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

8. september 2026 opdateret af: 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.

Studieoversigt

Status

Ikke rekrutterer endnu

Intervention / Behandling

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

30

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: Tuba MADEN, Association professor
  • Telefonnummer: +90 531 934 02 49
  • E-mail: tmaden@gantep.edu.tr

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Craniovertebral (Tragus) Angle
Tidsramme: 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
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Static and Dynamic Postural Balance
Tidsramme: 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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Erhan KIZMAZ, University of Gaziantep

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

15. september 2026

Primær færdiggørelse (Anslået)

15. oktober 2026

Studieafslutning (Anslået)

30. oktober 2026

Datoer for studieregistrering

Først indsendt

8. september 2026

Først indsendt, der opfyldte QC-kriterier

8. september 2026

Først opslået (Faktiske)

11. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

11. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • Rigid taping

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

IPD-planbeskrivelse

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

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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