Osteo Arthritis Knee Clinical Trial
— CKOAIOfficial title:
Comprehensive Knee Osteoarthritis Index (CKOAI): Scale Development, Validation and Reliability Testing
Verified date | March 2019 |
Source | Maharishi Markendeswar University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background:
Symptoms, balance, mobility, activities of daily life (ADL) and quality of life (QoL) are to
be considered in rehabilitation of the individuals with knee osteoarthritis (IKOA). There are
several scales to evaluate subjective perceptions and individual components in patients with
osteoarthritis (OA). Till date, no scale is available to measure the combined balance,
mobility, ADL and QoL in PKOA.
Objectives:
The objectives of the study are to develop a combined measure of symptoms, balance, mobility,
ADL and QoL in PKOA, as comprehensive knee osteoarthritis index (CKOAI) and to validate the
scale for its content, reliability and minimum detectable change (MDC)
Methods:
The study consists of a three stages. First stage is the scale (CKOI) item development and
validation. This includes domain and item generating through systematic literature search to
extract items related symptoms, balance, mobility, ADL and QoL in IKOA based on the
International Classification of Functioning, Disability and Health (ICF) and through
structured interviews. During scale validation, an expert panel will review the generated
domains and items by Delphi Method, which will undergo revision and pilot testing. Based on
the responsiveness of pilot testing will be revised finally. Second stage is to test re-test
reliability. The third stage is to report the standard error of measurement (SEM) and minimal
detectable change (MDC).
Data analysis:
All the domains and items in CKOAI will undergo reliability and criterion-related validity.
Minimum 50 IKOA will be evaluated with the scale on two occasions within two weeks to
establish test retest reliability. Cronbach's alpha for internal consistency and Intra class
correlation coefficient for test retest reliability will be used to determine the degree of
consistency of items in the scale. MDC will be calculated using the formulae, SEM = SD x √
(1-reliability) and MDC95 = √2 x (1.9) x (SEM). Significant level will be set at p value less
than 0.05 (p < 0.05) to minimize the type-I error.
Status | Completed |
Enrollment | 52 |
Est. completion date | February 13, 2019 |
Est. primary completion date | February 12, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Individuals with osteoarthritic changes of grade 1 and greater on knee radiograph (Kellgren and Lawrence) - Individuals with unilateral or bilateral knee osteoarthritis - Both male and female - Individuals who able to understand simple command - Individuals who are willing to participate Exclusion Criteria: - History of hip and knee replacement surgery - History of knee arthroscopic surgery within 6 months - Any neurologic and musculoskeletal condition which affect their movement or balance - Comorbidities such as cancer or cardiovascular disease |
Country | Name | City | State |
---|---|---|---|
India | Maharishi Markandeshwar Institute of physiotherapy and Rehabilitation | Ambala | Haryana |
Lead Sponsor | Collaborator |
---|---|
Maharishi Markendeswar University |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Comprehensive Knee Osteoarthritis Index | Set of patient reported outcome measures | two occasions within two weeks to establish test retest reliability |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT04040985 -
Legion Primary Safety and Efficacy
|
N/A | |
Active, not recruiting |
NCT04525950 -
Robotized Navigation Compared to Conventional Technique in Total Knee Replacement
|
N/A | |
Recruiting |
NCT04320914 -
High Intensity Laser Therapy (Classes IV) and Ibuprofen Gel Phonophoresis for Treating Knee Osteoarthritis
|
N/A | |
Completed |
NCT03886142 -
Platelet Rich Plasma Versus Radio Frequency for Chronic Knee Arthritis
|
N/A | |
Terminated |
NCT04072055 -
MOTO Post-marketing Surveillance Study
|
||
Not yet recruiting |
NCT06385275 -
The Role of Vitamin K on Knee Osteoarthritis Outcomes
|
Phase 1/Phase 2 | |
Not yet recruiting |
NCT05290818 -
Total Versus Robotic Assisted Unicompartmental Knee Replacement
|
N/A | |
Withdrawn |
NCT03271229 -
Conventional Platelet-Rich Plasma Versus Concentrated Bone Marrow Stem Cell Injections for Osteoarthritis of the Knee
|
Phase 2 | |
Recruiting |
NCT05992038 -
Use of a Putty as Gap Filler in Open-wedge Osteotomy
|
N/A | |
Recruiting |
NCT05505552 -
Effects of Vitamin K on Lower-extremity Function in Adults With Osteoarthritis:
|
N/A | |
Recruiting |
NCT06066684 -
Pain Phenotyping in Knee OA: a Pilot Trial
|
||
Completed |
NCT03847324 -
Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty
|
N/A | |
Recruiting |
NCT05126485 -
Biofeedback Retention in Individuals With AKA
|
Early Phase 1 | |
Completed |
NCT04956393 -
The SOAR (Stop OsteoARthritis) Program Proof-of-Concept Study
|
N/A | |
Recruiting |
NCT04541342 -
Arthroscopic Evaluation of Cartilage Regeneration After Opening-wedge High Tibial Osteotomy
|
N/A | |
Completed |
NCT04391842 -
Sustained Acoustic Medicine (SAM) Combined With a Diclofenac Ultrasound Coupling Patch for Knee Osteoarthritis
|
Phase 1 | |
Completed |
NCT03680807 -
Power Production in Older Adults With Knee Osteoarthritis
|
||
Completed |
NCT03783455 -
Effectiveness of Five Intraarticular Strategies on Knee Osteoarthritis
|
N/A | |
Not yet recruiting |
NCT06264362 -
Developing a Nonpharmacological Pain Intervention for Community-dwelling Older Adults With Dementia
|
N/A | |
Completed |
NCT05089253 -
Effect of Physical Therapy Modalities in Osteoarthritis
|
N/A |