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The Study of Neuromuscular Exercise Therapy and Patients Self-management Program in Knee Osteoarthritis

The Study of Neuromuscular Exercise Therapy and Patients Self-management Program in Knee Osteoarthritis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03363490
Enrollment
400
Registered
2017-12-06
Start date
2018-04-01
Completion date
2019-12-31
Last updated
2018-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Therapy

Keywords

Self-Management, Neuromuscular Exercise Therapy, Knee osteoarthritis

Brief summary

Osteoarthritis is the most common chronic disabling disease,the importance of patient's self-management in chronic disease has been paid more and more attention internationally. Currently, the self-management of OA patients in China is lack of instructions from professional clinicians, and leads to inappropriate excise, irregular drug medication. OAKP (Osteoarthritis of the Knee Self-Management Program) is a program initiated from University of Southern Denmark, follows clinical guidelines of OA, formatted for easy use by patients and clinicians, including customized neuromuscular exercise therapy, educational sessions of what is OA and how to control body weight to protect the knee. The main purpose of this study is to verify the effectiveness of neuromuscular exercise therapy and OAKP, see whether it can help patients to relief the symptom and improve life quality.

Detailed description

The study plans to enroll patients above 50 years old who suffered from knee OA, but patients meets any of the exclusion criteria will not be enrolled. 400 patients of knee OA will be randomly divided into A, B, C, D four parallel groups with fully informed, each group will enroll 100 patients, A for control group, B for neuromuscular exercise, C for self-management program, D for neuromuscular exercise and self-management program, respectively. Each collaborate hospital would enroll patients as a multicenter clinical trial. Patient will receive a baseline and 3m, 6m, 12m follow-up evaluation of their knee physical function. Primary outcome measure is KOOS (Knee Injury and Osteoarthritis Outcome Score), secondary evaluation include VAS, EQ-5D, Arthritis self-efficacy score, 6-minutes Walk test, TUG test, 20 meters quick walk test,Stand up test in 30 seconds, Balance test, Kellgren& Lawrence(KL), Pain medication. Outcome will compare the mean difference between baseline survey and 12 months of follow-up in each group, using t-test or chi-square test,respectively.

Interventions

Self-management diary will record the frequency of pain, fatigue and injury of knee joint due to knee OA, if patients maintain proper activities, it will be also recorded by an smart phone APP. Patients diet and intake calorie will also be recorded in the diary,which help clinicians to adjust their diet, control their body weight.

The exercise therapy is basically combined with neuromuscular training and anti resistance training. The aim is to improve the stability of the joints, enhance sensory motor control of lower extremities, reconstruct neutral position line. The exercise mode, frequency, intensity and duration will be adjusted individually through monitoring patient's pain.

BEHAVIORALHealth education

All four groups of patient will receive two times of health education in the first week.

Sponsors

Beijing Jishuitan Hospital
CollaboratorOTHER
General Hospital of Beijing PLA Military Region
CollaboratorOTHER
Peking Union Medical College Hospital
CollaboratorOTHER
Chinese Academy of Medical Sciences, Fuwai Hospital
CollaboratorOTHER
Peking University People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Assessor will not know which group the patients are enrolled when evaluate the baseline and follow-up situation

Intervention model description

Patients of knee OA will be divided into A, B, C, D four parallel groups with fully informed, each group will enroll 100 patients, A for control group, B for neuromuscular exercise, C for self-management program, D for neuromuscular exercise and self-management program, respectively.

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- 1.Clinical diagnosis of knee osteoarthritis, Diagnostic criteria is based on the Chinese medical association's 2007 diagnosis and treatment guidelines for osteoarthritis: 1. Repeated knee joint pain within 1 month; 2. X-ray(weight-bearing or not)shows narrowed joint space,sclerosis and (or) cystic degeneration of subchondral bone, osteophytes of the joints; 3. The joint fluid (at least twice) is clear and viscous, WBC\<2000个/ml; 4. Age of patients ≥40 yrs; 5. Morning stiffness≤3 min; 6. Bone friction in the activity; Note:Combine clinical feature, laboratory and X-ray examination,when the patients meet(1)+(2) or (1)+(3)+(5)+(6) or (1)+(4)+(5)+(6),they can be diagnosis as knee osteoarthritis. 2.VAS≥4分; 3.No surgical treatment is planned within 6 months;

Exclusion criteria

1. Other types of arthritis, such us RA(rheumatoid arthritis) 2. Severe deformity of knee joint; 3. Over obesity patients(BMI\>35); 4. Other comorbidities that would severely affect somatic function, such as: cerebral infarction, lumbar disease that meets surgical indications, lower extremity angiopathy; 5. Decompensated cardiac dysfunction; 6. Severe cardiovascular and cerebrovascular diseases, or the patient is too weak for any kinds of exercise; 7. Lack of compliance;

Design outcomes

Primary

MeasureTime frameDescription
The Western Ontario and McMaster Universities Osteoarthritis Index,WOMACBaseline, 3 months, 6 months, 12monthsWOMAC grade is a reliable knee osteoarthritis patients' self-reported therapeutic effect evaluation system, including three dimensions: pain, stiffness, daily activities and quality of life, and each dimension includes several questions scale from 0(worst) to 4(best) , total score of each dimension range from zero (worst) to 100 (best). Score of each question add together will be the total score. Baseline, 3 months, 6 months, 12 months, through visit or telephone follow-up will be recorded. Compare the mean difference of WOMAC grade between baseline survey and 12 months of follow-up in each group.

Secondary

MeasureTime frameDescription
Visual Analog Score(VAS)Baseline, 3 months, 6 months, 12monthsVisual Analogue Scale of pain is a scale to extimate pain, and its score ranges from 0(worst) to 10(best). The higher the score is, the more severe pain the patient is feeling.
EuroQol Five Dimensions Questionnaire(EQ-5D)Baseline, 3 months, 6 months, 12monthsEQ-5D is a scale to extimate health condition and quality of life, and its score ranges from -0.6 to 1.0. The higher the score is, the healthier the patient is.
Kellgren& Lawrence(KL)BaselineThe higher the KL score is ,the more severe the patient is. Baseline,through visit or telephone follow-up.

Countries

China

Contacts

Primary ContactYifan Chen
chenyifan_cn@163.com15810031180
Backup ContactRujun Li, Attending
15810963512

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026