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CTRI Number  CTRI/2026/02/103496 [Registered on: 10/02/2026] Trial Registered Prospectively
Last Modified On: 10/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Other (Specify) [Physiotherapy]  
Study Design  Non-randomized, Active Controlled Trial 
Public Title of Study   Online Physiotherapy Treatment for Plantar Fasciitis. 
Scientific Title of Study   Effect of Telerehabilitation in Patients with Plantar Fasciitis. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Swati Sharma 
Designation  Student 
Affiliation  Sharda University 
Address  OPD-2, Department of Physiotherapy, F Block Sharda University plot no 32, 34 Knowledge park-3, Greater Noida, Uttar Pradesh 201310

Gautam Buddha Nagar
UTTAR PRADESH
201310
India 
Phone  9711108232  
Fax    
Email  2024338344.swati@pg.sharda.ac.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Kriti Sachan PT 
Designation  Assistant Professor, Department of Physiotherapy, Sharda University 
Affiliation  Sharda University 
Address  OPD-2, Department of Physiotherapy, F Block, Sharda University plot no 32, 34 Knowledge park-3, Greater Noida, Uttar Pradesh 201310

Gautam Buddha Nagar
UTTAR PRADESH
201310
India 
Phone  7251006215  
Fax    
Email  kriti.sachan@sharda.ac.in  
 
Details of Contact Person
Public Query
 
Name  Dr Kriti Sachan PT 
Designation  Assistant Professor, Department of Physiotherapy, Sharda University 
Affiliation  Sharda University 
Address  OPD-2, Department of Physiotherapy, F Block, Sharda University plot no 32, 34 Knowledge park-3, Greater Noida, Uttar Pradesh 201310


UTTAR PRADESH
201310
India 
Phone  7251006215  
Fax    
Email  kriti.sachan@sharda.ac.in  
 
Source of Monetary or Material Support  
Department of Physiotherapy, Sharda Hospital 
 
Primary Sponsor  
Name  Sharda university 
Address  Department of Physiotherapy, Sharda School of Allied Health Sciences, Sharda University, Greater Noida, Uttar Pradesh, India,201310 
Type of Sponsor  Other [Physiotherapy] 
 
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 Kriti Sachan PT  Sharda Hospital.  OPD-2, Department of Physiotherapy, F Block, Sharda Hospital, Greater Noida Plot no. 32, 34, Knowledge Park-3, Greater Noida, Uttar Pradesh 201310
Gautam Buddha Nagar
UTTAR PRADESH 
7251006215

kriti.sachan@sharda.ac.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Dr. Moumita Bala  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Plantar Fasciitis 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Group A (Telerehabilitation Group)  The patient will receive intervention through video call for 5 days per week for 8 weeks. 
Comparator Agent  Group B (Hospital Based rehabilitation Group)  The patient will receive intervention in the hospital for 5 days per weeks for 8 weeks. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  Patients with Plantar Fasciitis.
Age between 18 and older and able to use a mobile device.
Both male and female.
Patients experiencing heel pain and pain during the first few steps in the morning.
Patients willing to participate in a Tele- rehabilitation program.
 
 
ExclusionCriteria 
Details  Patients having foot or ankle fracture in the last three months.
Any neoplastic formation in the foot- ankle region.
Previous surgery to distal tibia, fibula, ankle joint or rear foot region.
Any systemic condition like severe rheumatoid arthritis, osteoarthritis.
Having serious pathologies like diabetes mellitus, severe heart and neuropsychiatric disorders.
Radiological evidence showing calcaneal spur.
Before randomization, have already undergone a physiotherapy or local injection.
 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Other 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
INDEPENDENT VARIABLES

Stretching exercises
Towel Stretch
Stretching of Calf
Plantar Fascia Self Stretching

Strengthening exercises with TheraBand

Self- Myofascial Release using a ball
 
8 weeks
 
 
Secondary Outcome  
Outcome  TimePoints 
DEPENDENT VARIABLES
Numeric Pain Rating Scale (NPRS) – For Pain
Foot Function Index (FFI) – For Functional Disability
SF- 36 Questionnaire – For Quality of Life
 
8 weeks 
 
Target Sample Size   Total Sample Size="68"
Sample Size from India="68" 
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)   03/03/2026 
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  
Patients will receive informed consent before beginning of the study. Patients will be provided with detailed explanation about safety procedures and purpose of the study including signs, symptoms and possible outcomes. Patient’s voluntary participation will be appreciated and participants can leave the study anytime without consequences.
Patients will be selected on the basis of selection criteria.
Patients will be randomly divided (chit method) into two groups-
Group A (Telerehabilitation Group)
Group B (Hospital Based rehabilitation Group)
Pre intervention data for both the groups (Group A and Group B) will be recorded for pain intensity, functional disability and Quality of life by using the Numeric Pain Rating Scale (NPRS), Foot Function Index (FFI) and SF-36 Questionnaire.

Group A - Patients in the Telerehabilitation Group will receive intervention through video call for 5 days per week for 8 weeks. The Exercises include are Towel Stretch, Stretching of Calf, Plantar Fascia Self Stretching, Strengthening with TheraBand of Ankle Plantar flexors, Ankle Dorsiflexors, Ankle Invertors and Ankle Evertors, Toe Curl with Towel, Self Myofascial Release using a ball.

Group B - Patients in the Hospital Based rehabilitation Group will receive intervention in the hospital for 5 days per week for 8 weeks. The Exercises include are Towel Stretch, Stretching of Calf, Plantar Fascia Self
Stretching, Strengthening with TheraBand of Ankle Plantar flexors, Ankle Dorsiflexors, Ankle Invertors and Ankle Evertors, Toe Curl with Towel, Self Myofascial Release using a ball.

After 8 weeks, Post intervention data from both the groups (Group A and Group B) will be recorded for pain intensity, functional disability and Quality of Life by using the Numeric pain Rating scale (NPRS), Foot Function Index (FFI) and SF-36 Questionnaire.

Pre and Post intervention data from both the groups (Group A and Group B) will be collected, evaluated and analyzed.


 
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