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Effects of Alexander Technique in Children With Upper Cross Syndrome.

R

Riphah International University

Status

Enrolling

Conditions

CHILD Syndrome

Treatments

Other: Corrective exercises
Other: Alexander technique

Study type

Interventional

Funder types

Other

Identifiers

NCT07248748
REC/RCR&AHS/SHANZACHAUDHARY

Details and patient eligibility

About

This randomized clinical trial will involve 50 participants aged 13 to 16, recruited from Faisal Hospital Faisalabad and different schools nearby. Participants will be randomly assigned to either the Alexander Technique group, which will include home-based exercises supervised by parents, or a control group performing traditional posture-corrective exercises. The outcomes will be measured using tools such as the Cranio-Vertebral Angle (CVA), Shoulder Protraction Measurement (SPM), Thoracic Kyphotic Angle (TKA), and Visual Analogue Scale (VAS) for pain assessment. The findings are expected to provide insights into the benefits of the Alexander Technique as a therapeutic strategy for addressing UCS and improving overall health outcomes in adolescents. Data collection will be done before and after the intervention. Data will be analyzed through SPSS version 26.00.

Full description

Upper Cross Syndrome (UCS) is a common postural disorder characterized by muscle imbalances resulting from prolonged use of electronic devices, leading to symptoms such as forward head posture, rounded shoulders, and increased thoracic kyphosis. This condition predominantly affects young adults and is associated with discomfort and decreased postural stability, negatively impacting overall physical function. The study aims to investigate the effectiveness of the Alexander Technique (AT) in improving pain levels and range of motion (ROM) in individuals with Upper Cross Syndrome. By focusing on the principles of optimal body use and postural awareness, the Alexander Technique may offer a valuable intervention to alleviate symptoms and enhance Range of motion.

This randomized clinical trial will involve 50 participants aged 13 to 16, recruited from Faisal Hospital Faisalabad and different schools nearby. Participants will be randomly assigned to either the Alexander Technique group, which will include home-based exercises supervised by parents, or a control group performing traditional posture-corrective exercises. The outcomes will be measured using tools such as the Cranio-Vertebral Angle (CVA), Shoulder Protraction Measurement (SPM), Thoracic Kyphotic Angle (TKA), and Visual Analogue Scale (VAS) for pain assessment. The findings are expected to provide insights into the benefits of the Alexander Technique as a therapeutic strategy for addressing UCS and improving overall health outcomes in adolescents. Data collection will be done before and after the intervention. Data will be analyzed through SPSS version 26.00.

Enrollment

36 estimated patients

Sex

All

Ages

13 to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 13 -16
  • School going children

Exclusion criteria

  • Participants with signs of:
  • Fractures
  • Surgeries
  • Joint problems
  • Injuries in the spine
  • Skeletal-muscular imbalances
  • Lower limb cross syndrome abnormal BMI participants engaging in regular physical activity for at least 6 h per week

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

36 participants in 2 patient groups

GROUP A
Active Comparator group
Description:
control group
Treatment:
Other: Corrective exercises
GROUP B
Active Comparator group
Description:
interventional group
Treatment:
Other: Alexander technique

Trial contacts and locations

1

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Central trial contact

Imran Amjad, PhD; Muhammad Asif Javed, MS-PT

Data sourced from clinicaltrials.gov

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