Effects of Diet Control and Resistance Exercise Training on Obesity Adults With Knee Osteoarthritis

August 4, 2021 updated by: yenyen0411, Chang Gung Memorial Hospital

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

The purpose of this study was to investigate the effects of obesity on knee degenerative arthritis on body composition after dietary control and elastic resistance exercise; and whether persistent exercise habits and dietary control can relieve pain and strengthen muscle strength. Improve the quality of life and the decline of other risk factors.

Study Overview

Detailed Description

Due to dietary westernization and overweight, the number of knee joint degeneration is increasing year by year. Degeneration of knee arthritis can lead to pain and not exercise, and thus other chronic diseases. When the weight loss exceeds 5.1%, the function of the knee joint can be significantly improved and low heat weight loss (1200 kcal / day) and very low heat weight loss (less than 800 kcal / day) both weight loss The results are equally good .Many studies have shown that early and mid-interventional resistance exercise can improve muscle weakness, pain and stiffness in patients with degenerative knee arthritis, and elastic resistance exercise can effectively improve lower limb function and increase physical activity in patients with knee arthritis However, there has been no research on the effects of diet control and resistance exercise training on pain relief, body composition, lower limb function and quality of life in obese knee degenerative arthritis. The purpose of this study was to explore the degenerative knee degeneration. The effect of arthritis on the composition of the body after a balanced diet calorie control and home-based low-intensity elastic resistance movement; and whether persistent exercise habits and diet control can relieve pain, strengthen muscle strength, improve quality of life and other risks The effect of factor decline. Expected to combine the diet control and home group exercise to improve the quality of life of patients with degenerative knee arthritis.

Study Type

Interventional

Enrollment (Anticipated)

90

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Republic OF China
      • Taipei, Taiwan, Republic OF China, Taiwan, 10507
        • Recruiting
        • Chang Gung Medical Foundation
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

55 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • Low oil balanced diet 1200 kcal / day
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:
  • Low oil balanced diet 1200 kcal / day
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:
  • Low oil balanced diet 1200 kcal / day

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

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: YEN-I HSU, Chang Gung Medical Foundation

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 3, 2018

Primary Completion (Anticipated)

December 31, 2023

Study Completion (Anticipated)

December 31, 2023

Study Registration Dates

First Submitted

May 30, 2019

First Submitted That Met QC Criteria

June 2, 2019

First Posted (Actual)

June 4, 2019

Study Record Updates

Last Update Posted (Actual)

August 5, 2021

Last Update Submitted That Met QC Criteria

August 4, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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