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CTRI Number  CTRI/2025/12/099855 [Registered on: 26/12/2025] Trial Registered Prospectively
Last Modified On: 24/12/2025
Post Graduate Thesis  No 
Type of Trial  Observational 
Type of Study   Cross Sectional Study 
Study Design  Other 
Public Title of Study   Study to see how Knee pain can limit Activities of Daily Living 
Scientific Title of Study   Pain and Body Function Limitations in Primary Knee Osteoarthritis: A Cross-sectional study on International Classification of Functioning, Disability and Health based Assessment 
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. Satyasheel Singh Asthana 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences, Raebareli 
Address  Room 28, Department of Physical Medicine and Rehabilitation, All India Institute of Medical Sciences, Raebareli, Dalmau Rd, Uttar Pradesh 229405

Rae Bareli
UTTAR PRADESH
229405
India 
Phone  9169385726  
Fax    
Email  satyapmr2015@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Satyasheel Singh Asthana 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences, Raebareli 
Address  Room 28, Dept. of Physical Medicine and Rehabilitation, All India Institute of Medical Sciences, Raebareli, Dalmau Rd, Uttar Pradesh 229405

Rae Bareli
UTTAR PRADESH
229405
India 
Phone  9169385726  
Fax    
Email  satyapmr2015@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Satyasheel Singh Asthana 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences, Raebareli 
Address  Room 28, Department of Physical Medicine and Rehabilitation, All India Institute of Medical Sciences, Raebareli, Dalmau Rd, Uttar Pradesh 229405

Rae Bareli
UTTAR PRADESH
229405
India 
Phone  9169385726  
Fax    
Email  satyapmr2015@gmail.com  
 
Source of Monetary or Material Support  
NIL 
 
Primary Sponsor  
Name  All India Institute of Medical Sciences, Raebareli, Uttar Pradesh  
Address  All India Institute of Medical Sciences, Raebareli, Dalmau Rd, Munshiganj, Madhupuri, Uttar Pradesh 229405  
Type of Sponsor  Government medical college 
 
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 Satyasheel Singh Asthana  All India Institute of Medical Sciences, Raebareli   Room 22/28, Ground floor, Department of Physical Medicine and Rehabilitation, All India Institute of Medical Sciences, Raebareli, Dalmau Rd, Munshiganj, Madhupuri, Uttar Pradesh 229405
Rae Bareli
UTTAR PRADESH 
9169385726

satyapmr2015@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee (IEC), AIIMS Raebareli   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: M179||Osteoarthritis of knee, unspecified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Nil  Nil 
 
Inclusion Criteria  
Age From  50.00 Year(s)
Age To  90.00 Year(s)
Gender  Both 
Details  Age more than fifty years
Symptoms of primary osteoarthritis knee with radiological evidence of OA knee
 
 
ExclusionCriteria 
Details  Post-traumatic or post-operative knees
Neurological or rheumatologic comorbidities
Neuromuscular Disorders
Cognitive impairment
Refusal of consent to take part in study
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Numerical Pain rating Scale (NPRS)
Body Functions in ICF Core Set for Osteoarthritis (Comprehensive)
 
Baseline only. No Follow up. 
 
Secondary Outcome  
Outcome  TimePoints 
Western Ontario & McMaster Universities Osteoarthritis Index (WOMAC) Scale  Baseline only. No Follow ups 
 
Target Sample Size   Total Sample Size="239"
Sample Size from India="239" 
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)   05/01/2026 
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="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
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  

Background

The impact of knee Osteoarthritis (OA) on Quality of life (QoL) is profound. Individuals with knee OA often experience chronic joint pain, morning stiffness, and progressive difficulty in performing basic tasks such as walking, climbing stairs, and squatting. These limitations not only hinder physical mobility but also affect emotional well-being, social participation, and independence. Studies have shown that the severity of knee pain and functional disability are directly associated with lower scores on health-related QoL assessments, such as the Short Form-36.

The association between pain and function in knee OA is well-documented, integrating this relationship using the ICF framework offers a more holistic understanding. This approach may help bridge gaps in clinical assessment and promote individualized care strategies tailored to the specific functional challenges experienced by OA patients.

By using the ICF framework, the study will likely reveal how pain intensity affects not just mobility but also broader aspects of daily living and participation. It is anticipated that individuals reporting higher Numeric Pain Rating Scale (NPRS) scores will also show more limitations in ICF activity domains such as walking, stair-climbing, self-care, and social participation. The study will also provide ICF-based functional profiles that can help classify patients based on pain-disability patterns.

Primary Objective

To assess the relationship between pain intensity and body function limitations in individuals with knee osteoarthritis using the International Classification of Functioning, Disability and Health (ICF) framework.

Secondary Objective

To examine the association between radiographic severity (Kellgren-Lawrence grade), Pain and functional limitations (WOMAC).

Methodology

Type of study Cross-sectional Study

Duration of Study Two years

Study Population Patients of Primary Osteoarthritis Knee

Total Sample Size= Two hundred thirty nine

Inclusion Criteria

Age  more than fifty years

Symptoms of primary osteoarthritis knee with radiological evidence of OA knee

 

Exclusion Criteria

Post-traumatic or post-operative knees

Neurological or rheumatologic comorbidities

Neuromuscular Disorders

Cognitive impairment

Refusal of consent to take part in study

Sampling Technique

Consecutive sampling will be employed to select study participants from patients attending the Outpatient Department (OPD) or In-patient Department (IPD) of Physical Medicine and Rehabilitation.

Study Plan

Patient will be recruited from department of Physical Medicine and Rehabilitation OPD/IPD. Study will be started only after getting approval from Institutional Ethical Committee. Patients will be evaluated for inclusion and exclusion criteria. Written and informed consent will be taken from all participants. All the data will be recorded in working proforma Patients will be evaluated using 3 Scales/questionnaires: Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) for functional assessment. Pain will be assessed using Numeric Pain Rating Scale (NPRS). Body Functions in ICF Core Set for Osteoarthritis (Comprehensive) for assessment of body functions.

Scales/Questionnaires

Numerical Pain rating Scale (NPRS): It is a commonly used, simple, and effective tool for assessing the intensity of pain experienced by an individual. Patients are asked to rate their pain intensity by selecting a number between 0 (no pain) and 10 that best describes their current pain experience. The scale is typically presented visually (on a line or as a series of numbers) or verbally, depending on the clinical context. The scale is valid, reliable and has internal consistency of 0.87.

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Scale: It is a widely validated, disease-specific instrument used to evaluate pain, stiffness, and functional limitation in individuals with knee and hip osteoarthritis (OA). It comprises 24 items divided into three subscales- pain (5 items), stiffness (2 items), and physical function (17 items). The WOMAC can be administered using Likert, Visual Analog Scale (VAS), or Numerical Rating Scale (NRS) formats, with higher scores indicating worse symptoms. WOMAC has demonstrated excellent psychometric properties in knee OA populations. The internal consistency is high, with Cronbach’s alpha ranging from 0.86 to 0.96 for its subscales, and test-retest reliability coefficients exceeding 0.80, confirming its stability over time. It has strong construct and content validity, with responsiveness to clinical changes, making it a preferred outcome measure in OA research and rehabilitation settings.

Body Functions in ICF Core Set for Osteoarthritis (Comprehensive): It is a standardized tool based on the WHO’s International Classification of Functioning, Disability and Health (ICF) framework. It includes key categories across body functions, activities, participation, and environmental factors relevant to individuals with osteoarthritis. This tool enables a comprehensive assessment of how OA affects daily life and social functioning. It has demonstrated strong content and construct validity, and studies show moderate to high inter-rater reliability when used by trained professionals. The brief format makes it suitable for clinical and research settings, supporting a holistic, patient-centered approach to OA assessment. It covers three major domains: Body Functions, Activities and Participation, and Environmental Factors. Body Function has 13 body function assessment, scores from 0 to 4, not specified and not applicable.

Statistical Analysis

Descriptive statistics will be used to summarize demographic variables and responses from the ICF Core Set for Osteoarthritis (Brief), including measures such as frequency, percentage, mean, and standard deviation as appropriate. To examine associations between categorical variables, the Chi-square test will be applied. ICF responses with not specified and not applicable will be not included in ICF based stats analysis. Correlation between pain intensity and body function limitations, will be analyzed using correlation analysis, either Pearson’s or Spearman’s correlation coefficient, depending on the distribution of the data. To identify whether pain levels can predict the degree of body function limitation, a regression analysis will be performed. For all statistical tests, a p-value of less than 0.05 will be considered statistically significant. All data will be analyzed using IBM SPSS Statistics software, version 29.

 

 

 

 
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