FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2026/02/104477 [Registered on: 23/02/2026] Trial Registered Prospectively
Last Modified On: 19/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Yoga & Naturopathy
Preventive
Behavioral 
Study Design  Single Arm Study 
Public Title of Study   The role of Bhramari Pranayam in reducing depression Among college going students 
Scientific Title of Study   Study the effect of Bhramari Pranayam for management of depression in college going students 
Trial Acronym  nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Prajwal Jivanrao Deshmukh 
Designation  PG Scholar 
Affiliation  BVDU College of Ayurved and Hospital 
Address  Bharati Vidyapeeth Deemed To Be University Department Of Kriya Sharira College Of Ayurved Dhankawadi Katraj Pune 411043

Pune
MAHARASHTRA
411043
India 
Phone  7448282252  
Fax    
Email  prajwaldeshmukhpd77@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Kavita Indapurkar 
Designation  Professor and HOD 
Affiliation  BVDU College of Ayurved and Hospital 
Address  Bharati Vidyapeeth Deemed To Be University Department Of Kriya Sharira College Of Ayurved Dhankawadi Katraj Pune 411043

Pune
MAHARASHTRA
411043
India 
Phone  9890791688  
Fax    
Email  kavita.indapurkar@bharatividyapeeth.edu  
 
Details of Contact Person
Public Query
 
Name  Dr Kavita Indapurkar 
Designation  Professor and HOD 
Affiliation  BVDU College of Ayurved and Hospital 
Address  Bharati Vidyapeeth Deemed To Be University Department Of Kriya Sharira College Of Ayurved Dhankawadi Katraj Pune 411043

Pune
MAHARASHTRA
411043
India 
Phone  9890791688  
Fax    
Email  kavita.indapurkar@bharatividyapeeth.edu  
 
Source of Monetary or Material Support  
Nil 
 
Primary Sponsor  
Name  Dr Prajwal Jivanrao Deshmukh 
Address  Sai Nagar lane no 3 samarth angan apartment 
Type of Sponsor  Other [self] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Prajwal Jivanrao Deshmukh  Bharati vidyapeeth college of ayurved pune  Bharati Vidyapeeth Deemed To Be University Department Of Kriya Sharira College Of Ayurved Dhankawadi Katraj Pune 411043
Pune
MAHARASHTRA 
7448282252

prajwaldeshmukhpd77@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics committee Bharati Vidyapeeth Deemed To Be University College Of Ayurved Pune  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  healthy participants 50(male/female) with age group 18 year to 24 year  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmProcedure-Bhramari Pranayam (Procedure Reference: Hathyog Pradipika, Procedure details: Sit in comfortable position with spine straight & shoulder relaxed close your eyes & take a few normal breaths place your index finger on the cartilage of your & gently press the ear flaps to block external sound alternatively you can place your thumb on the forehead & let your other fingers gently rest over the eyes & cheeks take a deep breath in through your nose filling your lungs completely with air as you exhale produce a humming sound similar to the buzzing of a bee the sound should come from throat not from mouth complete the exhalation & then inhale deeply again repeat 5 to 10 rounds per day for 12 weeks)
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  24.00 Year(s)
Gender  Both 
Details  College going students age group 18-24 years. Individuals of Either gender.
Individuals having HAM-D [Hamilton Depresssion Rating Scale] score less than 13 
 
ExclusionCriteria 
Details  Individuals suffering from any known major physical or psychological illness.
Individuals who are doing Pranayama regularly.
Individuals taking medication for psychological illness. 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
The study may reveal a change in the severity of depression as measured by the Hamilton Depression Rating Scale (HAM-D) score from baseline to 12 weeks after the Bhramari Pranayama intervention.  Depression will be monitored before and after yoga intervention during baseline 7th day 15th day 30th day 45th day 
 
Secondary Outcome  
Outcome  TimePoints 
Study may reveal change in HAM D score from baseline to 12 weeks  Depression will be monitored before & after yoga intervention at baseline duration of 7th day 15th day 30th day 45th day  
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   02/03/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  
Participants between the ages of 18 to 24 years were included in the study. They were informed about Bhramari Pranayama, including its procedure, as well as its potential positive and negative impacts. Informed consent was obtained from all participants prior to the initiation of the study.It was ensured that all participants had a score of less than 13 on the Hamilton Depression Rating Scale (HDRS), confirming eligibility for participation. Follow-up sessions have been scheduled at intervals of 7, 15, 30, and 45 days. Data will be collected during each follow-up, and the records will be maintained systematically.The collected data will be statistically analyzed and interpreted, and the final results will be presented accordingly.
 
Close