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Enhanced External Counterpulsation on Delayed Onset Muscle Soreness

NCT ID: NCT02175316

Last Updated: 2020-04-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-04-30

Study Completion Date

2017-09-06

Brief Summary

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This study will evaluate the effects of Enhanced External Counterpulsation on delayed onset muscle soreness. The primary outcomes will be duration of delayed onset muscle soreness, WBC count, CRP count, CPK count, and pain tolerance.

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Detailed Description

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Conditions

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Muscle Tightness

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Experimental: EECP for DOMS

All enrolled subjects will receive EECP treatment Delayed Onset Muscle Soreness.

Group Type EXPERIMENTAL

Enhanced External Counterpulsation

Intervention Type DEVICE

Enhanced External Counterpulsation

Interventions

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Enhanced External Counterpulsation

Enhanced External Counterpulsation

Intervention Type DEVICE

Other Intervention Names

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Lumenair Enhanced External Counterpulsation Therapy System, Vasomedical

Eligibility Criteria

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Inclusion Criteria

* Healthy active Duty or DoD beneficiaries between 25 and 59 years old

Exclusion Criteria

* Not on a physical profile
* Not taking any OTC or prescription pain medications or workout supplements
Minimum Eligible Age

25 Years

Maximum Eligible Age

59 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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David Grant U.S. Air Force Medical Center

FED

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sachin Shah

Role: PRINCIPAL_INVESTIGATOR

United States Air Force

Locations

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David Grant USAF Medical Center

Travis Air Force Base, California, United States

Site Status

Countries

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United States

Other Identifiers

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FDG20130045H

Identifier Type: -

Identifier Source: org_study_id

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