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Clinical Trials/NCT05097092
NCT05097092UnknownNot Applicable

Strength Training Augmenting Rehabilitation - 1

Texas Christian University2 sites in 1 country20 target enrollmentStarted: August 13, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
20
Locations
2
Primary Endpoint
Changes in lean mass

Study Overview

Brief Summary

This project aims to determine whether a novel strength training rehabilitation protocol can diminish the negative consequences of limb immobilization and expedite the restoration of muscle function during retraining in healthy individuals.

Detailed Description

The present study will examine the time course of muscle strength and size adaptations in two groups of volunteers during immobilization and retraining. Both groups will undergo temporary muscle disuse by wearing a shoulder sling and swathe on their non-dominant arm for ~≥10 hours/day for four weeks. One group (immobilization + unilateral training) will perform progressive unilateral strength training of the free limb throughout the immobilization period. The other group (immobilization control) will not undergo any training during the immobilization period. Following immobilization, both groups will undergo four weeks of bilateral strength training to retrain the immobilized arm.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • a body mass index between 18 - 35 kg/m2
  • 18-35 years of age
  • right-hand dominant
  • willingness to comply with the immobilization requirements
  • willingness to refrain from strength training outside of the study
  • willingness to comply with the strength training procedures of the study

Exclusion Criteria

  • a personal or family history of blood clots
  • a personal or family history of thyroid disorders
  • previous orthopedic surgeries to the upper limbs and/or joint pain of the upper limbs in the last 6 months
  • neuromuscular or metabolic disorders
  • osteoarthritis
  • use of hormone replacement therapy (ie., testosterone, estrogen, and/or growth hormone pharmaceuticals)
  • pregnancy and/or nursing

Arms & Interventions

Immobilization control

Experimental

The immobilization control group will undergo arm immobilization. Immobilization will be implemented with four weeks of muscle unloading with a sling and swathe on the nondominant arm. The sling will suspend the arm at the elbow joint with the elbow in a flexed position at 90°, the swathe will then wrap around the participant to fix the arm against the body.

Intervention: Orthopedic immobilization (Procedure)

Immobilization control

Experimental

The immobilization control group will undergo arm immobilization. Immobilization will be implemented with four weeks of muscle unloading with a sling and swathe on the nondominant arm. The sling will suspend the arm at the elbow joint with the elbow in a flexed position at 90°, the swathe will then wrap around the participant to fix the arm against the body.

Intervention: Bilateral resistance training (Other)

Immobilization with unilateral training

Experimental

The immobilization with unilateral training group will undergo arm immobilization for four with a sling and swathe on the nondominant arm. The sling will suspend the arm at the elbow joint with the elbow in a flexed position at 90°, the swathe will then wrap around the participant to fix the arm against the body. The free (non-immobilzed) arm of this group will undergo heavy strength training twice per week throughout the immobilization period. The training will consist of unilateral dumbbell shoulder press and biceps curl.

Intervention: Orthopedic immobilization (Procedure)

Immobilization with unilateral training

Experimental

The immobilization with unilateral training group will undergo arm immobilization for four with a sling and swathe on the nondominant arm. The sling will suspend the arm at the elbow joint with the elbow in a flexed position at 90°, the swathe will then wrap around the participant to fix the arm against the body. The free (non-immobilzed) arm of this group will undergo heavy strength training twice per week throughout the immobilization period. The training will consist of unilateral dumbbell shoulder press and biceps curl.

Intervention: Unilateral resistance training (Other)

Immobilization with unilateral training

Experimental

The immobilization with unilateral training group will undergo arm immobilization for four with a sling and swathe on the nondominant arm. The sling will suspend the arm at the elbow joint with the elbow in a flexed position at 90°, the swathe will then wrap around the participant to fix the arm against the body. The free (non-immobilzed) arm of this group will undergo heavy strength training twice per week throughout the immobilization period. The training will consist of unilateral dumbbell shoulder press and biceps curl.

Intervention: Bilateral resistance training (Other)

Outcomes

Primary Outcomes

Changes in lean mass

Time Frame: Changes from baseline at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 weeks

DEXA

Changes in isometric muscle strength

Time Frame: Changes from baseline at 5 and 10 weeks

MVC (Newton)

Changes in dynamic muscle strength

Time Frame: Changes from baseline at 5 and 10 weeks

1RM (lbs)

Changes in muscle size

Time Frame: Changes from baseline at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 weeks

Ultrasound muscle thickness of biceps brachii and triceps brachii

Changes in EMG amplitude

Time Frame: Changes from baseline at 5 and 10 weeks

Surface EMG

Changes in action potential amplitude

Time Frame: Changes from baseline at 5 and 10 weeks

Surface EMG Decomposition

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Joshua Carr

Assistant Professor

Texas Christian University

Study Sites (2)

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