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L'essai clinique NCT06875856 pour Nonspecific Neck Pain est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
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Effects of Cailliet and Kendall Exercises in Nonspecific Neck Pain

En recrutement
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L'étude clinique NCT06875856 est un essai interventionnel pour Nonspecific Neck Pain. Son statut actuel est : en recrutement. L'étude a débuté le 22 janvier 2025 et vise à recruter 32 participants. Dirigé par l'Université internationale Riphah, l'essai devrait être terminé d'ici le 15 septembre 2025. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 13 mars 2025.
Résumé succinct
Objective of study will be to compare effects of Cailliet and Kendall exercises on pain, functional movement and disability in non-specific neck pain.This randomized clinical trial will be conducted at Good Hands Physiotherapy Clinic, Shahdara Lahore. Sample size of study will be 36. Participants will be randomly divided into two groups Group A and Group B. We will include patients with age group between 25 to 40 years, both genders having localized pain or stiffness in cervical spine for more than 3 months after exclusion of upper limb radiculopathy. Group A will receive Kendall exercises regime and Group B will receive Cailliet exercises regime. Both groups will receive baseline treatment including hot pack and Transcutaneous Electric Nerve Stimulation (TENS). Short term effects would be assessed after treatment for 3 sessions per week on alternate days for 4 weeks. Patients will be assessed by Numeric pain rating scale (NPRS) for pain, Selective Functional Movement Assessment (SFMA) for functional movement and Neck Disability Index (NDI) Urdu version for Disability. Analysis will be done by statistical package for social sciences SPSS 25.
Description détaillée
Pain felt in an area circumscribed superiorly by the superior nuchal line, laterally by the neck's lateral borders, and inferiorly by an imagined transverse line passing through the T1 spinous process is defined as neck pain. An acute or chronic cervical and shoulder girdle issue originating from the occiput of the head to the spine of the scapula, with or without limiting cervical range of motion, and unrelated to any past history of infection or fracture can be characterized as non-specific neck pain. One of the most common musculoskeletal issues that impairs general population function and results in disability is neck pain. The cervical spine is a complicated biomechanical system made up of at least 20 pairs of muscles, many of which have similar roles, and countless degrees of flexibility for each joint. However, the etiology and basic pathology of neck pain are still unknown. Around the world, 330 million people experience some form of neck pain with mean estimates of 7.6% prevalence (range, 5.9-38.7%), 37% annual prevalence (range, 16.7-75%), and 48.5% lifetime prevalence (range, 14.2-71%).

There have been contradictory findings from earlier studies about the optimal management of neck pain. While some contend that exercise leads to greater results, others support the efficacy of conventional therapy. Comparing the short-term benefits of the exercise programs designed by Cailliet and Kendall, in order to ascertain which method produces better results in terms of symptom relief and pain reduction. By getting empirical data on the short-term impacts of exercise treatments, the study will advance evidence-based practice. Healthcare practitioners can rely on this information to make well-informed decisions and recommendations because it will provide scientific proof on their safety and efficacy. This will support the use of a more standardized and empirically supported approach in the treatment of generalized neck pain symptoms associated with the neck musculature.

Titre officiel

Comparative Effects of Cailliet and Kendall Exercises on Pain, Functional Movement and Disability in Nonspecific Neck Pain: Randomized Control Trial

Conditions
Nonspecific Neck Pain
Publications
Articles scientifiques et travaux de recherche publiés sur cet essai clinique:
Autres identifiants de l'essai
  • REC/RCR & AHS/24/0151
Numéro NCT
Date de début (réel)
2025-01-22
Dernière mise à jour publiée
2025-03-13
Date de fin (estimée)
2025-09-15
Inscription (estimée)
32
Type d'essai
Interventionnel
PHASE
N/A
Statut
En recrutement
Mots clés
Cailliet exercises, Kendall exercises, Neck pain
Objectif principal
Traitement
Plan d'attribution
Randomisé
Modèle d'intervention
Parallèle
Masquage
Simple aveugle
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
ExpérimentalGroup A: Kendall exercises program
Group A will receive Kendall exercises program with baseline treatment.
Kendall Exercises
1. Positioning supine with the chin tucked in and lifting the head for 2 to 8 sec to strengthen deep cervical flexors. 2. Maintaining a sitting posture, with hands on the occipital region, and flexed spine while moving head downwards to stretch cervical extensors, maintaining an upright posture. 3. Keep the resistance band circling with strong support and stretching it with the upper limbs of both sides so that there is full retraction of the scapula to strengthen retractors of the shoulder. 4. Stretching the pectoralis major and minor while keeping the patient's hands-on the occipital region and standing behind the patient and pulling both elbows backward to target the bilateral pectoralis muscles
Comparateur actifGroup B: Cailliet exercises program
Group B will receive Cailliet exercises program with baseline treatment.
Cailliet Exercises
The intervention of group B will include baseline treatment, followed by maneuvers, including: Neck Cailliet exercise using isometric contractions against the prisoner to the maximum that ends with relaxation and continued with stretching. Each posture was maintained for 30 s and 3 sets of 10 repetitions were performed with 3 sessions per week on alternate days for 4 weeks.
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
Numeric Pain Rating Scale
Pain intensity will be assessed by NPRS. The NPRS has shown to have moderate to high test-retest reliability, ranging from 0.67 to 0.96. The NPRS is shown to have convergent validity between 0.79 and 0.95. The 11-point NPRS (intervals from 0-10) is used to quantify pain intensity; 0 represents no pain, and 10 represent the worst possible agony. Zero indicates absence of pain while 5 indicate moderate pain and 10 indicate unbearable pain. The patient is asked to mark a number on the scale. At the baseline assessment, after 3 weeks and finally at the end of the intervention program, the NPRS scores will be recorded.
4 weeks
Selective Functional Movement Assessment (SFMA)
The Selective Functional Movement Assessment (SFMA) is a popular assessment tool used to observe and detect components of dysfunctional movement patterns. The goal of the assessment is to identify impairments throughout the kinetic chain that may be contributing to movement dysfunction and/or pain. Kappa coefficients for intra-rater reliability ranged from 0.21-1.00, while % absolute agreement ranged from 0.64-1.00.
4 weeks
Neck Disability Index (NDI) for disability
The neck disability index (NDI) is one of the most commonly used questionnaires to measure neck pain and disability. One study reported that the NDI is a multidimensional construct that measures a broader concept than disability. Each item is scored out of 5 for a maximum total score of 50. Care should be taken in reporting the score as either out of 50 or as a percentage out of 100. A score of 22% or more is considered a significant activities of daily living disability.
4 weeks
Critères d'éligibilité

Âges éligibles
Adulte
Âge minimum
18 Years
Sexes éligibles
Tous
  • Age group between 18 to 40 years
  • Both gender male and female
  • Individuals having localized pain or stiffness in spine or both combined between C3 and C7 without upper limb radiculopathy
  • Negative Spurling's test, traction test, upper limb tension test, and shoulder abduction test.
  • Pain reported on NPRS Moderate score in neck region for more than 3 months
  • Neck Disability Index (NDI) score of 0-10 points out of 50 score

  • Tuberculosis, carcinoma, heart disease, and osteoporosis
  • Neural disorders due to prolapsed intervertebral disc
  • Any trauma, localized infection or history of surgery in cervical spine region in last 6 months
  • Upper motor neuron disease, cervical stenosis, and metabolic diseases in bone and joint
  • Hyper flexibility, Open sores
  • Ongoing radiotherapy, chemotherapy, steroid therapy, or anticoagulants
  • Psychiatric diseases such as phobia/obsession and depression
  • Allergy to hot pack
Riphah International University logoUniversité internationale Riphah
Contact central de l'essai
Contact: Imran Amjad, PHD*, 03324390125, [email protected]
Contact: Imran Amjad, PHD*, 0515481826, [email protected]
1 Centres de l'essai dans 1 pays

Punjab Province

Good hands physiotherapy clinic, Lahore, Punjab Province, 54000, Pakistan
Ghulam Fatima, PhD*, Contact, 03034073057, [email protected]
Hafsa Mushtaq, MS*, Investigateur principal
En recrutement