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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05958056
Other study ID # 4/2019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2021
Est. completion date July 1, 2022

Study information

Verified date August 2023
Source University of Jordan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Practical blood flow restriction (PBFR) is a new technique of reducing the venous return using a band with a pressure that is applied using a perceived pressure scale. The studies that investigate the acute effect of using PBFR and regular high intensity exercises on the level of growth hormone (GH) and blood lactate (BL) after lower extremity training in collegiate athletes are scarce.


Description:

Practical blood flow restriction (PBFR) is a new technique of reducing the venous return using a band with a pressure that is applied using a perceived pressure scale. The studies that investigate the acute effect of using PBFR and regular high intensity exercises on the level of growth hormone (GH) and blood lactate (BL) after lower extremity training in collegiate athletes are scarce. Therefore, this study aimed to investigate the acute effect of a single session low load resistance exercises with PBFR compared to a high load resistance exercises without PBFR on the levels of GH and BL. A convenience sample of collegiate athletes were allocated to either an experimental group that performed low resistance exercises with PBFR or a control group that performed high resistance exercises without PBFR. The levels of GH and BL were examined in 3 time points: pre-training, immediate post-training, and 15 minutes post-training for both groups. Analysis of Variance (ANOVA) was used to assess the main and interaction effects of the groups.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date July 1, 2022
Est. primary completion date December 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Student collegiate athletes. - Age of 18 years and older. - Free from any cardiovascular or respiratory disorders and did not have any injuries during the previous 12 months. Exclusion Criteria: - Students who were taking any medications for chronic conditions. - Student who were taking any supplements.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance exercise
The training session included leg curl and leg extension exercises with 4 sets each. Participants started with leg extension exercise for 4 sets with a 30-second rest periods between the sets. Then, participants took a rest for 60 seconds. Afterward, participants performed leg curl exercise for 4 sets with a 30-second rest periods between the sets. Exercises in each set were performed continuously (uninterrupted) with a speed of 2 seconds for each repetition and a medium exercise performance speed.

Locations

Country Name City State
Jordan The University of Jordan Amman

Sponsors (2)

Lead Sponsor Collaborator
University of Jordan The Hashemite University

Country where clinical trial is conducted

Jordan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Growth Hormone Blood test of the level of growth hormone Before intervention.
Primary Growth Hormone Blood test of the level of growth hormone Immediately post intervention.
Primary Growth Hormone Blood test of the level of growth hormone 15 minutes after the end of intervention.
Primary Blood lactate Blood test of the level of Blood lactate Before intervention.
Primary Blood lactate Blood test of the level of Blood lactate Immediately post intervention.
Primary Blood lactate Blood test of the level of Blood lactate 15 minutes after the end of intervention.
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