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

2 november 2026 uppdaterad av: 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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Beräknad)

46

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • Rekrytering
        • Riaz Mansoor Trust Hospital
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 40 år (Vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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).

Experimentell: 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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
NPRS (Numeric Pain Rating Scale)
Tidsram: 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)
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

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Utredare

  • Huvudutredare: Ali Raza, Riphah International University

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

28 oktober 2026

Primärt slutförande (Beräknad)

1 december 2026

Avslutad studie (Beräknad)

10 januari 2027

Studieregistreringsdatum

Först inskickad

2 november 2026

Först inskickad som uppfyllde QC-kriterierna

2 november 2026

Första postat (Faktisk)

6 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

6 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

2 november 2026

Senast verifierad

1 november 2026

Mer information

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