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CTRI Number  CTRI/2024/06/068838 [Registered on: 13/06/2024] Trial Registered Prospectively
Last Modified On: 03/10/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Physiotherapy (Not Including YOGA)
Behavioral
Other (Specify) [mHealth]  
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Evaluation of mobile app-supported intervention for rehabilitation care after knee replacement 
Scientific Title of Study   Evaluation of mHealth supported intervention for rehabilitation monitoring after knee replacement – An open-label randomised controlled trial 
Trial Acronym  Not applicable 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Niveditha Devasenapathy 
Designation  Lead, Better Treatments 
Affiliation  The George Institute for Global Health INDIA 
Address  Room number 308,Third Floor, Research and Development, Elegance Tower Plot No. 8, Jasola District Centre

South
DELHI
110025
India 
Phone    
Fax    
Email  NDevasenapathy@georgeinstitute.org.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Niveditha Devasenapathy 
Designation  Lead, Better Treatments 
Affiliation  The George Institute for Global Health INDIA 
Address  308, Third Floor, Elegance Tower Plot No. 8, Jasola District Centre

South
DELHI
110025
India 
Phone  9810397722  
Fax    
Email  NDevasenapathy@georgeinstitute.org.in  
 
Details of Contact Person
Public Query
 
Name  Dr Niveditha Devasenapathy 
Designation  Lead, Better Treatments 
Affiliation  The George Institute for Global Health INDIA 
Address  308, Third Floor, Elegance Tower Plot No. 8, Jasola District Centre

South
DELHI
110025
India 
Phone  9810397722  
Fax    
Email  NDevasenapathy@georgeinstitute.org.in  
 
Source of Monetary or Material Support  
DBT/Wellcome Trust India Alliance, Nishant House, 8-2-351/N/1, 2nd floor, Road No. 2, Venkateshwara Hills, Banjara Hills, Hyderabad - 500034 
 
Primary Sponsor  
Name  The George Institute for Global Health India 
Address  08, Third Floor, Elegance Tower Plot No. 8, Jasola District Centre New Delhi 110025, India  
Type of Sponsor  Research institution 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 2  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Sahil Batra  All India Institute of Medical Sciences  Room Number 733, National Centre of Ageing, AIIMS, Ansari Nagar, New Delhi - 110029
New Delhi
DELHI 
01126551179

sahilbatra25@gmail.com 
Dr Prof Rajesh Malhotra  Indraprastha Apollo Hospital  Room number 1212, second floor, Apollo Hospital, Sarita Vihar, Delhi-Mathura Road, New Delhi-110076
South
DELHI 
91-11-71791212

rmalhotra62@yahoo.com 
 
Details of Ethics Committee  
No of Ethics Committees= 2  
Name of Committee  Approval Status 
INSTITUTE EHTICS COMMITTEE FOR BIOMEDICAL AND HEALTH RESEARCH  Approved 
INSTITUTIONAL ETHICS COMMITTEE - BIOMEDICAL RESEARCH  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: M170||Bilateral primary osteoarthritis of knee,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  TReAT App [TeleRehabilitation after knee ArThroplasty]   Intervention contains five components namely education material, videos of exercises, self-management tools using e-diary, monitoring, and consultation via a mobile application. Patients randomised to the intervention group will be provided with the mobile application and a manual to navigate through the app. Healthcare providers will also be able to use the app and monitor patients progress remotely. Routine clinic visits will continue as per usual practice. Physiotherapists will be able to modify patients treatment plan via the app, if required. The intervention will be available to patients for the duration of 6 months.  
Comparator Agent  Usual care  Patients randomized to usual care group will receive routine hospital care as per hospital norms.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  90.00 Year(s)
Gender  Both 
Details  1. Adult patients (aged ≥ 18 years) scheduled for primary partial or total (unilateral or bilateral) knee arthroplasty indicated for knee arthritis.
2. Patient has access to a smartphone and internet connection
3. Patient or any of the family members living in the same household is familiar with navigating a smartphone and able to use common features such as video calling, messaging, and camera
4. Patients able to speak and read English or Hindi language
 
 
ExclusionCriteria 
Details  1. Revision knee arthroplasty
2. Knee replacement indicated for trauma, tuberculosis of knee joint or other septic arthritis
3. Patients who are unable to make a hospital visit at 3 and 6 months after surgery
4. Patients who have severe cognitive impairment precluding ability to provide fully informed consent
5. Uncorrectable hearing and visual impairment
6. Not willing to be randomized to the rehabilitation approaches
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Centralized 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Patient reported knee function  3 and 6 months 
 
Secondary Outcome  
Outcome  TimePoints 
knee pain   3 and 6 months 
Knee range of motion  3 and 6 months 
Gait speed and stability  3 and 6 months 
Balance  3 and 6 months 
Lower limb strength  3 and 6 months 
Lower extremity activity level  3 and 6 months 
Safety (number of falls)  3 and 6 months 
Patient experience  6 months 
Cost effect and utility  3 months 
 
Target Sample Size   Total Sample Size="300"
Sample Size from India="300" 
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 3/ Phase 4 
Date of First Enrollment (India)   24/06/2024 
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="8"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
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
Modification(s)  

Monitoring of Physical rehabilitation is an essential component of patient recovery after knee arthroplasty. Monitoring can be remote or clinic-based. In India, unsupervised home-based physical rehabilitation is a common practice, and there is lack of evidence to demonstrate effectiveness of remote monitoring of rehabilitation. Therefore, we developed and piloted a mobile application [Tele REhabilitation after knee ArThroplasty (TReAT app)] based on behavior design-design thinking approach to support the recovery period. The TReAT app consists of five components: knowledge, skills, self-management & motivation, communication with healthcare providers, and monitoring by healthcare providers. We aim to compare the effectiveness, acceptability, cost, and safety of this app-based intervention against usual care (home-based with various levels of in-person supervision in clinic) using open label, 1:1 individual randomized superiority trial at two tertiary care hospitals in Delhi.

The primary objective would be to compare patient reported knee function between the two groups at 3- and 6-months post-surgery. Additionally, we will also compare patient reported outcomes (pain, falls), performance-based outcomes (lower limb strength and function), knowledge about recovery, rehabilitation adherence, satisfaction with surgery, resource utilization and cost, quality of life. End user experience and fidelity of the implementation will be measured using both quantitative and qualitative methods.

Consecutive adult patients undergoing partial or total (unilateral or bilateral) knee arthroplasty at each of the hospitals (one unit) will be screened for eligibility. Consenting individuals will be randomized to either app-supported intervention or usual care group. The target sample size is 300 patients, to be recruited over a period of one year. Data will be collected at baseline, 3 months, and 6 months post-surgery by a trained research coordinator. Anonymous quantitative data will be entered and stored in a web-based electronic data capture system. Qualitative data will be stored securely in password protected folders and data will be anonymized before analysis to maintain patient confidentiality. Quantitative data will be analysed in Stata17, and group comparisons will be done using mixed effect linear regression. Qualitative data will be analyzed via an inductive-deductive approach using NVivo software.

The trial is funded by DBT-Wellcome trust India alliance and trial will be initiated after obtaining ethical approvals from The George Institute for global health (Sponsor), India, All India Institute of Medical Sciences, Delhi and Indraprastha Apollo Hospital, Delhi. All ethical guidelines will be followed related to voluntary informed consent and data confidentiality laid by ICMR for conduct of research on human participants. The trial will be insured, and any trial related harm will be compensated. Participants will be provided monetary compensation for trial specific hospital visits as per institutional norms and ethical guidelines.

This intervention can be incorporated into routine clinical practice for remote supervision of home-based rehabilitation given it is proven to be clinically effective, safe, cost effective and accepted by the end users. This would serve the aim of improving patient experience and aid in faster recovery post knee arthroplasty.

 
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