Effectiveness of Integrated Yoga (selected Yoga Postures, Pranayama, & Relaxation technique for reducing pain, stiffness mental discomfort & enhancing the movement of the neck in patients of Cervical spondylosis

Phase 4

Not yet recruiting

• Conditions: Spondylosis, unspecified. Ayurveda Condition: GRIVASTAMBAH/GRIVAHUNDANAMÂ (KEVALAVATA),

• Registration Number: CTRI/2023/07/055834
• Lead Sponsor: UGC Non Net Fellowship BHU

Brief Summary

The purpose of the study is to evaluate the effectiveness of specificshukshma vyayam Yoga postures pranayama relaxation techniques andmedication in cases of cervical spondylosis that have been medically diagnosed For the control and study groups a total of 150 cases can be collected Well administerAyurvedic medications to the control group Based on the questionnaires viz the Visual Analog Scale VAS Neck Disability Index NDI and DepressionAnxiety Stress Scale DASS were used to measure the Neck Disability cervicalspondylosis and associated discomfort And three groups will becontrasted for improvement in pain stiffness and neck movements after 15 30 45 and 60 days All Yoga interventions and test variables are non intrusive Still written informed consent will be obtained

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-07-27
• Study Start: 2023-08-08

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

• 1. In this study, the subject’s ages ranging from 20-60 years were selected. 2. Either sex suffering from cervical pain, disability, and mental discomfort will be registered for the study. 3. Mild and moderate cases of cervical Spondylosis will be considered. 4. Only 150 subjects were selected for this study. 5.
• In this study Ayurvedic preparation, Manasamitra vataka, Manasamitra vataka, Vatavidhvamsana rasa, and Panchagavya Ghrita were administered to Cervical Spondylosis persons.

Exclusion Criteria

• The age category of male/female/transgender would be below 20 and above 60.
• Patients who have any major surgery especially heart, brain, etc.
• Patients who have previous medical history of hormonal contraceptives.
• Pregnant women will not be considered in this study.
• Severe cases of cervical spondylosis will not be considered.
• Patients sufferings from Diabetes mellitus, renal failure, Paralysis, Parkinson’s disease, severe Anaemia, Malignancy, Leprosy, Bleeding disorder, and other severe diseases shall be excluded from research work.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
VAS(Visual Analog Scale)	18 months
NDI(Neck Disability Index)	18 months
DASS(Depression Anxiety Stress scale)	18 months

Secondary Outcome Measures

Name	Time	Method
DASS(Depression Anxiety Scale)

Trial Locations

Locations (1)

S S Hospital IMS BHU; 🇮🇳 Varanasi, UTTAR PRADESH, India

S S Hospital IMS BHU

🇮🇳Varanasi, UTTAR PRADESH, India

Rohit Kumar

Principal investigator

8127973433

rohit812797@bhu.ac.in