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Effects of Alexander Technique Versus Feldenkrais Somatic Training in Patients With Text Neck Syndrome

2 de noviembre de 2026 actualizado por: Riphah International University

Effects of Alexander Technique Versus Feldenkrais Somatic Training on Pain, Cranio-Vertebral Angle and Disability in Patients With Text Neck Syndrome

in this era, increasing use of smart gadgets such as mobile phones, laptops, computers etc has led to rise in musculoskeletal disorders, particularly Text Neck Syndrome, which is characterized by neck and upper back pain with prolonged neck flexion and forward head posture. Somatic education approaches such as the Alexander Technique and Feldenkrais Method offer alternative strategies by emphasizing postural awareness, movement quality, and neuromuscular re-education rather than repetitive exercise alone. The study will be conducted as a randomized clinical trial and the assessor will be blind. Sample size of 46 subjects will be taken according to inclusion criteria and subjects will be allocated in two groups by computer generator software. Conventional intervention will be received as a standardized treatment protocol in both groups with additional intervention. Group A will receive Alexander technique while Group B will receive Feldenkrais technique. The data will be analyzed using appropriate statistical methods to evaluate the effectiveness of each intervention. This study's results can provide valuable information to healthcare professionals on how to manage Text neck syndrome.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Intervención / Tratamiento

Descripción detallada

PROJECT SUMMARY:

In this modern era, increasing use of smart gadgets such as mobile phones, laptops, computers etc has led to rise in musculoskeletal disorders, particularly Text Neck Syndrome, which is characterized by neck and upper back pain with prolonged neck flexion and forward head posture. Although conventional physiotherapy interventions such as postural correction, strengthening, and stretching have demonstrated benefits; however, persistent symptoms, functional limitations, and reduced treatment adherence remain challenges. Somatic education approaches such as the Alexander Technique and Feldenkrais Method offer alternative strategies by emphasizing postural awareness, movement quality, and neuromuscular re-education rather than repetitive exercise alone. The Alexander Technique focuses on optimizing the head-neck-spine relationship, reducing unnecessary muscle tension, and modifying habitual movement patterns through conscious inhibition and direction, whereas the Feldenkrais Method employs gentle, awareness-based movement lessons and functional integration to enhance sensorimotor organization, proprioception, and movement efficiency. Both approaches may contribute to improved posture, reduced pain and enhanced functional outcomes in individuals with neck pain.

The study will be conducted as a randomized clinical trial and the assessor will be blind. Sample size of 46 subjects will be taken according to inclusion criteria and subjects will be allocated in two groups by computer generator software. Conventional intervention will be received as a standardized treatment protocol in both groups with additional somatic intervention. Group A will receive Alexander technique while Group B will receive Feldenkrais technique. The primary outcomes measured will be pain, disability, and cranio-cervical angle. The study will collect data at baseline and four weeks using validated outcome measures. The data will be analyzed using appropriate statistical methods to evaluate the effectiveness of each intervention. In this study, participants in both groups will receive treatment twice a week, with a total of eight treatment sessions over the four-week study period. The results of the study will provide valuable insights into the efficacy of Alexander technique and Feldenkrais training in managing Text neck syndrome. This study's results can provide valuable information to healthcare professionals on how to manage Text neck syndrome and may contribute to the development of future research in this area.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

46

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

Ubicaciones de estudio

    • Punjab Province
      • Lahore, Punjab Province, Pakistán, 54000
        • Reclutamiento
        • Riaz Mansoor Trust Hospital
        • Contacto:
          • Mehwish Irfan
          • Número de teléfono: +923204435562
          • Correo electrónico: Umine2i2@gmail.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

18 años a 40 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Male and Female are included
  • Age between 18- 40 years age
  • Using smart phone ≥4 hours/day
  • Neck pain duration ≥3 months
  • Neck pain increase by sustained posture
  • NDI score range from >20 points
  • Cranio-vertebral angle ≤ 48°

Exclusion Criteria:

  • Any trauma or injury on cervical and thoracic spine
  • History of cervical spine surgery
  • Specific neck pathologies (cervical disc herniation, radiculopathy, inflammatory conditions, spinal infection and tumor)
  • Congenital Spinal deformity
  • Psychological problem

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: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Alexander Technique

Each patient will receive a total number of eight treatment sessions over a four-week period and each session is about 45 min. There will be 3 sessions in per week. Constructive rest-5 min, Gentle cervical rotation in supine , 4-5 each side, Head and neck release awareness in sitting, Semi supine arm awareness, Sitting Posture Re-education: Ask the patient to hold the phone at eye level, Sitting to standing by Alexander Method, Gentle cervical rotation sitting, Functional Reaching with AT Cues, Stimulated phone use training, Sustained posture awareness drill

TENS (10 min), Hot pack (10 min), Soft tissue mobilization, Grade I, II matland mobilization of cervical spine, AROM (10 reps- 2 sets), Upper trapezius stretch (5 sets, hold for 15-30 sec), Levator Scapulae stretch (5 sets, hold for 15-30 sec), SCM stretch (5 sets, hold for 15-30 sec), Pectoralis major stretch (5 sets, hold for 15-30 sec), Cervical isometrics in flexion, extension and side bending (5-10 sets, hold for 10 sec).

Experimental: Feldenkrais Somatic training

TENS (10 min), Hot pack (10 min), Soft tissue mobilization, Grade I, II matland mobilization of cervical spine, AROM (10 reps- 2 sets), Upper trapezius stretch (5 sets, hold for 15-30 sec), Levator Scapulae stretch (5 sets, hold for 15-30 sec), SCM stretch (5 sets, hold for 15-30 sec), Pectoralis major stretch (5 sets, hold for 15-30 sec), Cervical isometrics in flexion, extension and side bending (5-10 sets, hold for 10 sec).

Each patient will receive a total number of eight treatment sessions over a four-week period and each session is about 45 min. There will be 3 sessions in per week. Body scan in supine, small circles in supine , Chin nodding in supine lying, Jaw-neck awareness (ask the patient to open & close mouth gently), Head turning with shoulder awareness (patient is in supine position, ask the patient to turn head right while noticing left shoulder and move to the alternate sides.), Eye-head coordination (ask the patient to move eyes right first, then head follows then reverse direction.), Side-lying head lift (1 cm), Scapula-neck relationship (patient in standing, ask the patient to gently slide shoulder up/down while head rests and therapist observe neck response.), Thoracic rolling in supine, Pelvic rocking with in supine lying, Standing weight shift + head response, Walking with free neck, Text neck re education

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
NPRS (Numeric Pain Rating Scale)
Periodo de tiempo: From enrollment to end of week 4

Numeric pain rating scale were used to measure the intensity level of the patient's pain. Scale consists of 11 points, ranging from 0 -10. 0 is no pain and 10 is the worst imaginable pain. Subjects select the number that best symbolizes their level of pain.

0= No pain 1-3= Mild pain 4-6= Moderate pain 7-10= severe pain

From enrollment to end of week 4
NDI (Neck Disability Index)
Periodo de tiempo: From enrolment to end of week 4

The Neck Disability Index is the most general measure for evaluating self-perceived disability in patients with neck pain. Each question has six options to rate the disability level from 0 (no disability) to 5 (total disability). The numeric responses for each question are summed for a total score between 0 and 50.

No disability= 0 - 4 Mild= 5 - 14 Moderate= 15 - 24 Severe= 25 - 34 Complete Disability = 35 - 50

From enrolment to end of week 4
Photogrammetry for Cranio-vertebral angle
Periodo de tiempo: From enrollment to end of week 4

Photogrammetry is a most commonly used noninvasive tool to assess cranio-vertebral angle or posture alignment. Participants will be asked to stand or seated in normal or relaxed posture. Lateral photographs were taken and mark the spinous process of C7 and tragus of ear. The angle between the line joining from tragus to C7 spinous process and horizontal line will be measured with the help of Image J. Software to determine cranio-vertebral angle.

From enrollment to end of week 4

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Ali Raza, Riphah International University

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.

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)

28 de octubre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2026

Finalización del estudio (Estimado)

10 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

2 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

2 de noviembre de 2026

Publicado por primera vez (Actual)

6 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de noviembre de 2026

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

2 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • REC/RCR & AHS/25/0186

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

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .