- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01688622
Glypican4 and CTRP5 in Metabolic Syndrome and the Effect of Exercise on These Adipokines
September 20, 2012 updated by: K. M. Choi, Korea University
Effects of Exercise on Glypican4,CTRP3,5 and RBP4 Levels and Circulating Levels of These Adipokines in the Subjects With or Without Metabolic Syndrome
Glypican4, CTRP3, CTRP5 are emerging novel adipokines mediating obesity and inflammation related disorders.
RBP4 and adiponectin are well known important adipokines.
Therefore, we examine the circulating levels of theses adipokines in the subjects with or without metabolic syndrome.
Furthermore, we tried to clarify the effect of exercise on the circulating these adipokines.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
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 Locations
-
-
-
Seoul, Korea, Republic of
- Korea University Guro Hospital
-
-
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
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Women between 30 and 60 years of age who had a body mass index (BMI) more than 25 kg/m2
- The subjects of metabolic syndrome and age, gender matched non metabolic syndrome among the participants of Korean SO Study (KSOS) study, which is an ongoing epidemiologic study supported by the Korea Science and Engineering Foundation
Exclusion Criteria:
- participants had a history of cardiovascular disease
- any type of diabetes
- stage 2 hypertension
- malignant disease, severe renal, or hepatic disease
- Subjects taking medications that might affect body weight or body composition
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
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Exercise
obese women who are volunteers for the 3 months exercise programs
|
training session consisting of a brief warm-up, followed by an approximately 45-min session of aerobic exercise at an intensity of 60-75% of the age-predicted maximum heart rate (approximately 300 kcal/day) and a 20-min muscle strength train- ing programme (approximately 100 kcal/day), followed by a brief cool-down period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The changes of circulating glypican4 levels after 3 months exercise
Time Frame: baseline and 12weeks
|
baseline and 12weeks
|
|
The changes of circulating CTRP3 levels after 3 months exercise
Time Frame: baseline and 12weeks
|
baseline and 12weeks
|
|
The changes of circulating CTRP5 levels after 3 months exercise
Time Frame: baseline and 12weeks
|
baseline and 12weeks
|
|
The changes of circulating RBP4 levels after 3 months exercise
Time Frame: baseline and 12weeks
|
baseline and 12weeks
|
|
The changes of circulating adiponectin levels after 3 months exercise
Time Frame: baseline and 12weeks
|
baseline and 12weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Circulating glypican4 levels in the subjects with or without metabolic syndrome
Time Frame: baseline
|
baseline
|
|
Circulating CTRP3 levels in the subjects with or without metabolic syndrome
Time Frame: baseline
|
baseline
|
|
Circulating CTRP5 levels in the subjects with or without metabolic syndrome
Time Frame: baseline
|
baseline
|
|
Circulating RBP4 levels in the subjects with or without metabolic syndrome
Time Frame: baseline
|
baseline
|
|
Circulating adiponectin levels in the subjects with or without metabolic syndrome
Time Frame: baseline
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Choi HY, Park JW, Lee N, Hwang SY, Cho GJ, Hong HC, Yoo HJ, Hwang TG, Kim SM, Baik SH, Park KS, Youn BS, Choi KM. Effects of a combined aerobic and resistance exercise program on C1q/TNF-related protein-3 (CTRP-3) and CTRP-5 levels. Diabetes Care. 2013 Oct;36(10):3321-7. doi: 10.2337/dc13-0178. Epub 2013 Jun 18.
- Yoo HJ, Hwang SY, Cho GJ, Hong HC, Choi HY, Hwang TG, Kim SM, Bluher M, Youn BS, Baik SH, Choi KM. Association of glypican-4 with body fat distribution, insulin resistance, and nonalcoholic fatty liver disease. J Clin Endocrinol Metab. 2013 Jul;98(7):2897-901. doi: 10.1210/jc.2012-4297. Epub 2013 Apr 30.
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
July 1, 2012
Primary Completion (Actual)
September 1, 2012
Study Completion (Actual)
September 1, 2012
Study Registration Dates
First Submitted
September 13, 2012
First Submitted That Met QC Criteria
September 19, 2012
First Posted (Estimate)
September 20, 2012
Study Record Updates
Last Update Posted (Estimate)
September 21, 2012
Last Update Submitted That Met QC Criteria
September 20, 2012
Last Verified
September 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KoreaSO_Exercise
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.