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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04750694
Other study ID # VEK ID 74646
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2020
Est. completion date November 1, 2021

Study information

Verified date February 2021
Source Department of Public Health, Denmark
Contact Simon Lønbro, PhD
Phone 004521600410
Email loenbro@ph.au.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose of the study is: to investigate the effects of 8 weeks intervention of high intensity resistance training(HIRT) combined with Blood Flow Restricted Exercise (BFRE) compared to high intensity resistance training alone. Detailed Description: 30 elite handball players will be randomized into 2 groups of 15 participants each. Participants will be evaluated in the week before and the week after an 8-weeks training intervention with 2 weekly sessions. Based on their baseline muscle strength the participants will be randomized into two groups: HIRT-BFRE or HIRT-HIRT. Participants in both groups will perform a full-body training programme of HIRT. After the Full-body programme, Back squat exercise with low intensity and Blood flow restriction will be performed to the HIRT-BFRE group and back squat exercise with high intensity without blood flow restriction will be performed by HIRT-HIRT. Evaluation protocol includes: muscle strength measurement with 1 repetition maximum of Back squat and knee extension, muscle mass with Dual-Energy X-ray absorptiometry, muscle thickness of the thigh with ultra sound measurement, vertical jump height with linear Encoder, sprint performance with 30m sprint time.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date November 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Age >= 18 years - Ds - Minimum of 2 years of resistance training experience - >< Two resistance training sessions each week - >< three handball sessions each week - No injuries that prevent participants to perform test of maximal muscle strength - No injuries, that affects the muscle strength or the ability to train Exclusion Criteria: - Elevated blood pressure (>140/90) - Anabolic steroids or prescription-only medical products with know or potential effect on muscle hypertrophy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Resistance training
A full-training programme with high intensity followed by back squat exercise with blood flow restriction. Inflatable cuffs will be placed proximally on both thighs. The cuff pressure will be 50% of individual arterial occlusion pressure and will be maintained during the rest intervals. Participants will perform 30, 15, 15 and 15 repetitions of 30% of 1 Repetition Maximum. Totally 75 repetitions will be performed. 45 seconds rest interval between sets will be given.

Locations

Country Name City State
Denmark Dept. of Public Health Aarhus

Sponsors (1)

Lead Sponsor Collaborator
Department of Public Health, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Jump Performance Change in jump height. Change in vertical jump height (in cm, with Chronojump Linear Encoder Kit). Participants will perform a counter movement jump and jump as high as possible. The jump height will be recorded. Baseline measurements at week 1 and post intervention at week 10.
Other Sprint performance Sprint performance. Change in sprint time (in seconds, with Witt speed gates). Participant will perform a 30-meter sprint on an indoor handball court. The time to perform a 30-meter sprint will be recorded. Baseline measurements at week 1 and post intervention at week 10.
Primary Change in Maximal Muscle Strength Change in 1 RM (repetition maximum) muscle strength in back squat Baseline measurements at week 1, after four weeks of exercise at week 5 and post intervention at week 10.
Secondary Change in Lean body mass Change in lean body mass assessed by Dual Energy X-ray Absorptiometry Baseline measurements at week 1 and post intervention at week 10.
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