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Kendall Versus Janda's Approach Along With Diaphragmatic Breathing Exercises in Upper Crossed Syndrome

21 de julio de 2026 actualizado por: Riphah International University

Comparative Effects of Kendall Versus Janda's Approach Along With Diaphragmatic Breathing Exercises on Pain, Chest Expansion, Cranio Vertebral Angle, and Disability in Upper Crossed Syndrome

Upper Crossed Syndrome (UCS) is a postural imbalance in the upper body characterized by shortened and tight muscles in the front and upper back, while weak muscles in the back and neck are stretched and underactive. This imbalance can lead to forward head posture, rounded shoulders, and increased spinal curves, causing pain, headaches, and reduced range of motion. The study aims to compare the effects of Kendall exercises with Janda's Approach along with Diaphragmatic breathing exercises on pain, chest expansion, craniovertebral angle, and disability in upper crossed syndrome.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

This randomized clinical trial study will be conducted at Central Hospital and Anwer's Polyclinic, Sialkot. We will include 50 patients (25 in each group) of Upper Crossed Syndrome with an age range of 30-50 years, both male and female will be included. Group A will be provided Kendall Exercises with Diaphragmatic breathing exercises, and Group B will receive Janda's with diaphragmatic breathing exercises. Both interventions will be administered for 45 minutes per session, three times per week, for a total duration of six weeks. Outcome measures will include NPRS for pain, Neck Disability Index for disability, Universal goniometer for cranio vertebral angle, and a measuring tape for thoracic expansion will be used. The collected data will be analyzed in the Statistical Package for the Social Sciences (SPSS) 26.0 version. If the data is normally distributed, then a parametric if not normally distributed than a nonparametric test will be applied.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

50

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

  • Nombre: Amna Zia, PhD*
  • Número de teléfono: 03244686993
  • Correo electrónico: amna.zia@kemu.edu.pk

Ubicaciones de estudio

    • Punjab Province
      • Sialkot, Punjab Province, Pakistán
        • Reclutamiento
        • Anwars Polyclinic
        • Contacto:
          • Shaban Anwar, MS-OMPT
          • Número de teléfono: 0332 8609425
          • Correo electrónico: shani_gh85@yahoo.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

Age between 30 to 50 years old Both male and female are included, Craniovertebral angle less than 50°, Rounded shoulders (on photogrammetry)

Exclusion Criteria:

  • Cervical trauma or surgery Congenital scoliosis Spasmodic torticollis Any tumor or trauma History of surgical procedures on neck or lower back Disc issues in neck or lower back

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Kendall exercises
Kendall exercisesare a set of physical therapy movements designed to correct postural faults like Forward Head Posture (FHP), kyphosis, and rounded shoulders. They focus on correcting muscle imbalances through targeted stretching and strengthening.

Stretching: Pectoralis, Upper Trapezius, Levator Scapulae (2 sets of 20 sec each) Strengthening: Scapular retractors with Thera band (2 sets of10 reps), Chin tucks (2 sets of 10 reps), Diaphragmatic breathing (4 mins) Strengthening: Add isometric cervical flexors (5 sec hold with 5 reps),, Chin tucks & scapular retractors (3 sets of 10 reps) Strengthening: Add scapular squeeze (5 sec hold of 5 reps), Emphasize postural control during exercises Strengthening: Functional posture tasks (e.g., seated posture with resistance), Maintain 15 reps of 3 sets

Anterior (Wall Slides), Deep Neck Flexors - 2 sets of 10 reps Diaphragmatic breathing (4 mins), Neck Flexor Hold: 30 sec × 3 sets Add Dumbbell Shrugs, Table Pushes - 3 sets of 10 reps Add Serratus Anterior Upper Cuts (3 sets of 10 reps) strengthening increased to 12-15 reps per set (all muscle groups). Functional integration: Posture tasks during daily movement

Comparador activo: Janda's Approach
Janda's approach is a functional rehabilitation method focusing on how the central nervous system controls muscles and movement. It emphasizes correcting muscle imbalances-where some muscles are overly tight and others are weak or inhibited-to alleviate chronic pain

Stretching: Levator scapulae, Upper Trapezius, Pectoralis (doorway/towel) - 2 sets × 30 sec each, Strengthening: Middle & Lower Trapezius, Serratus Anterior (Wall Slides), Deep Neck Flexors - 2 sets × 10 reps, Diaphragmatic breathing (4 mins) Neck Flexor Hold: 30 sec × 3 sets Add Dumbbell Shrugs, Table Pushes 3 sets × 10 reps Add Serratus Anterior Upper Cuts (3 sets × 10 reps) strengthening increased to 12-15 reps per set (all muscle groups). Maintain 3 sets of stretching.

Functional integration: Posture tasks during daily movement (e.g., reaching, sitting)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
NUMERIC PAIN RATE SCALE (NPRS) for pain
Periodo de tiempo: upto 6 weeks
It is a self-reported scale that measures pain intensity on a scale from 0 (no pain) to 10 (worst possible pain). It is widely used in musculoskeletal conditions for monitoring pain levels over time. The NPRS has demonstrated high validity (r = 0.85 with VAS) and excellent test-retest reliability (ICC = 0.92-0.96). The MCID for NPRS is generally considered to be 2 points, indicating a meaningful improvement or worsening in pain perception
upto 6 weeks
NECK DISABILITY INDEX (NDI)
Periodo de tiempo: upto 6 weeks
It is a validated questionnaire consisting of 10 items that assess the functional impact of neck pain on daily activities such as personal care, work, driving, and recreation. It is specific to cervical conditions. The NDI has strong content validity, with excellent internal consistency (α = 0.87) and test-retest reliability (ICC = 0.89). The MCID for NDI has been reported to range from 5 to 7 points, representing a clinically important change in neck-related disability
upto 6 weeks
UNIVERSAL GONIOMETER for ROM
Periodo de tiempo: Upto 6 weeks
It is used to measure the craniovertebral angle (CVA), an objective indicator of forward head posture in individuals. A CVA less than 50° typically indicates abnormal posture. This tool shows good validity and excellent intra-rater reliability (ICC = 0.80-0.98) for cervical spine angle measurements. While an exact MCID for CVA is not firmly established, a change of 3-5 degrees is often considered clinically meaningful in postural correction studies
Upto 6 weeks
MEASURING TAPE
Periodo de tiempo: Upto 6 weeks
t is a simple and cost-effective tool used to assess chest expansion, which reflects thoracic mobility and respiratory function. The measurement is taken by placing the tape around the chest at the level of the fourth intercostal space during full inhalation and exhalation. It has acceptable criterion validity and demonstrates high intra-rater reliability (ICC = 0.91-0.94), making it suitable for tracking changes in chest mobility during postural or breathing interventions. The MCID for chest expansion is not universally defined, but an increase of 0.5 to 1.0 cm is generally considered clinically relevant in pulmonary and postural rehabilitation contexts
Upto 6 weeks

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Amna Zia, PhD*, King Edward Medical University
  • Investigador principal: Kinza Saif, Riphah International University, Lahore

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

20 de junio de 2026

Finalización primaria (Estimado)

20 de agosto de 2026

Finalización del estudio (Estimado)

20 de septiembre de 2026

Fechas de registro del estudio

Enviado por primera vez

21 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

21 de julio de 2026

Publicado por primera vez (Actual)

24 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

24 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

21 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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