Viewing Study NCT05504629



Ignite Creation Date: 2024-05-06 @ 6:00 PM
Last Modification Date: 2024-10-26 @ 2:39 PM
Study NCT ID: NCT05504629
Status: COMPLETED
Last Update Posted: 2022-08-24
First Post: 2022-08-13

Brief Title: Interindividual Postexercise Hypotension Response in Morbid Obesity
Sponsor: Universidad Nacional Andres Bello
Organization: Universidad Nacional Andres Bello

Study Overview

Official Title: Characterizing The Interindividual Postexercise Hypotension Response For Two Order of Concurrent Training In Patients With Morbid Obesity
Status: COMPLETED
Status Verified Date: 2022-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: A quasi-experimental study developed in sedentary morbidly obese men and women age 436113 y body mass index BMI 40 kgm2 were assigned to a CT group of ET plus RT ETRT n19 BMI 478167 or RT plus ET order group RTET n17 BMI 43080 Subjects of both groups received eight exercise sessions over four weeks Systolic SBP diastolic DBP mean arterial pressure MAP heart rate at rest HR and pulse pressure PP measurements before and after 10 minutes postexercise Secondary outcomes were other anthropometric body composition metabolic and physical condition parameters Using the SBP reduction and quartile categorization Q in high Rs quartile 4 moderate MRs quartile 3 low LRs quartile 2 and nonresponders NRs quartile 1 were reported
Detailed Description: Independent of the order ie ETRT or RTET each CT session had two sections RT and ET which were applied two days per week during 8 sessions 4 weeks and where the blood pressure changes were measured only in four opportunities ie once a week in sessions 2 4 6 and 8 Thus the CT included in each session 3 stages a callisthenics exercises b main exercise ETRT or RTET and c cool down exercises

Before the starting the participants were involved in the maximum strength capacity estimated using a submaximal test based on the Brzyckis equation weight 10278-00278repetitions that does not change based on the sex age of the population or the exercise modality that is performed Mayhew et al 2004 After this procedure there were applied 4 familiarization sessions that consisted in session 1 knowledge of all measurements knowledge of exercise-machine manipulation and instructions during the exercise program session 2 exercising during cycling weights and metal bars session 3 applying a few of exercises of RT in 2 to 3 sets of exercises to know the configuration of each exercise ie ET and RT regimes itself and session 4 applying the 50 to 70 of their CT program corresponding to a normal session compound In the calisthenic stage each subject developed 10 minute warm-up with continuous walking joint mobility and flexibility exercises In the main part of the session and independent of the CT order group ETRT or RTET the ET section consisted of continuous cycling using a magnetic resistance static bicycle OxfordTM Fitness model BE-2701 Chile for 20 minutes The intensity of the ET exercise was regulated through the previously used modified Borg scale from 1 to 10 rating of perceived exertion Gillen et al 2013 and the participants worked at a level between 5 to 7 points ie moderate-intensity considering the original 6 to 20 points scale Borg 1998 being the subjects regularly controlled to not exceed this intensity restriction On the other hand the RT section included 8 to 12 muscle strength exercises of circuit training with the following different muscle groups 1 forearm 2 knee flexors and extensors 3 trunk 4 chest 5 shoulder elevators 6 horizontal shoulder flexors 7 extensors and finally 8 plantar flexors These exercises were performed in one set in a continuous concentriceccentric voluntary contraction as possible for 60 seconds followed by 60 to 90 seconds of passive recovery where each participant was changed to another exercise The RT section was of 25 minutes in duration time

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None