Effects of Instrument Assisted Soft Tissue Mobilization on Sensory Motor Mismatch in Text Neck Syndrome.
16 juli 2026 bijgewerkt door: Riphah International University
Text Neck Syndrome is increasingly common in young adults due to prolonged smartphone use and is linked to postural changes and impaired sensorimotor control.
Although its effects on visual-vestibular integration, balance, and proprioception are still unknown, Instrument-Assisted Soft Tissue Mobilization (IASTM) may improve neuromuscular function by enhancing afferent input and mechanoreceptor stimulation.
This study investigates whether IASTM can improve sensorimotor processing in individuals with Text Neck Syndrome.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This study aims to bridge that gap by investigating whether mechanical soft tissue stimulation can influence sensorimotor processing, balance and proprioception in individuals with Text Neck Syndrome.
The study design used for this literature would be Randomized Control Trial, consisting of two groups; Experimental group (IASTM) & Control group (conventional treatment).
Study sample is 66 participants meeting the inclusion criteria chosen according to non-probability convenient sampling.
33 participants will be to each of the control and interventional group.
IASTM is applied using stainless steel Garston tools along with the conventional therapy for experimental group while control group will be given conventional therapy only.
Two sessions will be given per week and total eight sessions will be given over the period of one month.
And results will be recorded at the base level, at fourth session and then at 8th session for both groups.
Studietype
Ingrijpend
Inschrijving (Geschat)
66
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Ramsha Tariq, MS OMPT
- Telefoonnummer: 03315251422
- E-mail: ramsha.tariq@riphah.edu.pk
Studie Locaties
-
-
Punjab Province
-
Rawalpindi, Punjab Province, Pakistan
- Railway General Hospital
-
Contact:
- Ramsha Tariq, MS OMPT
- Telefoonnummer: 0331-5251422
- E-mail: ramsha.tariq@riphah.edu.pk
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Adults aged 18-30
- Using the phone or computer for 3 h or more per day.
The presence of 3 out of the following 6 symptoms:
- Neck pain (recurrent history of neck pain in the previous 4 months, a pain level greater than or equal to 4/10 on the NPRS (moderate pain))
- Upper back pain,
- Shoulder pain,
- Headache (tension type headache due to tension in sub-occipitals)
- Insomnia
- Tingling and numbness in the upper limbs
- Cranio-vertebral angle (CVA) <48-50° on digital photogrammetry
- Individuals having sensory-motor mismatch (positive Fukuda test:>45° degrees, abnormal dynamic visual acuity, positive cervical JPE>4.5°)
- Voluntary participation
Exclusion Criteria:
- History of cervical spine surgery, trauma, or fracture
- Any diagnosed neurological disorders (cervical radiculopathy, peripheral neuropathy, fibromyalgia, etc.)
- Any diagnosed MSK related issue (torticollis, scoliosis, diagnosed disc prolapse, stenosis, herniation, spondylolisthesis, osteoporosis, etc.)
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Experimental: IASTM + Conventional Physiotherapy
Participants will receive Instrument-Assisted Soft Tissue Mobilization (IASTM) in addition to conventional physiotherapy.
IASTM will be applied to the upper trapezius, levator scapulae, sternocleidomastoid, suboccipital muscles, and cervical extensors using stainless steel instruments.
Conventional therapy will include cervical isometric exercises, deep cervical flexor activation, scapular strengthening exercises, stretching exercises, thoracic extension exercises, and postural re-education.
Treatment will be administered twice weekly for 4 weeks (8 sessions total).
|
Participants will receive Instrument-Assisted Soft Tissue Mobilization (IASTM) in addition to conventional physiotherapy.
IASTM will be applied to the upper trapezius, levator scapulae, sternocleidomastoid, suboccipital muscles, and cervical extensors using stainless steel instruments.
Conventional therapy will include cervical isometric exercises, deep cervical flexor activation, scapular strengthening exercises, stretching exercises, thoracic extension exercises, and postural re-education.
Treatment will be administered twice weekly for 4 weeks (8 sessions total).
|
|
Actieve vergelijker: Conventional Physiotherapy (Exercise-based) (control group)
Participants will receive conventional physiotherapy consisting of cervical isometric strengthening exercises, deep cervical flexor activation exercises, scapular strengthening exercises, stretching exercises, thoracic extension exercises, and postural re-education.
Treatment will be administered twice weekly for 4 weeks (8 sessions total).
|
Participants will receive conventional physiotherapy consisting of cervical isometric strengthening exercises, deep cervical flexor activation exercises, scapular strengthening exercises, stretching exercises, thoracic extension exercises, and postural re-education.
Treatment will be administered twice weekly for 4 weeks (8 sessions total).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Fukuda stepping test - vestibular deviation
Tijdsspanne: 4 weeks
|
• Evaluates vestibulospinal reflex integrity by observing angular deviation during stepping in place with eyes closed.
It indicates asymmetry in vestibular or sensory motor control.
The FST is based on vestibulospinal reflex and widely used for evaluation of labyrinthine function.
The significant displacement or rotation (more than 45°) is considered abnormal and suggest a vestibular imbalance.
|
4 weeks
|
|
Dynamic visual acuity test
Tijdsspanne: 4 weeks
|
● Assesses visual vestibular interaction by measuring visual acuity during active head movement.
It detects gaze instability caused by impaired vestibulo- ocular reflex (VOR) and sensory-motor mismatch.
A difference of two or more lines on eye-chart than seen in static visual acuity is considered abnormal.
|
4 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Cervical Joint Position Error (JPE) Test
Tijdsspanne: 4 weeks
|
A clinical test used to assess cervical proprioceptive accuracy by measuring a person's ability to relocate their head to a neutral position after active neck movement.
It quantifies repositioning errors that may result from altered cervical joint and muscle spindle function, commonly seen in neck pain and after muscle fatigue.
The deviation of 7.1 cm is equivalent to 4.5° thus, the joint position error of greater than 4.5° is considered as positive.
|
4 weeks
|
|
Berg Balance Scale (BBS)
Tijdsspanne: 4 weeks
|
A 14-item observational tool called the Berg Balance Scale (BBS) is used to evaluate both static and dynamic balance while doing functional tasks.
Its overall score is 56, where a score of less than 45 indicates a higher danger of falling.
|
4 weeks
|
|
Universal Goniometer
Tijdsspanne: 4 weeks
|
A manual instrument used to assess active cervical spine range of motion (flexion, extension, rotation, and side-bending).
It provides quantitative data for cervical mobility changes.
|
4 weeks
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Ramsha Tariq, MS OMPT, Riphah International University
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Algemene publicaties
- Mylonas K, Angelopoulos P, Billis E, Tsepis E, Fousekis K. Combining targeted instrument-assisted soft tissue mobilization applications and neuromuscular exercises can correct forward head posture and improve the functionality of patients with mechanical neck pain: a randomized control study. BMC Musculoskelet Disord. 2021 Feb 21;22(1):212. doi: 10.1186/s12891-021-04080-4.
- Piruta J, Kulak W. Physiotherapy in Text Neck Syndrome: A Scoping Review of Current Evidence and Future Directions. J Clin Med. 2025 Feb 19;14(4):1386. doi: 10.3390/jcm14041386.
- Kaya M, Ucgun H, Denizoglu Kulli H. The effect of proprioceptive neuromuscular facilitation on individuals with text neck syndrome: A randomized controlled study. Medicine (Baltimore). 2024 Jul 26;103(30):e38716. doi: 10.1097/MD.0000000000038716.
- 1. Kumar N. Latest Smartphone Usage Statistics (2025 Data & Trends). Demandsage [Internet]. 2025.
- Tsantili AR, Chrysikos D, Troupis T. Text Neck Syndrome: Disentangling a New Epidemic. Acta Med Acad. 2022 Aug;51(2):123-127. doi: 10.5644/ama2006-124.380.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
15 juli 2026
Primaire voltooiing (Geschat)
15 december 2026
Studie voltooiing (Geschat)
25 december 2026
Studieregistratiedata
Eerst ingediend
16 juli 2026
Eerst ingediend dat voldeed aan de QC-criteria
16 juli 2026
Eerst geplaatst (Werkelijk)
21 juli 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
21 juli 2026
Laatste update ingediend die voldeed aan QC-criteria
16 juli 2026
Laatst geverifieerd
1 juli 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- RCRAHS-ISB/REC/MS-PT/02433
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .