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Effects of Active Release Technique Versus Stecco Facial Manipulation in Patient With Chronic Non-specific Neck Pain

21. juli 2026 oppdatert av: Riphah International University

Effects of Active Release Technique Versus Stecco Facial Manipulation on Pain, Craniovertebral Angle, and Functional Disability in Patients With Chronic Non-specific Neck Pain.

Non-specific pain that originates from the superior nuchal line and extends to the first thoracic vertebrae. It is exacerbated by sustained neck postures, neck movements or cervical muscle palpation. Neck pain is a work-related musculoskeletal disease that can arise during prolonged or high-intensity activity. Increasingly, individuals seek medical attention for discomfort in the neck, upper extremities, and head caused by chronic tension. Neck discomfort is often caused by mechanical dysfunction that restricts joint movement inside the joint capsule. Active Release Technique(ART) is a manual release of tight soft tissue which targets on SCM, levator scapulae, suboccipital and Upper trapezius. Stecco Fascial Manipulation is an efficient manual soft tissue treatment method that particularly address in the areas of myofascial pain and discomfort, locomotor issues, and posture dysfunction. The aim of this study is to treat the patients having chronic non specific neck pain through the Active Release Technique (ART) and Stecco Facial Manipulation and to compare their effects that can affect cervical flexibility and to improve the symptom parameters of the regarding individual.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

The current study will be Randomized Clinical Trial. Inclusion criteria for this study is the individual with chronic non specific neck pain between the age group of 20-40yr. Patient with any history of trauma or surgery in cervical region and any other cervical pathology will be excluded from the study. A sample of 44 individual with CNSNP will be selected from both genders. Tools used for the Data collection will be Numeric Pain Rating Scale(NPRS), Neck Disability Index(NDI) and Goniometer. Participants will be measured before and after treatment to assess changes. Interventions are carried out 5 days in a week for one hour daily. In this study descriptive statistical tools will used to analyze the data. Data will be analyzed through SPSS version 21.

Studietype

Intervensjonell

Registrering (Antatt)

48

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Individuals of both genders
  • Age between 20-40yrs(19).
  • Neck pain persisting for more than 3 months
  • Neck Disability Index (NDI) score between 10-30) (20).

Exclusion Criteria:

  • Patients with history of trauma or surgery were excluded.

    • Cervical pain patients with radiculopathy were excluded.
    • Patients diagnosed cases of rheumatoid arthritis, or any systemic musculoskeletal disorders were excluded.
    • Patients use of muscle relaxants or undergoing any other physiotherapy for neck issues in the past 3 months were excluded.
    • Patients with cervical disc herniation or whiplash injuries were excluded.
    • Pregnancy or known hormonal conditions affecting musculoskeletal system were excluded.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: GROUP A: Active Release Technique
Group A will be treated with the active release technique
Active release technique is a manual release of tight soft tissue that targets the upper trapezius, SCM, Levator scapulae, and sub occipital muscle to improve posture and reduce tightness and pain
Aktiv komparator: GROUP B: Stecco Method
Group B was treated with stecco method

Stecco method, also known as Fascial Manipulation, is a manual therapy technique developed by Luigi Stecco, which focuses on releasing tension and restoring normal glide in the fascial system, especially where myofascial dysfunction is contributing to pain and restriction.

Stecco method is applied specifically to the Levator scapulae, SCM, subocccipital, and upper trapezius muscles .All commonly involved in chronic non-specific neck pain.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Numeric pain rate scale
Tidsramme: upto 6 weeks
The numerical rating scale (0-10), with 0 meaning no pain, and 10 meaning the worst unbearable pain, as measurement of pain intensity.
upto 6 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
2. Universal Goniometer
Tidsramme: upto 6 weeks
Universal goniometer is a popular tool in the clinical and rehabilitation environment to determine the joint angles and evaluate the range of movement (ROM).
upto 6 weeks
Neck Disability index for functional Disability (NDI)
Tidsramme: upto 6 weeks
The Neck Disability Index(NDI) is a questionnaire designed to assess self-rated impairment of the individuals experiencing neck discomfort. It has ten questions on most aspects of daily living, such as the severity of pain, self-care, lifting, reading, and entertainment. This Questionnaire has a reliability of 0.87.The question has six answer options (including 0 (no disability) and 5 (full impairment). The total score ranges 0 to 50 whereby higher scores are going to be a greater impairment. It may also be stated as a percentage (0 to 100%)
upto 6 weeks
Flexion Rotation Test
Tidsramme: upto 6 weeks
Flexion Rotation Test (FRT) a physical examination instrument of specifying the rotation within the upper neck, particularly C1-C2. It helps to identify rotational, and can suggest chronic non specific neck pains or other upper cervical spine dysfunctions.
upto 6 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Fatima Nadeem, MSPT*, Riphah International University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. juli 2026

Primær fullføring (Antatt)

30. november 2026

Studiet fullført (Antatt)

30. desember 2026

Datoer for studieregistrering

Først innsendt

21. juli 2026

Først innsendt som oppfylte QC-kriteriene

21. juli 2026

Først lagt ut (Faktiske)

24. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

24. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

21. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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