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临床试验/CTRI/2024/08/073160
CTRI/2024/08/073160已完成不适用

Immediate Effect of Craniosacral Therapy on Postpartum Neck Pain – an Experimental Study.

Self sponsored project1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2024年9月15日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
Numerical Pain Rating Scale (NPRS).

研究概览

简要总结

The study will involve obtaining ethical clearance, recruiting participants, collecting demographic data, and assessing postpartum women aged 21-40, hospitalized in the tertiary health care facility in Belagavi, Karnataka, will be randomly assigned to 2 clusters based on the presence or absence of neck pain symptoms. The cluster comprising women experiencing neck pain will receive craniosacral therapy, with assessments conducted before and after the therapy session. The participants will be asked to fill out the Numerical Pain Rating Scale (NPRS) and Neck Disability Index (NDI) questionnaires to measure their neck pain intensity and self-rated disability resulting from neck pain.  The Pressure Biofeedback Unit will be utilized as an objective measuring tool for assessing neck movement and strength of the cervical muscles. The scores and values from the NPRS, NDI questionnaires and Pressure Biofeedback Unit will be tabulated, analyzed, and interpreted to determine the intensity, weakness and resulting disability from postpartum neck pain. Following the completion of all outcome measures, the subject will then undergo Craniosacral therapy in a quiet, peaceful, and well-ventilated room for 30 minutes. During the session, the subject will be instructed to lie supine on the bed with the head resting on a pillow and arms comfortably resting on either side of the body. The therapist will be sitting at the head end of the subject and will gently place their hands on the cranium, sub-occipital region and shoulders of the patient to offer craniosacral therapy.   Following the craniosacral therapy, a follow-up assessment will be conducted 24 hours after the intervention. During this assessment, the Numerical Pain Rating Scale (NPRS), Neck Disability Index (NDI), and Pressure Biofeedback Unit measurements will be taken again. The data will then be tabulated, analyzed, and interpreted to assess any changes in the severity and disability resulting from postpartum neck pain.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
21.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • Postpartum women who are willing to participate.
  • Postpartum women suffering from neck pain.
  • Postpartum women between 21-40 years of age.

排除标准

  • Women with the history of chronic orthopaedic conditions.
  • Women suffering from febrile condition.

结局指标

主要结局

Numerical Pain Rating Scale (NPRS).

时间窗: Subjective pain assessment questionnaire to measure the pain intensity the patient feels

次要结局

  • Pressure Biofeedback Unit (Chattanooga)(Objective pain assessment questionnaire using the NPRS scale before the craniosacral treatment and 24 hours after the craniosacral therapy to measure any difference in pain intensity or severity.)

研究者

发起方
Self sponsored project
申办方类型
Other [Self sponsored project]
责任方
Principal Investigator
主要研究者

Dr Ashwini Bulbuli

KAHER institute of Physiotherapy

研究点 (1)

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