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临床试验/CTRI/2025/06/088851
CTRI/2025/06/088851尚未招募3 期

Effect of scapular stabilizing exercises on craniovertebral angle, grip strength and pinch strength in asymptomatic smartphone addicted users

Dr Vanshika Khurana PT1 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2025年6月30日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
106
试验地点
1
主要终点
Grip strength

研究概览

简要总结

In this study, we will evaluate the effect of scapular stabilizing exercises on craniovertebral angle, grip strength and pinch strength in asymptomatic smartphone addicted users. Pre and post measurements of craniovertebral angle, grip and key pinch strength of smartphone addicted users who are using smartphone for more than 4 hours per day for more than 1 year will be documented. 106 participants will be divided into 2 groups (53 each). Group A will receive scapular stabilizing exercises plus ergonomic educational leaflet for a period of 4 weeks, while group B will receive ergonomic educational leaflet only. Post intervention values of craniovertebral angle, grip strength and pinch strength will be recorded after a period of 4 weeks. The data will be analyzed using appropriate statistical tests.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • •Male and female in the age group 18-40 years.
  • •Smartphone users who have been using smartphone for more than 4 hours for more than 1 year.

排除标准

  • •Participants complaining of pain or symptoms related to any cardiovascular, musculoskeletal or neurological dysfunction in neck or dominant upper extremity that may affect study variables.
  • •Previous history of any injury or congenital or diagnosed disease or surgery which may affect study variables.
  • •Any diagnosed case of malignancy.

结局指标

主要结局

Grip strength

时间窗: At baseline (pre-intervention) and | At 4 weeks (post intervention)

Pinch strength

时间窗: At baseline (pre-intervention) and | At 4 weeks (post intervention)

Craniovertebral angle

时间窗: At baseline (pre-intervention) and | At 4 weeks (post intervention)

次要结局

未报告次要终点

研究者

发起方
Dr Vanshika Khurana PT
申办方类型
Other [self]

研究点 (1)

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