Knee Osteoarthritis Clinical Trial
Official title:
Exercise Therapy in Patients With Knee Osteoarthritis
Osteoarthritis (OA) is one of the most common form of chronic diseases in the adult
population, and approximately 800 000 people in Sweden (population of 9 million people)
suffer from this disease, which causes joint pain, stiffness, swelling, loss of function and
sick leave. There is increasing evidence that exercise therapy is effective for patients with
knee OA. However, there is little knowledge on long-term effects and what type of exercises
dosage is most effective. In this present clinical trial, which is a Nordic collaborative
project with researchers from different research groups in Sweden and Norway, we intend to
investigate short and long-term effects comparing high dosage exercise therapy (each
treatment lasting 80 to 90 min) vs. a relatively low dosage exercise program (25 to 30 min)
in patients diagnosed with knee OA. Patients in both intervention groups receive three
treatments a week for 12 weeks making a total of 36 treatments. Primary outcome is
pain-ratings and function (The Knee Injury and Osteoarthritis Outcome Score (KOOS)).
Secondary outcome concerns various health-ratings and objective functional tests. Regarding
predictors for outcome, we plan also to investigate different psychosocial variables as well
as patient's beliefs regarding exercise. Feasibility of how high-dose exercise therapy
actually works in primary care health care settings is also planned to be reported.
Patients are being assessed by blinded assessor at inclusion, at end of intervention (3 mo),
and at six and 12 mo after end of treatment. We plan to include a total of 200 subjects from
primary health care settings, two in Norway and two in Sweden, with radiographic-verified
knee OA with knee pain and decreased function. The patients have to be within the 45 to 85
age group. Patients are excluded if they have been scheduled for knee surgery or have some
other form of illness/disease that limits the exercise tolerance (e.g. heart disease or
systemic/metabolic diseases or chronic obstructive airways disease). A major goal is to grade
exercises so that they are performed pain-free or close to pain-free in both intervention
groups. The principle of deloading is used to meet this goal using a high number of
repetitions in sets as pain modulation. The results from this study will give new information
about the effectiveness of graded exercise therapy in patients with knee OA, and new
knowledge if outcome can be related to the exercise dosage performed.
Osteoarthritis is one of the most common form of chronic diseases in the adult population,
and approximately 800 000 people in Sweden (population of approximately 9 million people)
suffer from this disease, which causes joint pain, stiffness, swelling, loss of function and
sick leave. Studies from Sweden, United Kingdom (UK) and USA show that costs for
osteoarthritis are about 1-2.5 % of GDP. With increasing life expectancies and the general
decrease in physical activity in western industrialized countries, it is expected that more
people will suffer from this disease. In a recent international literature review of clinical
studies on the effectiveness of exercise therapy, the authors concluded that there is some
evidence that therapeutic exercise is effective reducing knee pain and improving activities
of daily living. In a compilation of scientific studies by the Swedish Council on Technology
Assessment in Health Care (SBU), it was concluded that strength and flexibility exercises
resulted in positive short-term effects compared to information only. However, there is
currently no scientific study that has evaluated dose-response effects of exercise therapy.
To improve life quality for individuals with osteoarthritis and the use of exercise therapy
in primary and secondary health care settings, research on dose response effects in patients
with osteoarthritis is important. This view is supported by various systematic reviews
including the report from Swedish Council on Health Technology Assessment (SBU) latest
compilation.
Exercise dosage is a factor of exercise frequency, intensity and duration. Recent clinical
trials show positive effects at both short term-(end of intervention) and at long term follow
ups (6- and 12 months), in favor of high repetitive high dosage exercise therapy compared to
a relatively lower exercise dosage in patients with long-term subacromial pain and in
patients with long term patello femoral pain syndrome. Compared to treatment as usual,
exercise therapy has also been shown to be effective as postsurgical rehabilitation after
arthroscopic surgery in patients with knee pain with a verified ruptured mensicus. In this
present clinical trial, which is a Nordic collaborative project with researchers from
different research groups in Sweden and Norway, we intend to investigate short and long-term
effects comparing high dosage exercise therapy versus a low repetitive low dosage exercise
program in patients diagnosed with knee osteoarthritis. Primary outcome is pain (VAS) and
knee function (The Knee Injury and Osteoarthritis Outcome Score (KOOS)). Since it is unknown
which patients will respond to the different exercise dosages, we will also look at different
prognostic factors related to patient`s beliefs regarding exercise therapy as well as
different psychosocial variables as anxiety, depression, fear of movement, catastrophizing,
life satisfaction and level of self-efficacy. We hope this study will increase our knowledge
regarding positive and negative predictors for outcome.
Thus, the main aim of the study is to evaluate two modes of exercise therapy focusing on
exercise dosage; 1) exercise therapy with an exercise dosage lasting 80 - 90 minutes duration
at each treatment compared to; 2) low dosage exercise therapy (conventional exercise
treatment) lasting 20-30 minutes at each treatment) in patients with long-term knee
osteoarthritis. All patients in both intervention groups will receive three treatments a week
for 12 weeks making a total of 36 treatments. Physiotherapists at four different intervention
centers will treat patients from both exercise interventions. Assessments will be performed
at inclusion, after end of treatment, and at six and 12 months follow up. Objective tests (20
meter walk test, sit to stand in 30 seconds and maximum number of single knee
flexion/extension in 30 seconds) is tested out at inclusion and at end of treatment. The
testers are blinded regarding intervention group. Questionnaires are filled out by the
patient at inclusion, end of treatment, at six and 12 months follow up. To assess when
possible clinical interesting changes start to occur during the three month treatment period,
patients are filling out KOOS (function) and VAS (pain) after every 6th treatment making a
total of six measurements during the intervention period.
Patients are recruited from primary care health care settings in Västervik and Luleå in
Sweden and in Trondheim and Mosjöen in Norway. Patients are informed about the project both
verbally and also through written information. Based on this information, patients that would
like to participate in the project, contact the local investigation center to be assessed for
possible inclusion. We are planning to include a total of 200 patients with
radiographic-verified knee osteoarthritis with knee pain and decreased function. The patients
have to be within the 45 to 85 age group, come for three treatments a week, a total of 36
treatments for 12 weeks, and must not have had any treatments or organized form of exercise
therapy for their knee pain the last three months. Patients are also excluded if they have
been scheduled for knee surgery or have some other form of illnesses/disease that limits
exercise tolerance (e.g. heart disease or systemic/metabolic diseases or chronic obstructive
airways disease). Patients that fulfill the inclusion criteria will be randomized either to
high dosage medical exercise therapy or low dosage exercise therapy.
Each treatment in the high dosage group (also called "Medical Exercise Therapy, MET) consist
of 20 minutes global exercise (e.g. stationary cycling), then four local knee exercises
either open or closed chain performing three sets of 30 repetitions or five minutes
continuous repetitions, then another five minutes cycling followed by another four local knee
exercises three sets of 30 repetitions or five minutes continuous repetitions and finishing
with 10 minutes cycling. Each treatment lasts 80 to 90 minutes. The patients in this group
shall also perform one home exercise every day performing three sets of five minutes deloaded
knee extension with therabands. In the low dosage exercise group the patients perform a total
of five exercises; 10 minutes warm up using a stationary bicycle, then four different knee
exercises performing two sets of 10 repetitions. Each treatment last 20 to 30 minutes.
For all patients in both intervention groups the same methods are applied for testing out
exercises at the start of the treatment, and for grading exercises during the treatment
period. A major goal is to grade exercises so that they are performed pain-free or close to
pain-free in both intervention groups. The exercises are standardized for both exercise
programs, however individualized and graded continuously in relation to the patient's
clinical status. All treatments are carried out under the supervision of experienced and
skilled physiotherapists.
The treating physiotherapists are instructed to be neutral regarding their beliefs of which
treatment they believe is most effective informing the patient; in this study we are
comparing two different forms of exercise therapy and we do not know if one exercise mode is
better than the other or if they have equal effects.
The theoretical basis for MET and the exercise progressions have been described in scientific
articles and book chapters. Self-assessed pain, function and quality of life are monitored
both during treatment and after treatment, and at six and 12 months follow-up. Prognostic
markers evaluated by following analyze background information and early test results relate
to the long-term treatment outcome. Analysis of cost-effectiveness will be done using the
incremental cost-effectiveness ratio (ICER), in order to provide a single measure for
weighing costs against effects of the exercise dosage interventions. An assessment will also
be made for the cost per quality-adjusted life year (QALYs).
Our project team has extensive experience with the practical implementation of clinical
controlled studies and analytical methodology linked to registries and health economic cost
estimates. From this study we expect increased knowledge of whether clinical outcomes from
exercise therapy may be related to exercise dosage and how exercise therapy need to be
individualized according to the patient's history, clinical picture and coping strategies
obtaining. In a recent report from the Swedish Council on Health Technology Assessment (SBU)
they requested such data evaluating both the effects of exercise treatment analyzes that
support personalized rehabilitation.
The results from this study will give new information about the effectiveness of exercise
therapy for patients with knee osteoarthritis, and new knowledge if outcome can be related to
the dosage of exercise performed.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04651673 -
Prescribed Knee Brace Treatments for Osteoarthritis of the Knee (Knee OA)
|
||
Completed |
NCT05677399 -
Knee Osteoarthritis Treatment With Peloidotherapy and Aquatic Exercise.
|
N/A | |
Active, not recruiting |
NCT04043819 -
Evaluation of Safety and Exploratory Efficacy of an Autologous Adipose-derived Cell Therapy Product for Treatment of Single Knee Osteoarthritis
|
Phase 1 | |
Recruiting |
NCT06000410 -
A Study to Evaluate the Efficacy of Amniotic Suspension Allograft in Patients With Osteoarthritis of the Knee
|
Phase 3 | |
Completed |
NCT05014542 -
Needling Techniques for Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT05892133 -
Prehabilitation Effect on Function and Patient Satisfaction Following Total Knee Arthroplasty
|
N/A | |
Recruiting |
NCT05528965 -
Parallel Versus Perpendicular Technique for Genicular Radiofrequency
|
N/A | |
Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
Active, not recruiting |
NCT02003976 -
A Randomized Trial Comparing High Tibial Osteotomy Plus Non-Surgical Treatment and Non-Surgical Treatment Alone
|
N/A | |
Active, not recruiting |
NCT04017533 -
Stability of Uncemented Medially Stabilized TKA
|
N/A | |
Completed |
NCT04779164 -
The Relation Between Abdominal Obesity, Type 2 Diabetes Mellitus and Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT04006314 -
Platelet Rich Plasma and Neural Prolotherapy Injections in Treating Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT05423587 -
Genicular Artery Embolisation for Knee Osteoarthritis II
|
N/A | |
Enrolling by invitation |
NCT04145401 -
Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCK
|
||
Active, not recruiting |
NCT03781843 -
Effects of Genicular Nerve Block in Knee Osteoarthritis
|
N/A | |
Completed |
NCT05974501 -
Pre vs Post Block in Total Knee Arthroplasty (TKA)
|
Phase 4 | |
Completed |
NCT05324163 -
Evaluate Efficacy and Safety of X0002 in Treatment of Knee Osteoarthritis
|
Phase 3 | |
Completed |
NCT05529914 -
Effects of Myofascial Release and Neuromuscular Training for Pes Anserine Syndrome Associated With Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT05693493 -
Can Proprioceptive Knee Brace Improve Functional Outcome Following TKA?
|
N/A | |
Not yet recruiting |
NCT05510648 -
Evaluation of the Effect of High-intensity Laser Therapy in Knee Osteoarthritis
|
N/A |