- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07716137
Effects of Instrument Assisted Soft Tissue Mobilization on Sensory Motor Mismatch in Text Neck Syndrome.
16 juli 2026 uppdaterad av: 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.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Beräknad)
66
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Ramsha Tariq, MS OMPT
- Telefonnummer: 03315251422
- E-post: ramsha.tariq@riphah.edu.pk
Studieorter
-
-
Punjab Province
-
Rawalpindi, Punjab Province, Pakistan
- Railway General Hospital
-
Kontakt:
- Ramsha Tariq, MS OMPT
- Telefonnummer: 0331-5251422
- E-post: ramsha.tariq@riphah.edu.pk
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Nej
Beskrivning
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.)
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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).
|
|
Aktiv komparator: 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).
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Fukuda stepping test - vestibular deviation
Tidsram: 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
Tidsram: 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
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Cervical Joint Position Error (JPE) Test
Tidsram: 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
|
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Berg Balance Scale (BBS)
Tidsram: 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
Tidsram: 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
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Ramsha Tariq, MS OMPT, Riphah International University
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- 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.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
15 juli 2026
Primärt slutförande (Beräknad)
15 december 2026
Avslutad studie (Beräknad)
25 december 2026
Studieregistreringsdatum
Först inskickad
16 juli 2026
Först inskickad som uppfyllde QC-kriterierna
16 juli 2026
Första postat (Faktisk)
21 juli 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
21 juli 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
16 juli 2026
Senast verifierad
1 juli 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- RCRAHS-ISB/REC/MS-PT/02433
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
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Nej
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