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Recruiting NCT07653841

Perturbation Based Balance Training Versus Progressive Neuromuscular Training as an Adjunct to Conventional Physiotherapy for Pain Reduction and Functional Improvement in Knee Osteoarthritis

No phase Interventional Knee Arthritis Osteoarthritis Knee Arthritis, 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: Perturbation-Based Balance Training, Progressive Neuromuscular Training.
Who it may be relevant to
Registry conditions: Knee Arthritis Osteoarthritis, Knee Arthritis, Osteoarthritis. Basic parameters: 40 years — 70 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

This is an RCT aims to explore Perturbation-Based Balance Training versus Progressive Neuromuscular Training as an Adjunct to Conventional Physiotherapy for Pain Reduction and Functional Improvement in Knee Osteoarthritis.

Interventions

  • Other Perturbation-Based Balance Training
    3 sessions/week 20-25 min (2 sets × 30 sec/activity) Starts with Low-Moderate (slow, predictable external perturbations) progress to Moderate-High (fast, unpredictable perturbations) 30-35 min (3 sets × 45-60 sec)
  • Other Progressive Neuromuscular Training
    3 sessions/week 20-25 min (2 sets × 10-12 reps) starts with Low-Moderate (RPE 9-11) then proceeds to Moderate (RPE 11-13)

Primary outcome measures

  • Pain & Functional Ability [Time frame: Baseline to Week 6]
Secondary outcome measures (3)
  • Functional Mobility [Time frame: Baseline to Week 6]
  • Muscle strength [Time frame: Baseline to week 6]
  • Balance [Time frame: Baseline to week 6]

Eligibility criteria

Inclusion criteria

Male and female, aged between 40-70 years Diagnosed with knee osteoarthritis Grades I-III based on the Kellgren-Lawrence classification Chronic knee pain for ≥3 months Ability to walk independently

Exclusion criteria

Grade IV osteoarthritis Previous knee surgery or joint replacement Rheumatoid arthritis or inflammatory joint disease Recent intra-articular injection (<6 months) Severe systemic illness, Neurological disorders and Vestibular disorders

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
  • Institute of Medical Rehabilitation (IMR) — Islamabad

Identifiers

NCT: NCT07653841 · IIUI/RERC/ADT/2026/05/259

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗