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Enrolling by invitation NCT06211387

ADDITIVE BENEFITS of KALTENBORN SUSTAINED STRETCH JOINT MOBILIZATION with RESISTANCE EXERCISE TRAINING in KNEE OSTEOARTHRITIS

No phase Interventional Knee Osteoarthritis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Resistance Exercise Training, Joint Mobilization.
Who it may be relevant to
Registry conditions: Knee Osteoarthritis. Basic parameters: 40 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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

Interventions

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

Primary outcome measures

  • Knee Pain [Time frame: 4 weeks]
  • Physical Function [Time frame: 4 weeks]
  • Isometric Muscle Strength [Time frame: 4 weeks]
  • Functional Mobility strength [Time frame: 4 weeks]
  • Cadence [Time frame: 4 weeks]
  • Gait velocity [Time frame: 4 weeks]
  • Stride length [Time frame: 4 weeks]
  • Knee range of motion (ROM) [Time frame: 4 weeks]

Eligibility criteria

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

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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Foundation University Islamabad — Islamabad

Identifiers

NCT: NCT06211387 · FUI/CTR/2023/22

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗