Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT06053229

Effect of Percussive Massage on Skeletal Muscle During Limb Immobilization

Led by Brigham Young University · Updated on 2024-08-13

36

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary aims of this study are to determine the effect of percussive massage (30 min/session, 2 sessions/day, daily) during 10 days of unilateral limb immobilization on preserving muscle, vascular, and mitochondrial function. The following hypotheses will be tested: Hypothesis 1: Percussive massage will attenuate the loss of size, strength and endurance over the immobilization period compared to the control group, as measured by MRI, maximal isometric and isokinetic force production and muscle endurance test using Biodex dynamometry. Hypothesis 2: Percussive massage will attenuate the loss of vascular function and blood flow compared to the control group as measured by passive leg movement and femoral artery blood flow. Hypothesis 3: Percussive massage will attenuate the loss of skeletal muscle mitochondrial function and decrease H2O2 production during immobilization compared to the control group, as measured by high-resolution respirometry.

CONDITIONS

Official Title

Effect of Percussive Massage on Skeletal Muscle During Limb Immobilization

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 50 years, women must be pre-menopausal
  • Stable physical activity levels for at least 6 months
  • No previous lower leg injury preventing knee extension exercises
Not Eligible

You will not qualify if you...

  • Current cigarette or marijuana smoker
  • Pregnant or planning pregnancy within one month
  • Diagnosed cardiovascular, metabolic, or cognitive diseases
  • Taking prescribed medications or anti-depressants
  • Regular use of massage or vibration on the thigh
  • Unable to understand and provide informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Brigham Young University

Provo, Utah, United States, 84602

Actively Recruiting

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Research Team

R

Robert D Hyldahl, PhD

CONTACT

T

Ty Hopkins, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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