Rigid Taping's Effects on Posture and Balance in Office Workers

September 8, 2026 updated by: Erhan KIZMAZ, Pamukkale University

Acute Effects of Rigid Taping on Spinal Alignment, Tragus Angle, Balance in Office Workers: A Spinal Mouse Assessment

This study looks at whether applying a rigid tape to the upper back can immediately improve posture and balance in people who spend long hours sitting at a desk. Thirty office workers will have their head and neck position, spinal posture, and standing balance measured, then the tape will be applied to gently support the upper back and shoulders in a more upright position. The same measurements will be repeated 15 minutes later, while the tape is still in place. The tape is a flexible, skin-safe material commonly used in sports and physical therapy; it contains no medication and is not expected to cause discomfort or side effects. By comparing the measurements taken before and after taping, the researchers hope to learn whether this simple, non-invasive technique can produce an immediate improvement in head and spinal alignment and in balance control. This study looks only at short-term (acute) effects and does not test whether the benefits, if any, last beyond the taping session. The results may help patients and health care providers understand whether taping could serve as a quick, low-risk tool to support better posture during long periods of desk work.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Prolonged sitting and forward-leaning postures during desk-based office work are commonly associated with increased thoracic kyphosis, forward head posture, and reduced postural control. Rigid taping applied to the thoracic region has been proposed as a low-cost, non-invasive method to provide passive postural correction and proprioceptive feedback, but its immediate (acute) effects in office-working populations have not been fully characterized.

This study uses a single-group, pre-post (within-subject) design to evaluate the acute effects of rigid thoracic postural correction taping in office workers. Baseline assessments of craniovertebral alignment, sagittal spinal posture, and standing balance will be obtained, after which rigid tape will be applied by a trained examiner along a standardized pattern over the thoracic spine and shoulder girdle to passively encourage scapular retraction, thoracic extension, and reduced forward head positioning. All baseline measurements will be repeated after a 15-minute period with the tape in place, allowing evaluation of the immediate biomechanical response to the intervention.

The primary hypothesis is that rigid thoracic taping will acutely improve craniovertebral alignment and selected spinal alignment parameters, and may additionally improve dynamic balance. Findings are intended to inform whether rigid taping may serve as a practical, low-risk adjunct for immediate postural support in individuals with prolonged sedentary, desk-based occupational exposure.

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Tuba MADEN, Association professor
  • Phone Number: +90 531 934 02 49
  • Email: tmaden@gantep.edu.tr

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • be an individual who works at least 6 hours a day at a desk
  • not having had any musculoskeletal disorders or orthopedic surgery in the last 6 months
  • not use any postural support

Exclusion Criteria:

  • having been diagnosed with chronic pain or postural deformity in the lower back, upper back, or neck region
  • having structural spinal disorders such as scoliosis, kyphosis, or lordosis
  • having undergone physical therapy or manual therapy within the last 3 months
  • having previously undergone rigid taping
  • pregnancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Rigid taping
Participants in this single-arm study receive rigid thoracic postural correction taping applied by a trained examiner along a standardized pattern over the thoracic spine and shoulder girdle to passively encourage scapular retraction, thoracic extension, and reduced forward head positioning. Outcome measures (craniovertebral angle, spinal alignment, and standing balance) are assessed at baseline (pre-taping) and again after 15 minutes with the tape in place (post-taping), with each participant serving as their own control.
igid thoracic postural correction taping applied bilaterally by a trained examiner, starting from the anterior surface of the humerus and extending to the level of T12, to passively encourage scapular retraction, thoracic extension, and reduced forward head positioning

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Craniovertebral (Tragus) Angle
Time Frame: Baseline and 15 minutes after tape application
Craniovertebral alignment will be assessed using the tragus angle, a validated proxy for forward head posture. An increase in the tragus angle indicates a more neutral (less forward) head position.
Baseline and 15 minutes after tape application
Change in Sagittal Spinal Alignment
Time Frame: Baseline and 15 minutes after tape application
Spinal alignment will be assessed non-invasively using the SpinalMouse device in neutral standing, maximal flexion, and maximal extension postures, yielding segmental angles (sacral/hip, thoracic, lumbar, and inclination).
Baseline and 15 minutes after tape application

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Static and Dynamic Postural Balance
Time Frame: Baseline and 15 minutes after tape application
Postural balance will be assessed using a force platform (ForcePlates) system, with center-of-pressure (COP) parameters including sway area, mean velocity, and displacement in the anteroposterior and mediolateral directions.
Baseline and 15 minutes after tape application

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Erhan KIZMAZ, University of Gaziantep

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 15, 2026

Primary Completion (Estimated)

October 15, 2026

Study Completion (Estimated)

October 30, 2026

Study Registration Dates

First Submitted

September 8, 2026

First Submitted That Met QC Criteria

September 8, 2026

First Posted (Actual)

September 11, 2026

Study Record Updates

Last Update Posted (Actual)

September 11, 2026

Last Update Submitted That Met QC Criteria

September 8, 2026

Last Verified

September 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • Rigid taping

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared, as the informed consent obtained from participants did not include provisions for third-party data sharing.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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