Efficacy of Sub Occipital and Upper Trapezius Muscle Release on Various GI and Autonomic Parameters in Patients with Upper Cross Syndrome
试验速览
- 阶段
- 1/2 期
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- GSRS scale
研究概览
简要总结
It is a randomized controlled trial double blinded study with a duration of 4 weeks and involving 70 patients that will be divided into two groups by lottery method. Intervention for first group includes Myofascial release and hot pack, intervention for second group (Conventional group) is Neck Isometric exercises, TENS and hot pack. Firstly, the patients will be informed about the study, and informed consent will be taken from them. Before beginning the treatment each patients demographic data including age, gender, weight and height will be gathered as a baseline data. Pre-intervention measurements of outcome variables including Heart rate Variability, Tenderness Rating Scale, Gastrointestinal Symptom Rating Scale, Blood Pressure and Pulse Rate will be taken. Intervention will be given for 4 weeks and then the post-intervention data of all the outcome variables will be taken.
Recruitment, intervention, and data collection have been completed. A total of 70 participants were enrolled in the study. Data analysis is complete, and the thesis has been submitted in 1 July 2025. The manuscript has been prepared and is currently under review by the research supervisor prior to submission for publication.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- All
入选标准
- •Age group 20-40 year Both Males and females will be included in the study Neck pain from last 2-3 months Participants with trigger point in upper Trapezius muscle (criteria describe by Travell and simon) Participants with GIT symptoms (Heartburn,Flatulence ,Bloating etc) Participants willing to participate in the study.
排除标准
- •Participants with History of referred pain and surgery Participants with spinal degenerative joint disease Participants with motor vehicle accident ,trauma, fracture Participants with cardiovascular disorders Participants with neurological disorders Participants with endocrinal disorders Participants with psychological disorders Uncooperative participants.
结局指标
主要结局
GSRS scale
时间窗: The outcome measures will be assessed at baseline and after 4 weeks.
Tenderness rating scale
时间窗: The outcome measures will be assessed at baseline and after 4 weeks.
Heart rate variability
时间窗: The outcome measures will be assessed at baseline and after 4 weeks.
次要结局
- Blood Pressure(Pulse rate)
研究者
Mahima
Department of Physiotherapy Guru Jambheshwar University ofScience and Technology, Hisar