Status:

COMPLETED

Mechanisms Underlying Local and Systemic Effects of Massage

Lead Sponsor:

Esther Dupont-Versteegden

Collaborating Sponsors:

University of Oklahoma

National Center for Complementary and Integrative Health (NCCIH)

Conditions:

Muscle Atrophy

Eligibility:

All Genders

18-30 years

Phase:

NA

Brief Summary

The purpose of this study is to determine whether massage can attenuate the loss of muscle mass in humans after a short period of disuse.

Detailed Description

The loss of skeletal muscle mass is a common symptom associated with diseases such as cancer, AIDS, diabetes, and congestive heart failure, and with aging. Muscle atrophy is associated with poor disea...

Eligibility Criteria

Inclusion

  • Men and women 18-30 years of age.
  • All races and ethnic backgrounds.
  • Non-smoker and generally healthy.

Exclusion

  • 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.

Key Trial Info

Start Date :

August 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2023

Estimated Enrollment :

44 Patients enrolled

Trial Details

Trial ID

NCT04131712

Start Date

August 1 2020

End Date

June 1 2023

Last Update

May 21 2024

Active Locations (1)

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University of Kentucky

Lexington, Kentucky, United States, 40536