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CTRI Number  CTRI/2026/03/105919 [Registered on: 11/03/2026] Trial Registered Prospectively
Last Modified On: 11/03/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Physiotherapy (Not Including YOGA) 
Study Design  Other 
Public Title of Study   To study the male and female postural alterations with heel raise on knee felxion, lumbar lordosis, pelvic incliation postural sway and line of gravity. 
Scientific Title of Study   TO STUDY THE MALE AND FEMALE POSTURAL ALTERATIONS WITH HEEL RAISE ON KNEE FLEXION, LUMBAR LORDOSIS, PELVIC INCLINATION, POSTURAL SWAY, AND LINE OF GRAVITY 
Trial Acronym  nil 
Secondary IDs if Any  
Secondary ID  Identifier 
rambophysio@rediffmail.com  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  JANWI DUGGAL 
Designation  PG STUDENT  
Affiliation  DAV Institute Of Physiotherapy And Rehabilitation  
Address  DAV Institute Of Physiotherapy And Rehabilitation, Mahatma Hansraj Marg, Opposite Burlton Park, Gurudev Nagar, Ram Nagar Jalandhar

Jalandhar
PUNJAB
144008
India 
Phone  6283824279  
Fax    
Email  duggaljanvi7@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  DR. JANWI DUGGAL 
Designation  PG STUDENT  
Affiliation  DAV Institute Of Physiotherapy And Rehabilitation  
Address  DAV Institute Of Physiotherapy And Rehabilitation, Mahatma Hansraj Marg, Opposite Burlton Park, Gurudev Nagar, Ram Nagar Jalandhar

Jalandhar
PUNJAB
144008
India 
Phone  6283824279  
Fax    
Email  duggaljanvi7@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr. Ram Babu(PT) 
Designation  Associate Professor 
Affiliation  DAV Institute Of Physiotherapy And Rehabilitation  
Address  DAV Institute Of Physiotherapy And Rehabilitation, Mahatma Hansraj Marg, Opposite Burlton Park, Gurudev Nagar, Ram Nagar Jalandhar

Jalandhar
PUNJAB
144008
India 
Phone  8284886611  
Fax    
Email  duggaljanvi7@gmail.com  
 
Source of Monetary or Material Support  
DAV Institute of Physiotherapy and Reahbilitation  
 
Primary Sponsor  
Name  Janwi Duggal  
Address  Dav Institute Of Physiotherapy And Rehabilitation  
Type of Sponsor  Other [] 
 
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 Janwi Duggal  DAV Istitute Of Physiotherapy And Rehabilitation  DAV.Institute of Physiotherapy and Rehablitation,Mahatma Hans Raj Marg, Opposite Burlton Park, Gurdev Nagar, Ram Nagar, Jalandhar, Punjab 144008
Jalandhar
PUNJAB 
06283824279

duggaljanvi7@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  normal healthy indiviual provided with heel raise as intervention for half an hour ehich wiol act as adaptive mechanism, data will be recorded pre adaptive and post adapative  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Heel raise  A modified footwear with a Heel raise of 6.6cm is inlcuded in the study for male subjects where as female subjects will be asked to bring their own foot wear with heel raise 6.6cm to observe the postural adaptation  
Comparator Agent  NOT APPLICABLE   NOT APPLICABLE  
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  39.00 Year(s)
Gender  Both 
Details  Subjects of both genders (male and female) will be included.
Subjects between 20 and 39 (young adults) years of age
Normal healthy individuals will be included with BMI of 18.5-24.9kg/m2
Subjects who will give written consent
Females with their own footwear with heel height of 6.6cm using for 2 days a week from past 6 months will be included.
 
 
ExclusionCriteria 
Details  Subjects who have previous surgery or injury of 6 months related to ankle, knee, pelvic, and lumbar.
Subjects with any pain during the time of data collection.
Subjects with any experimental site skin infections, allergic reactions or lesions.
Subjects with any neurological condition which making them difficult to stand still.
Subjects with involvement of any motor and sensory impairment.
Deformity in foot, knee and hip.
Subjects with radiculopathy to the lower limb.
Pregnant woman
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Participant and Investigator Blinded 
Primary Outcome  
Outcome  TimePoints 
change in the angle of knee flexion
change in the angle of lumbar lordosis
change in the angle of pelvic inclination
change in the Line of gravity
chnage in the postural sway  
pre intervention and post intervention 
 
Secondary Outcome  
Outcome  TimePoints 
NIL  NIL 
 
Target Sample Size   Total Sample Size="55"
Sample Size from India="55" 
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   N/A 
Date of First Enrollment (India)   22/03/2026 
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="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
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  

The total duration  of study is 1.5 years . The male and female subjects with in age of 20-39 years will be included. The subjects wgho fulfil the inclusiona and exclusion criteria will be incuded.  The study will be conducted in a controlled laboratory. Postural parameters including knee flexion angle, lumbar lordosis, and pelvic inclination will be assessed in the sagittal plane using digital photographic analysis. Reflective markers will be placed over standardized anatomical landmarks (ASIS, PSIS, greater trochanter, lateral femoral epicondyle, and lateral malleolus). Photographs will be captured using a smartphone mounted on a tripod positioned 180 cm from the participant at a height of 100 cm. Participants will stand barefoot in a habitual standing posture while maintaining gaze on a fixed point on the wall. Five images will be obtained and analyzed using Kinovea software. Then the paitents will be asked to stand on a force plate for postural sway. After barefoot measurements, the male participants will be provided with heel raise of 6.6cm foot wear where as female will be asked to wear there own . Then they undergo a 30-minute acclimatization period with heel raise footwear. The same measurement procedure will then be repeated. Two independent evaluators will analyze the images, and the average values will be used for statistical analysis.

 
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