TCTR20240522004尚未招募1 期
EFFECTS OF ERGONOMIC WORKSTATION INTERVENTIONS AND DEEP NECK FLEXORS EXERCISE ON NECK MUSCLE PERFORMANCE, FORWARD HEAD POSTURE, AND NECK DISABILITY IN BANKERS WITH NON-SPECIFIC NECK PAI
/A0 个研究点目标入组 22 人开始时间: 2024年5月22日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 22
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 Years 至 40 Years(—)
- 性别
- All
入选标准
- •1. Neck pain that mostly worsens owing to the adaption of improper posture during work and can be decreased by postural correction.
- •2. Symptoms continuing for approximately more than three months, including those who
- •complained of neck pain at least once a week over the previous three months.
- •3. Mild (VAS scores 1 to 4) to moderate (VAS ratings 4 to 6) Neck Pain Severity.
- •4. More than 1 year of work experience.
- •5.CVA less than 48 degrees.
- •6. Women will be expected to work at a computer for atleast four hours per day, while men at least six hours per day.
- •7. If participant is unable to produce a spike of at least 6 mmHg from the base pressure on Biofeedback Pressure Unit and is unable to maintain the pressure created for 10 seconds.
排除标准
- •1. Individuals whose workstations have already been ergonomically altered for them.
- •2. Staff of bank other than bankers.
- •3. Neck Disability Index more than 28 points.
- •4. Individuals who are currently or were enrolled in a neck treatment programme for their neck pain within 12 months of the study's start date.
- •5. Individuals who have suffered any type of cervical surgery or trauma for example, in a vehicle accident or sports injury.
- •6. Previous experience of using a scapular or shoulder brace.
- •7. Individuals suffering from or who have previously suffered from cancer, any systemic illness process, skin sensitivity or infection.
- •8. Participants with particular pathologies e.g., congenital cervical anomalies stenosis, fracture, radiculopathy) or inflammatory diseases (e.g., rheumatoid arthritis.
- •9. Participants who expect to be absent from work for more than three days in a row throughout the research intervention period, as well as pregnant women.
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