- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03973463
Effects of Diet Control and Resistance Exercise Training on Obesity Adults With Knee Osteoarthritis
Effects of Diet Control and Resistance Exercise Training on Obesity Adults With Knee Osteoarthritis in Pain Relief, Body Composition, Lower Limb Function and Quality of Life
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: YEN-I HSU
- Phone Number: 8436 07-7317123
- Email: yenyen0411@cgmh.org.tw
Study Locations
-
-
Republic OF China
-
Taipei, Taiwan, Republic OF China, Taiwan, 10507
- Recruiting
- Chang Gung Medical Foundation
-
Contact:
- shui tseng
- Phone Number: 3706 03-3196200
- Email: tsengshui@cgmh.org.tw
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Cases of knee joint degeneration diagnosed by orthopedics, rheumatology and immunology physicians.
- X-ray interpretation (kellgren & Lawrence grade) grades 1 to 3 or mild to moderate patients.
- Willing to sign written consent form.
- Pain Index (VAS) ≧ 4/10.
- Men and women over the age of 55.
- Body mass index (BMI) ≧ 27 kg/m^2.
Exclusion Criteria:
- Unable to act on your own.
- X-ray interpretation (kellgren & Lawrence level) is greater than level 3 or is a serious level.
- Patients who have undergone knee arthroplasty on one or both feet.
- Patients with terminal liver and kidney disease.
- Those who are unable to perform physical function measurement after severe diagnosis of heart and lung disease after diagnosis by the physician.
- High blood pressure with poor control (systolic blood pressure greater than or equal to 180 mmHg at the time of return).
- Pregnant women or breastfeeding women.
- Those who have coronary stents, cardiac rhythms, or other metallic substances in the body are not recommended for total body composition analysis.
- Those with severe hip, knee, and lower back pain who are unable to perform exercise, other neuromuscular, skeletal joints, or rheumatic diseases may be exacerbated by exercise. Or those who have musculoskeletal injuries in the past six months (such as bruises, fractures, etc.).
- Unable to cooperate with the test or halfway through the test.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: Low fat diet,12 weeks low oil balance 1200 kcal / day
12 weeks low oil balance 1200 kcal / day
|
Low resistance (7kg and 10kg) elastic band exercise 3 times a week for 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.
Other Names:
|
|
Experimental: 12-week resistance exercise 3 times a week
12-week stretch with resistance exercise, 3 times a week
|
Low resistance (7kg and 10kg) elastic band exercise 3 times a week for 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.
Other Names:
|
|
Experimental: 12 weeks low oil balance and resistance exercise
12 weeks low oil balance 1200 kcal / day and 12-week stretch with resistance exercise, 3 times a week
|
Low resistance (7kg and 10kg) elastic band exercise 3 times a week for 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.Balanced diet reduces oil intake by 1200 calories per day.
Maintains 12 weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
WOMAC
Time Frame: Baseline and after 3 months
|
WOMAC is used to measure the patient's home knee function. Each question is scored using a five-point scale. The higher the score, the worse the knee function. This study assessed the amount of change in WOMAC scores, whether it was lower than baseline after 12 weeks. |
Baseline and after 3 months
|
|
KOOS
Time Frame: Baseline and after 3 months
|
KOOS is based on WOMAC and covers a wider range.
The score of each topic is 0-4 points.
The higher the score after the conversion formula, the better the knee joint function.
This study assessed changes in KOOS scores, whether it was higher than baseline after 12 weeks.
|
Baseline and after 3 months
|
|
Body fat percentage
Time Frame: Baseline and after 3 months
|
Assess the amount of body fat (%) change, whether it can be less than baseline after 12 weeks
|
Baseline and after 3 months
|
|
Body Mass Index
Time Frame: Baseline and after 3 months
|
Assess the amount of Body Mass Index(kg/m^2) change, whether it can be less than baseline after 12 weeks
|
Baseline and after 3 months
|
|
waistline
Time Frame: Baseline and after 3 months
|
Waist circumference change from baseline to 12 weeks (cm)
|
Baseline and after 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hand grip force measurement
Time Frame: Baseline and 3 months
|
Easy to stand.
Used to grasp the grip
|
Baseline and 3 months
|
|
2.44m time up to go
Time Frame: Baseline and 3 months
|
Stand up when you hear the start password.
Use the brisk walk to bypass the marker point and then return to the chair to sit down.
|
Baseline and 3 months
|
|
30 chair stand test
Time Frame: Baseline and 3 months
|
Sit down and stand up to stand upright, then quickly return to sit down for an action, within 30 seconds
|
Baseline and 3 months
|
|
total cholesterol
Time Frame: Baseline and 3 months
|
Cases will be tested for total cholesterol (mg/dL) in routine outpatient care. This study, at baseline and 12 weeks later, copied the most recent total cholesterol report from the case. The amount of change in total cholesterol after baseline and 12 weeks was compared. |
Baseline and 3 months
|
|
Low-density cholesterol
Time Frame: Baseline and 3 months
|
Cases in the outpatient routine care will be blood tests for low-density cholesterol (LDL-C, mg / dL), the study of the most recent low-density cholesterol report from the case at baseline and 12 weeks later, compared with baseline and 12 weeks later Low-density cholesterol has changed.
|
Baseline and 3 months
|
|
triglyceride
Time Frame: Baseline and 3 months
|
Cases will be tested for triglycerides (mg/dL) in routine outpatient care. In the study, at the baseline and after 12 weeks, the most recent triglyceride report from the case was copied. The amount of change in triglyceride at baseline and after 12 weeks was compared. |
Baseline and 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: YEN-I HSU, Chang Gung Medical Foundation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201800607B0
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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