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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04977804
Other study ID # 12042b
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date March 30, 2024
Est. completion date December 1, 2025

Study information

Verified date November 2023
Source Utah State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will determine the effects of adding blood flow restriction to eccentric training to assess whether this increases the improvements of muscle strength and size.


Description:

Subjects will be randomly assigned to two groups: an eccentric only resistance training group or an eccentric training plus blood flow restriction group. Subjects will train at a moderately low intensity on a multiple-joint eccentric device. Those in the blood flow restriction will wear blood flow restriction cuffs on their upper thighs to reduce blood flow during the brief protocol. The training session will occur twice per week and will last ~5 minutes, including a one minute warm up, a one minute cool down and a three minute workout phase. The training program will last 7 weeks. Testing will be conducted at baseline (following a one session familiarization), 4 weeks and after the end of the 7 week training period. Assessments will focus on muscle strength, function, and morphology (size).


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 1, 2025
Est. primary completion date June 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - 18-30 years of age - currently engaged in some form of resistance training between 1-3 times per week - must have been training aerobically, but no more than 3 hours a week for the past six months Exclusion Criteria: - Must not have had any surgery of the lower limbs within the past 1 year period - Must not have any neuromuscular disorder (e.g., Muscular dystrophy etc.) - < 76 inches tall (in order to fit on the training machine) - Maximal strength of < 725 lbs for the eccentric training device - If any of the subjects are pregnant or plan to be pregnant in the duration of the protocol. For those randomized to the BFR group, if any of the subject's thighs are too large for the BFR cuffs (greater than 68 cm).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
The interventions are a form or exercise, specifically resistance exercise.
Eccentric plus blood-flow restriction
Eccentric plus blood-flow restriction

Locations

Country Name City State
United States Utah State Universtiy Logan Utah

Sponsors (1)

Lead Sponsor Collaborator
Utah State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Eccentron maximal muscle strength Eccentric muscle strength will be assessed via Eccentron (BTE Technologies, Inc., USA), an seated isokinetic dynamometer. 7 weeks
Primary Local muscle hypertrophy Muscle size changes of the quadriceps muscle measured an ultrasound device (GE NextGen LOGIQ, Tampa, Florida, USA). 7 weeks
Primary Muscle mass dual energy x-ray absorptiometry device (DEXA) the Hologic Horizon W Dual X-ray absorptiometry (Hologic Canada ULC, Mississauga, ON, Canada) will be used to assess appendicular (lower body) mean mass. 7 weeks
Primary Muscle function Vertical jump height will assess 3 maximal countermovement attempts on a jump mat (Just Jump Technologies, Huntsville, AL, USA) that measures jump height based on flight time. 7 weeks
Secondary Muscle soreness local muscle soreness will be assessed throughout the duration of the intervention period using a Wagner force algometer. 7 weeks
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