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IRCT20181006041252N11 IRCT 2019-05-21 Sabzevar University of Medical Sciences Effects of combined aerobic-resistance exercise training on levels of Chemerin and Omentin in men with type 2 diabetes Investigating the effects of combined aerobic-resistance exercise training on levels of Chemerin and Omentin in men with type 2 diabetes 2015-04-13 anticipated 24 Complete https://irct.ir/trial/39698 interventional Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Randomization was conducted based on a permutation block by a statistical consultant using random allocation software and the output sequences A and B are available to the researcher, Accordingly, 6 blocks were allocated to patients, in each block, 2 from A treatment group, 2 from the B treatment group were placed. Eventually, after completing the blocks group A was trained with combined aerobic-resistance exercise, Group B does not receive any special treatment (control). First, we determine all sixsome modes in which two individuals are assigned to group A and two to group B. Then we assign one of the digits 1 to 6 to each of the sixsome combinations (which includes thirty-six modes). In the next step, we must randomly select 6 blocks of six and write their combinations in succession. For this we have to make 6 samplings with replacement from a six-member community; 6 times, choose a random number between 1 and 6 and this process will continue until the end of the sampling and the difference between the two groups will not exceed a maximum of two (half the size of the block). 3 Type 2 diabetes. Intervention 1: Intervention group: The training group will undergo combined aerobic-resistance exercise training with distinct intensity for 12 weeks, three sessions a week. Each training session will include 5 to 10 minutes of warm-up, 45 minutes of resistance training, 30 minutes of aerobic training, respectively. In order to measure the biochemical variables, the blood sampling is performed after 12 hours of fasting and in two steps before the start of the training program and after 12 weeks. Subjects are asked to do no severe activity for two days prior to blood sampling. Intervention 2: Control group: control subjects also only perform their routine activities. In order to measure the biochemical variables, the blood sampling is performed after 12 hours of fasting and in two steps before the start of the training program and after 12 weeks. Subjects are asked to do no severe activity for two days prior to blood sampling. No - There is not a plan to make this available Justification or reason for not sharing IPD is No more information
public Dr. Mehdi Zarei
Sabzevar University of Medical Sciences, Tohid Blvd., Sabzevar Town
Sabzevar Iran (Islamic Republic of) 9617913114 +98 51 4401 1604 Zarei.m8716@yahoo.com Sabzevar University of Medical Sciences scientific Dr. Mehdi Zarei
Sabzevar University of Medical Sciences, Tohid Blvd., Sabzevar Town
Sabzevar Iran (Islamic Republic of) 9617913114 +98 51 4401 1604 Zarei.m8716@yahoo.com Sabzevar University of Medical Sciences Iran (Islamic Republic of) Lack of cardiovascular, musculoskeletal, and metabolic disorders limiting exercise Lack of high blood pressure Lack of regular exercise activity in the last 6 months Not receiving insulin 30 years 60 years Male Inability to perform exercises Having regular sports activities rather than research exercises E08 Diabetes mellitus due to underlying condition Treatment - Other Treatment - Other Intervention group: The training group will undergo combined aerobic-resistance exercise training with distinct intensity for 12 weeks, three sessions a week. Each training session will include 5 to 10 minutes of warm-up, 45 minutes of resistance training, 30 minutes of aerobic training, respectively. In order to measure the biochemical variables, the blood sampling is performed after 12 hours of fasting and in two steps before the start of the training program and after 12 weeks. Subjects are asked to do no severe activity for two days prior to blood sampling. Control group: control subjects also only perform their routine activities. In order to measure the biochemical variables, the blood sampling is performed after 12 hours of fasting and in two steps before the start of the training program and after 12 weeks. Subjects are asked to do no severe activity for two days prior to blood sampling. Determine the levels of chemerin. Timepoint: At the beginning of the study (before the intervention) and 12 weeks after the start of the training program. Method of measurement: Use of Luminescence quantitative and ELISA methods. Determine the level of omentin. Timepoint: At the beginning of the study (before the intervention) and 12 weeks after the start of the training program. Method of measurement: Use of Luminescence quantitative and ELISA methods. Sabzevar University of Medical Sciences Approved 2015-04-13 Ethics committee of Sabzevar University of Medical Sciences Sabzevar University of Medical Sciences, Tohid Blvd, Sabzevar city Sabzevar Razavi Khorasan Iran (Islamic Republic of)