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Recruiting NCT06896032

Retro-walking Versus Forward-walking Training Using Underwater Treadmill in Patients With Knee Osteoarthritis

No phase Interventional Knee Osteoarthritis (Knee OA) 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: physical therapy intervention.
Who it may be relevant to
Registry conditions: Knee Osteoarthritis (Knee OA), Osteoarthritis. Basic parameters: 40 years — 60 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
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Retro-walking Versus Forward-walking Training Using Underwater Treadmill on Pain and Function in Patients With Knee Osteoarthritis

Overview

The purpose of this study Will investigate and compare the effects of retro-walking and forward-walking underwater treadmill training on pain, function and ROM in subjects with chronic knee OA

Detailed description

In the current study, Sixty subjects from both genders, the dominant side only will be involved. They will be divided in to three equal groups: group A (experimental1), group B (experimental 2), group C (control), they will be signed a consent form to share in this study which aimed to investigate the effects of retro-walking and forward-walking underwater treadmill training on pain, function and ROM in subjects with chronic knee OA

Interventions

  • Other physical therapy intervention
    retro-walking and forward-walking underwater treadmill training

Primary outcome measures

  • Pain intensity [Time frame: up to three monthes]
  • knee disability [Time frame: up to three months]
Secondary outcome measures (1)
  • knee range of motion [Time frame: up to three months]

Eligibility criteria

Inclusion criteria

  • 60 patients with chronic knee OA.
  • Age ranges from 40-60 years old of both genders.
  • body mass index (BMI) 25- 35kg/m2.
  • The degree of osteoarthritis was mild or moderate and have a Kellgren- Lawrence radiographic grade of of1-3.
  • unilateral knee osteoarthritis involvement.

Exclusion criteria

  • hydrophobia.
  • pregnancy.
  • infection.
  • psychiatric disorder.
  • haemorrhagic diathesis.
  • cardiac pacemaker.
  • all Subjects with deformity of hip, knee \& ankle.
  • any CNS or PNS involvement.
  • recent steroidal or intraarticular injections (3 months).
  • systemic inflammatory disease and bone malignancy.

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

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 2 centers
  • cairo U — Cairo
  • cairo U — Cairo

Identifiers

NCT: NCT06896032 · P.T.REC/012/005428

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗