CTRI/2025/06/089823尚未招募1 期
Efficacy of Multimodal Physiotherapy on Pain, Joint Position Sense and Gait in Patients With Neck Pain: A Randomized Controlled Trial
Nitte Deemed to be University1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年7月15日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale (VAS)
研究概览
简要总结
The primary purpose of this randomized controlled trial is to evaluate the effectiveness of multimodal physiotherapy compared to traditional physiotherapy in patients with neck pain. The study aims to assess and compare improvements in pain intensity, joint position sense, and gait parameters between the two groups. It is hypothesized that multimodal physiotherapy will be more effective in reducing pain, improving cervical proprioception, and enhancing gait than traditional physiotherapy alone.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Open Label
入排标准
- 年龄范围
- 19.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Adults aged from nineteen years to sixty-five years.
- •Individuals who have been clinically diagnosed with neck pain.
- •Participants who report a pain intensity greater than thirty millimeters on the Visual Analogue Scale at the start of the study.
- •Participants who demonstrate a joint position error of five degrees or more during the baseline assessment of neck proprioception.
排除标准
- •Exclusion criteria History of trauma or injury to the cervical spine.
- •Individuals with diagnosed vestibular disorders or severe impairments in Visual-Vestibular Interaction.
- •Individuals with diagnosed vestibular disorders Presence of severe psychiatric disorders affecting compliance.
- •Involvement in other therapeutic interventions for neck pain during the study period.
- •Any contraindications to exercise or electrotherapy.
- •No previous neck surgery or invasive interventions within the last 6 months.
- •No neurological deficits or severe comorbidities affecting participation.
结局指标
主要结局
Visual Analogue Scale (VAS)
时间窗: Baseline (Pre-intervention) | After 4 weeks (Post-intervention)
次要结局
- Joint Position Sense Error Test(Gait Analysis)
研究者
研究点 (1)
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