ADDITIVE BENEFITS OF KALTENBORN SUSTAINED STRETCH JOINT MOBILIZATION WITH RESISTANCE EXERCISE TRAINING IN KNEE OSTEOARTHRITIS

Knee Osteoarthritis Clinical Trial

Official title:

ADDITIVE BENEFITS OF KALTENBORN SUSTAINED STRETCH JOINT MOBILIZATION WITH RESISTANCE EXERCISE TRAINING IN KNEE OSTEOARTHRITIS

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT06211387
• Other study ID #: FUI/CTR/2023/22
• Status: Enrolling by invitation
• Phase: N/A
• Start date: January 20, 2024
• Est. completion date: August 2, 2024

Study information

• Verified date: January 2024
• Source: Foundation University Islamabad
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

to determine the supplementary effects of Kaltenborn sustained stretch mobilization when combined with resistance training in the management of knee osteoarthritis.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 42
• Est. completion date: August 2, 2024
• Est. primary completion date: August 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 65 Years

Eligibility

Inclusion Criteria:

Grade I-III knee OA Both male and female nee osteoarthritis for at least 3 months knee pain no more than 8/10 Exclusion Criteria: Malignancy Any additional Inflammatory disorders Infection Knee trauma lower limb fracture Lumbar radiculopathy or myelopathy knee surgery Intra-articular steroid therapy in the last 2 months Total knee replacement (TKR). Total hip replacement (THR). Any neurological disorder Any cardio-pulmonary complications Rheumatoid arthritis Septic arthritis Recent history of trauma Osteoporosis or osteomyelitis Grade IV osteoarthritis -

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Procedure:
• Resistance Exercise Training
Resistance Exercise Training for knee
• Joint Mobilization
Tibiofemoral and Patellofemoral Joint Mobilization

Locations

Country	Name	City	State
Pakistan	Foundation University Islamabad	Islamabad	Federal

Sponsors (1)

Lead Sponsor	Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Knee Pain	Knee Pain will be quantified using Numeric Pain Rating Scale (NPRS). NPRS is a 11 point scale form 0-10. Lower Score on NPRS signifies less pain, whereas higher score on NPRS signifies more pain.	4 weeks
Primary	Physical Function	To determine the physical function related to knee osteoarthritis Western Ontario and McMaster Universities Arthritis Index (WOMAC) will be used with a total of 24 items and a higher score on WOMAC signifies poor outcome.	4 weeks
Primary	Isometric Muscle Strength	Modified Sphygmomanometer will be used to measure isometric muscle strength of the muscles of the knee joint. A higher score signifies greater strength.	4 weeks
Primary	Functional Mobility strength	5 repetition sit to stand test will be used to determine functional mobility strength. Less time to complete the task signifies better outcome.	4 weeks
Primary	Cadence	Observational gait analysis will be used to determine cadence. A higher score signifies better outcome.	4 weeks
Primary	Gait velocity	Observational gait analysis will be used to determine cadence. A higher score signifies better outcome.	4 weeks
Primary	Stride length	Observational gait analysis will be used to determine cadence. A higher score signifies better outcome.	4 weeks
Primary	Knee range of motion (ROM)	Gonimeter will be used to measure knee range of motion.. A higher score signifies better outcome.	4 weeks