Mechanisms Underlying Local and Systemic Effects of Massage
Muscle Atrophy
About this trial
This is an interventional supportive care trial for Muscle Atrophy focused on measuring Massage, Muscle, Extracellular Vesicles, Atrophy
Eligibility Criteria
Inclusion Criteria:
- Men and women 18-30 years of age.
- All races and ethnic backgrounds.
- Non-smoker and generally healthy.
Exclusion Criteria:
- Have a current lower extremity musculoskeletal injury or compromised musculoskeletal function that would not allow the safe use of crutches or a brace.
- Previous lower extremity surgeries or injury.
- Activities of daily living require long periods of standing or driving a manual transmission car.
- Body mass index (BMI) under 27.
- Evidence or signs and symptoms of metabolic syndrome or disorder (diagnosis of diabetes or insulin resistance, elevated BP, high fasting blood sugar, abnormal cholesterol or triglyceride levels).
- Thyroid disorder.
- Acute or chronic infections.
- Use of systemic steroids, anabolic steroids, or growth hormone.
- Chronic aspirin or NSAID use (unless it can be safely stopped prior to the biopsies), and any other use of an anticoagulant (e.g., Coumadin) or history of bleeding including history of hypo- or hyper-coagulation disorders.
- Lidocaine allergy (1% lidocaine is the local anesthetic used during the muscle biopsy procedure).
- Any other condition or events considered exclusionary by the PI and/or physician, such as non-compliance.
- Pregnancy.
Sites / Locations
- University of Kentucky
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
Sham Comparator
No Intervention
Experimental
Ambulatory Control
Ambulatory Massage
Immobilization Control
Immobilization Massage
Following baseline assessments, participants will be randomized into the ambulatory group for the remainder of the study. Atrophy will not be induced and massage intervention will not be applied. Ambulatory groups will be recruited following the immobilized groups.
Following baseline assessments, participants will be randomized into the ambulatory group for the remainder of the study. No atrophy induction. Four massage treatments will be applied every other day until the end of the study. Ambulatory groups will be recruited following the immobilized groups.
Following baseline assessments, participants will be randomized into the unilateral lower limb suspension group undergoing atrophy for the remainder of the study. Massage intervention will not be applied.
Following baseline assessments, participants will be randomized into the unilateral lower limb suspension group undergoing atrophy for the remainder of the study. Four massage treatments will be applied every other day until the end of the study.