A clinical trial to study the efficacy of selected types of Pranayama in Anxiety Neurosis of working women.

Phase 3

Recruiting

• Conditions: Other specified anxiety disorders. Ayurveda Condition: RASAVAHASROTODUSHTIH, (2) ICD-10 Condition: F418||Other specified anxiety disorders. Ayurveda Condition: Manovahastrotasdushti,

• Registration Number: CTRI/2022/03/041300
• Lead Sponsor: Dr Mrunal Ashay Jamdade

Brief Summary

This study is randomized controlled trial to study the efficacy of selected Kumbhak Kriya - Pranayama in Anxiety Neurosis of working women. In this study pranayama are selected from Kumbhak Paddhati book which is written by Aacharya Raghuvira. There are two groups- Experimental and Control. Patients from experimental group will do Pranayama practices. Pranayama will be practiced by patients for 6 weeks and follow up will be taken on 7th, 21st, 42nd day. Observations will be recorded as per criteria of assessment. Appropriate statistical tests will be applied to data generated through clinical trial to reach to conclusion.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-03-30
• Last Update Posted: 2022-04-04

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

1.Voluntarily participating in the study 2.Understanding the study completely and signed Informed Consent Form 3.Married women 4.Working women 5.Free of any other major systemic disorders Ready to do pranayama study and diagnosed with Anxiety Neurosis.

Exclusion Criteria

1.Refusal to participation by patient 2.Unmarried women 3.Pregnant women 4.Non working women 5.Women having age less than 25 years and more than 45 years Having major systemic disorders other than Anxiety Neurosis.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary parameters to be assessed as follows with the help of Hamilton Anxiety rating scale	At baseline | 7th day | 21st day | 42nd day
1.Anxious mood	At baseline | 7th day | 21st day | 42nd day
2.Depressed mood	At baseline | 7th day | 21st day | 42nd day
3.Nausea	At baseline | 7th day | 21st day | 42nd day
4.Behaviour at interview	At baseline | 7th day | 21st day | 42nd day

Secondary Outcome Measures

Name	Time	Method
Parameters to be assessed with the help of Hamilton anxiety rating scale.	1.Insomnia

Trial Locations

Locations (1)

D Y Patil Ayurvedic Hospital, Special OPD; 🇮🇳 Thane, MAHARASHTRA, India

D Y Patil Ayurvedic Hospital, Special OPD

🇮🇳Thane, MAHARASHTRA, India

Dr Mrunal Ashay Jamdade

Principal investigator

8691923339

dr.mrunaljamdade@gmail.com