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Healthy Young Adults Who Are Health Care Workers at Haydarpaşa Numune Training and Research HospitalNCT06729281

The Effect of Kinesio Taping on Posture in Healthy Young Adults

A study testing kinesio tape in people with Healthy Young Adults Who Are Health Care Workers at Haydarpaşa Numune Training and Research Hospital, run by Elem Yorulmaz at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Healthy young adults who are health care workers at Haydarpasa Numune Training and Research Hospital will be included in the study considering the inclusion and exclusion criteria. Demographic data such as age, gender, height, weight will be recorded. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
What is being tested?
kinesio tape
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteTurkey (Türkiye)
Study dates
20 Mar 2024to 31 Dec 2024
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 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Health workers
  • Over 18 and under 40
  • Visual analog scale (VAS) < 4 for muscle pain
  • Inactive (category 1) and minimally active (category 2) according to the international physical activity survey
  • Healthcare workers without cognitive deficits who can take verbal instructions

Who cannot join

  • Diagnosed disc herniation with or without spinal deformity
  • Bone abnormality and peripheral symptoms
  • Infectious or inflammatory arthropathies
  • History of joint replacement surgery,
  • History of spinal surgery
  • Need for assistive devices for ambulation
Show all 14Show fewer
  • irregular hypertension
  • Uncontrolled diabetes mellitus
  • Presence of neurological disease
  • History of malignancy
  • Uncontrolled cardiopulmonary disease
  • Pregnancy
  • Morbid obesity (Body mass index > 35)
  • Having fibromyalgia syndrome

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Haydarpaşa Numune Training and Research Hospital Physical Medicine and Rehabilitation Clinic

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Healthy young adults who are health care workers at Haydarpasa Numune Training and Research Hospital will be included in the study considering the inclusion and exclusion criteria. Demographic data such as age, gender, height, weight will be recorded. Thoracic kyphosis and lumbar lordosis angles of the participants will be recorded with Goniometer pro application at the beginning. Spinal muscle thickness including the back extensor muscle group will be measured from the thoracic and lumbar regions with ultrasound by a specialist with clinical experience for ultrasound. Measurement will be made at T8 level for thoracic region and L3 level for lumbar region. They will be evaluated with the Nottingham health profile.

A total of 78 people will be included in the study and will be randomly divided into two groups as intervention + exercise and exercise only group. Randomization will be done by closed envelope method. Kinesiobanting will be applied to the intervention group for 4 weeks, with the posture correction technique on Mondays, and the kinesiobant application will be applied once a week for 4 sessions in total, to be removed on Friday. Both groups will be given a 40-minute posture exercise program based on clinical experience, to be performed every other day, i.e. 4 times a week for 12 weeks. Patients will be given an exercise follow-up chart and will be called once a week and followed up for 12 weeks. In the intervention group, thoracic kyphosis and lumbar lordosis angle measurements with Goniometer pro application will be examined at 30.minute at baseline, Week 4 and Week 12, while in the exercise only group they will be examined at baseline, Week 4 and Week 12. Ultrasound measurement of spinal muscle thickness will be performed at baseline and at Week 12 in both groups. Nottingham Health Profile will be performed at baseline, Week 4 and Week 12 in both groups. Differences within and between groups will be analyzed statistically.

Being tested
kinesio tape

What participants receive

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

  • kinesio tapeDevice

    The application of kinesio tape is a relatively new method, first developed in 1973 by Kenzo Kase in Japan, also known as elastic bandage, which has become popular in the last 10 years following announcements at major events such as the Olympic Games.

Study groups in NCT06729281
Study groupRoleWhat they receive
exerciseNo interventionRegular exercise is also among the factors affecting the formation of posture. A regular and systematic exercise program can change the curvatures of the spine in the sagittal plane.
exercise and kinesio tapingOtherRegular exercise is also among the factors affecting the formation of posture. A regular and systematic exercise program can change the curvatures of the spine in the sagittal plane. + Kinesiotaping
Receives: Device: kinesio tape

What is being measured

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

  1. Thoracic kyphosis and lumbar lordosis measurements with Goniometer Pro Application

    Thoracic kyphosis and lumbar lordosis angle measurements with Goniometer pro application will be examined at 30 minutes at baseline, Week 4 and Week 12, whereas only in the exercise group will be examined at baseline, Week 4 and Week 12.

    Measured: 1. month and 3. month

  2. Spinal muscle thickness measurements with Ultrasound

    Ultrasound measurement of spinal muscle thickness will be performed with Mindray brand ultrasound in both groups at baseline and at week 12, with measurements indicated in millimetres.

    Measured: 1. month and 3. month

Secondary outcomes (1)
  1. Nottingham Health Profile

    Nottingham Health Profile will be performed at baseline, Week 4 and Week 12 in both groups. Differences within and between groups will be analyzed statistically

    Measured: 1.month and 3. month

Timeline

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

  1. First posted11 Dec 2024
  2. Study start20 Mar 2024
  3. Primary completion1 Jul 2024
  4. Study completion31 Dec 2024 (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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06729281
Sponsor's protocol ID
E-62977267-903.99-23331179
Status last verified
Nov 2024
First submitted
21 Nov 2024
Last updated
11 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Pai S A, Zhang H, Shewchuk JR, Al Omran B, Street J, Wilson D, Doroudi M, Brown SHM, Oxland TR. Quantitative identification and segmentation repeatability of thoracic spinal muscle morphology. JOR Spine. 2020 Jul 1;3(3):e1103. doi: 10.1002/jsp2.1103. eCollection 2020 Sep.

    PubMed 33015576

Questions about this trial

What is this clinical trial studying?

A study testing kinesio tape in people with Healthy Young Adults Who Are Health Care Workers at Haydarpaşa Numune Training and Research Hospital, run by Elem Yorulmaz 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 5 inclusion and 14 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: under way, not looking for participants, as of the sponsor's last update on 11 Dec 2024. 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?

Thoracic kyphosis and lumbar lordosis measurements with Goniometer Pro Application (time frame: 1. month and 3. month). The study lists 2 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 NCT06729281, which also lists 1 linked publication.

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 11 Dec 2024; AzTrials last refreshed its copy on 7 Nov 2026.

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