Effects of Active Release Technique Versus Stecco Facial Manipulation in Patient With Chronic Non-specific Neck Pain
21 juillet 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Interventionnel
Inscription (Estimé)
48
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Sumrod Akram
- Numéro de téléphone: 03324806143
- E-mail: samrood.akram@riphah.edu.pk
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
Non
La description
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.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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
|
|
Comparateur actif: 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. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Numeric pain rate scale
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
2. Universal Goniometer
Délai: 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)
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Fatima Nadeem, MSPT*, Riphah International University
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- Sarig-Bahat H. Evidence for exercise therapy in mechanical neck disorders. Man Ther. 2003 Feb;8(1):10-20. doi: 10.1054/math.2002.0480.
- Kazeminasab S, Nejadghaderi SA, Amiri P, Pourfathi H, Araj-Khodaei M, Sullman MJM, Kolahi AA, Safiri S. Neck pain: global epidemiology, trends and risk factors. BMC Musculoskelet Disord. 2022 Jan 3;23(1):26. doi: 10.1186/s12891-021-04957-4.
- Al-Khazali HM, Kroll LS, Ashina H, Melo-Carrillo A, Burstein R, Amin FM, Ashina S. Neck pain and headache: Pathophysiology, treatments and future directions. Musculoskelet Sci Pract. 2023 Aug;66:102804. doi: 10.1016/j.msksp.2023.102804. Epub 2023 Jun 16.
- Prablek M, Gadot R, Xu DS, Ropper AE. Neck Pain: Differential Diagnosis and Management. Neurol Clin. 2023 Feb;41(1):77-85. doi: 10.1016/j.ncl.2022.07.003. Epub 2022 Oct 29.
- Frouzanian M, Shirdel SS, Meskar H, Shahrezaee M, Chamanara M, Ghanbarpour Juybari A, et al. Muscle Morphology and Its Role in Chronic Neck Pain: A Review Article. Translational Health Reports. 2025;1(1):1-11.
- Kaiser JT, Reddy V, Launico MV, Lugo-Pico JG. Anatomy, Head and Neck: Cervical Vertebrae. 2023 Oct 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK539734/
- Khired Z. The Prevalence of and Factors Associated With Neck Pain Among Jazan Adult Population. Cureus. 2022 Aug 14;14(8):e28008. doi: 10.7759/cureus.28008. eCollection 2022 Aug.
- Ko T, Jeong U, Lee K. Effects of the Inclusion Thoracic Mobilization into Cranio-Cervical Flexor Exercise in Patients with Chronic Neck Pain. Journal of physical therapy science. 2010;22(1):87-91.
- Rajkumar RP. The influence of cultural and religious factors on cross-national variations in the prevalence of chronic back and neck pain: an analysis of data from the global burden of disease 2019 study. Front Pain Res (Lausanne). 2023 May 25;4:1189432. doi: 10.3389/fpain.2023.1189432. eCollection 2023.
- Shah DH, Shukla YU. Effect of craniocervical flexion training in mechanical neck pain on proprioception, endurance and pain-an interventional study. 2020.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 juillet 2026
Achèvement primaire (Estimé)
30 novembre 2026
Achèvement de l'étude (Estimé)
30 décembre 2026
Dates d'inscription aux études
Première soumission
21 juillet 2026
Première soumission répondant aux critères de contrôle qualité
21 juillet 2026
Première publication (Réel)
24 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
24 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
21 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- REC/RCR & AHS/25/0138 Fatima-N
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .