跳至主要内容
临床试验/CTRI/2025/07/091501
CTRI/2025/07/091501尚未招募不适用

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

Galgotias University1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
76
试验地点
1
主要终点
Pain, posture and neck disability

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 25.00 Year(s)(—)
性别
Female

入选标准

  • 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.

排除标准

  • Cervical spine trauma or deformities Neurological symptoms History of cervical surgery Ongoing physiotherapy treatment for other conditions.

结局指标

主要结局

Pain, posture and neck disability

时间窗: Baseline, 2 weeks, 4 weeks and 6 weeks

次要结局

未报告次要终点

研究者

发起方
Galgotias University
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Poushali Ghosh

Galgotias University

研究点 (1)

Loading locations...

相似试验