Effect of cervical-scapular stabilization with graded isotonic elastic band exercises on neck pain, disability and posture among female students with text neck syndrome- A Randomized Controlled Trial
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Galgotias University
- Enrollment
- 76
- Locations
- 1
- Primary Endpoint
- Pain, posture and neck disability
Overview
Brief Summary
This randomized controlled trial aims to evaluate the effect of Cervical-scapular stabilization combined with graded isotonic elastic band exercises on neck pain, functional disability, and postural alignment among female students with text neck syndrome. The study will include female participants aged between 18 and 25 years who reports prolonged use of smartphones or digital devices associated with neck pain and forward head posture. Participants will be randomly allocated into two groups. One group will receive cervical-scapular stabilization with elastic band exercises, while the control group will receive conventional physiotherapy. The intervention will be carried out for 6 weeks, and outcome measure such as pain, neck disability index, and postural alignment will be recorded at baseline, 2 weeks, 4 weeks and 6 weeks of intervention. The results will help determine whether combination of cervical - scapular stabilization and elastic band exercises is effective in reducing symptoms and improve posture in female students with text neck syndrome.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 25.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •Female students aged 18 to 25 years Clinical signs of forward head posture and neck pain Average screentime of more than 5 hours a day Pain duration of more than 4 weeks VAS pain score more than or equal to 5.
Exclusion Criteria
- •Cervical spine trauma or deformities Neurological symptoms History of cervical surgery Ongoing physiotherapy treatment for other conditions.
Outcomes
Primary Outcomes
Pain, posture and neck disability
Time Frame: Baseline, 2 weeks, 4 weeks and 6 weeks
Secondary Outcomes
No secondary outcomes reported
Investigators
Poushali Ghosh
Galgotias University