Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06460662
Status:
COMPLETED
Last Update Posted:
2024-06-14
First Post:
2024-06-11
Brief Title:
Effects of Agility and Perturbation Based Training in Addition to Routine Physical Therapy
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Agility and Perturbation Based Training in Addition to Routine Physical Therapy on Pain Function and Quality of Life in Patients With Knee Osteoarthritis
Status:
COMPLETED
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Osteoarthritis is a degenerative joint disease Knee OA patients sometimes report episodes of knee instability that limit their ADLs The episodes of instability are similar to those reported in knee ligament injuries It is believed that modifications of interventions that are used to promote knee stability in knee ligament injuries can be used in knee OA to enhance knee stability and function The purpose of this study will be to determine the effects of agility and perturbation-based training in addition to routine physical therapy on pain function quality of life and disability in knee osteoarthritis
Detailed Description:
A Randomized Clinical Trial will be conducted at Al Syed Touqeer Altaf Surgical Hospital through a convenience sampling technique on 26 patients which will be allocated using computer-generated randomization into two groups Group A will be treated with agility and perturbation training techniques in addition to the same routine physical therapy as Group B and Group B will receive only routine physical therapy Outcome measures will be conducted through NPRS WOMAC SF-36 and KOS-ADLs questionnaires All the outcome measures will be assessed pre and post-treatment and the assessor will be blind Frequency of the treatment will be 3 sessions per week for 4 weeks Data will be analyzed using SPSS software version 25
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None