Instrumental Versus Standard Rehabilitation for Knee Osteoarthritis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-07-01

Study Completion Date

2024-12-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

A randomized clinical trial to evaluate the effectiveness of an instrumental rehabilitation protocol compared with standard protocol In patients with knee osteoarthritis.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Evaluation of the Efficiency of Propioceptive Study According to Radiological Stages in Patients With Knee Osteoarthritis

NCT06150170

Knee Osteoarthritis

COMPLETED NA

The Effect of Telerehabilitation-Based Exercise and Training on Outcome Measures in Patients With Knee Osteoarthritis

NCT05209893

Osteoarthritis Knee Arthritis

COMPLETED NA

Pain Function and QOL Undergoing Whole-Body Vibration and Exercise in End-Stage Knee Osteoarthritis

NCT06183177

Knee Osteoarthritis Pain, Joint

COMPLETED NA

Ultrasound-guided Radiofrequency Ablation of the Genicular Nerve Versus Physical Therapy for Chronic Knee Osteoarthritis

NCT06173830

Chronic Knee Osteoarthritis

RECRUITING NA

Strengthening Exercises Versus Proprioception and Balance Exercises in the Treatment of Knee Osteoarthritis

NCT03893981

Osteo Arthritis Knee Pain

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This is a randomized clinical trial designed to compare two intervention aimed at reducing and improving knee function in patients with knee osteoarthritis

\- sixty subjects suffering from knee osteoarthritis will be recruited; 30 per group.

A: instrumental rehabilitation B:standard rehabilitation All patients who meet the clinical inclusion and exclusion criteria will have a standard radiography

* selected patients will be invited to participate and will be informed of the purpose and conduct of the study
* patients will be randomized to either the instrumental rehabilitation programme groupe or the standard rehabilitation group
* patients in both groups will have a protocol that will be extended over 6 weeks
* participants will be assessed primarily for function and pain, as well as other secondary endpoints , at baseline at 3 weeks and at 12 weeks.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Knee Osteoarthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A randomized single blind clinical trial is a research study design used to evaluate the effectiveness of a medical intervention or treatment. In this type of trial, participants are randomly assigned to one of two a more groups, one groupe receives the experimental treatment, while the other group may receive a placebo or standard treatment, depending on the study's design

\- the term "single blind" refers to the fact that , in this trial the participants do not know whether they are receiving the experimental treatment or a control treatment this is done to minimize the potential for bias in reporting their symptoms or outcomes

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Masking is a technique used to keep treatment information indisclosed to the study participants while allowing researchers and treatment administration to know this information: study participants are not informed about the treatment they are receiving, they do not know whether they are receiving the experimental treatment under investigation or if they are in the control group , which may receive a placebo or standard treatment .

This helps reduce potential bias related to participant expectations

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

standard rehabilitation

rehabilitation of knee osteoarthritis patients using standard techniques of massage, stretching, muscle strengthening and balance work

Group Type ACTIVE_COMPARATOR

rehabilitation

Intervention Type OTHER

For the experimental group:

Isokinetic training Antigravity treadmill Posturography

For the control group:

Patients will receive a standard rehabilitation prescription comprising:

Physiotherapy , muscle stretching and strengthening , proprioceptive exercises, and self-programmed

instrumental rehabilitation

rehabilitation of knee osteoarthritis patients using isokinetic, posturograph and antigravity treadmill

Group Type EXPERIMENTAL

rehabilitation

Intervention Type OTHER

For the experimental group:

Isokinetic training Antigravity treadmill Posturography

For the control group:

Patients will receive a standard rehabilitation prescription comprising:

Physiotherapy , muscle stretching and strengthening , proprioceptive exercises, and self-programmed

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

rehabilitation

For the experimental group:

Isokinetic training Antigravity treadmill Posturography

For the control group:

Patients will receive a standard rehabilitation prescription comprising:

Physiotherapy , muscle stretching and strengthening , proprioceptive exercises, and self-programmed

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* patients with radiologically confirmed uni/ bilateral gonarthrosis

Exclusion Criteria

* Will be excluded from our study:
* Subjects with congestive gonarthrosis (joint effusion at clinical examination).
* Patients followed for chronic inflammatory rheumatism.
* Patients who are candidates for surgery for knee osteoarthritis
* Patients with a pathology causing a limitation in walking distance apart from gonarthrosis.
* Amputees of one or both lower limbs.

Eligible Sex

ALL

Accepts Healthy Volunteers

No