context

Lead sponsor

Ankara Yildirim Beyazıt University is the lead sponsor of 228 studies on the registry; 53 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged between 18 and 35 years,
  • Volunteer to paticipate to the study

Exclusion criteria

Exclusion Criteria:

  • Musculoskeletal pain problems in the last 6 months
  • Spinal fractures
  • History related to spinal surgery
  • Spinal deformity (scoliosis etc)
  • Any chronic disease (cancer, diabetes mellitus, hypertension etc. )
  • Body mass index>35 kg/m2
  • Mental or psychologic problems
  • Any dermatologic disease
  • Allergy to kinesio tape
05

Study design

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

Study arms

  • Experimental
    Tape Group

    Kinesio taping will be applied on thoracic region

    Other: Kinesio taping

  • Placebo comparator
    Placebo Group

    Placebo taping will be applied on arm region

    Other: Placebo taping

Interventions

  • OtherKinesio taping

    Kinesio taping with the mechanical correction technique will be applied on the thoracic region

  • OtherPlacebo taping

    Placebo taping with no tension and technique will be applied on the arm

06

What researchers measure

Primary outcomes

  1. Trunk position sense

    Inclinometer will be positioned at spinous process of 4th thoracic vertebrae during trunk position sense assessment. Subject will be retreated to neutral position and asked to come back taught position while eyes closed. Test will be repeated 3 times and angle of deviation from 30 degree flexion position will be recorded and the average of the results will be taken.

    Time frame: immediately after the intervention

Secondary outcomes

  1. Joint position sense of cervical spine

    Whereas one side of inclinometer positioned at apex of head, other side will be positioned at spinous process of 7th cervical vertebrae during assessment of cervical spine joint position sense. Subject' head will be brought to 300 flexion from neutral position and will be wanted to learn this position. Subject will be retreated to neutral position and asked to come back taught position while eyes closed. Test will be repeated 3 times and angle of deviation from 300 flexion position will be recorded to subject assessment sheet each repetition and average of the results will be taken.

    Time frame: immediately after the intervention

  2. Thoracic kyphosis

    The assessment of thoracic kyphosis will be done using dual digital inclinometer. In order to evaluate thoracic kyphosis, the angle between first thoracic vertebrae and 12th thoracic vertebrae will be measured. As the angle increases, the degree of kyphosis increases.

    Time frame: immediately after the intervention

  3. Head-neck posture

    Head-neck posture will be evaluated with the measurement of cranio- vertebral angle. The angle between 7th cervical vertebrae and tragus will be measured with goniometer to determine cranio- vertebral angle. As the angle decreases, the forward tilt of the head increases.

    Time frame: immediately after the intervention

  4. Trunk extensor muscle endurance

    Trunk extensor muscle endurance will be evaluated with Biering- Sorensen test.Subjects will be asked to lie down on a bed in prone position while trunk positioned outside of the bed until SIAS (spina illiaca anterior superior) level. Lower extremity will be stabilised by researchers. Initially subjects will be asked to extend their trunk to horizontal position (bed level) and then cross their arms on the chest and hold at this position as long as they would. The duration that subjects stayed at the horizontal position without any movement will be calculated with chronometer and recorded as second.

    Time frame: immediately after the intervention

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 8, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05409521
Lead sponsor
Ankara Yildirim Beyazıt University
Responsible party
seyda toprak celenay (associate professor, Ankara Yildirim Beyazıt University) — Principal investigator
First posted
Jun 8, 2022
Start date
Jun 30, 2022 (estimated)
Primary completion
Aug 30, 2022 (estimated)
Completion
Sep 30, 2022 (estimated)
Last update
Jun 8, 2022

Study contacts

Seyda Toprak Celenay
Contact
sydtoprak@hotmail.com
+90312 906 1000
Seyda Toprak Celenay
principal investigator · Ankara Yildirim Beyazıt University

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion