Effect of American Ginseng on Exercise-induced Muscle Soreness

NCT ID: NCT01827696

Last Updated: 2016-03-03

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

PHASE1

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-05-31

Study Completion Date

2013-12-31

Brief Summary

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Healthy participants will ingest American ginseng daily or a placebo for four weeks prior to engaging in a unaccustomed exercise bout designed to induce mild-moderate muscle soreness. Muscle soreness will be assessed via decrements in muscle strength and with a self-rating of perceived soreness before and several times after the exercise.

Detailed Description

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Healthy men and women will consume either 2000 mg of American ginseng daily (four 500 mg pills will be taken at four different times during the day always with food/meals) or a placebo (4 cellulose) for four weeks prior to engaging in a 40 minute downhill treadmill jog (12% decline) at a speed of 7 miles per hour. Participants will consume one pill with breakfast, one pill with lunch, one pill with dinner and another pill with a snack either between meals or prior to bedtime. The exercise will be consist of five, eight minute bouts of jogging with two minutes of rest/recovery in between. The degree of muscle soreness will be assessed using a Biodex strength testing machine (isometric and concentric isokinetic torque), and a self-rating of perceived soreness on a scale from zero to ten. All of the above measures will be taken before and several times after the downhill jogging protocol.

Conditions

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Muscle Damage

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Treatment

American Ginseng ingestion

Group Type EXPERIMENTAL

Ginseng

Intervention Type DIETARY_SUPPLEMENT

Effect of four weeks of daily Ginseng intake (2gm/day) on muscle soreness following downhill running exercise

Placeobo

non-active ingredient

Group Type PLACEBO_COMPARATOR

Ginseng

Intervention Type DIETARY_SUPPLEMENT

Effect of four weeks of daily Ginseng intake (2gm/day) on muscle soreness following downhill running exercise

Interventions

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Ginseng

Effect of four weeks of daily Ginseng intake (2gm/day) on muscle soreness following downhill running exercise

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Healthy men or women, (women must weigh between 55-65 kg., while men must weigh between 75-85kg).
* Participants must not have engaged in any endurance run training in the past 9 months.

Exclusion Criteria

* Injured
* Regular runners
* Pregnant (or with any chance they may become pregnant)
* Breast-feeding
* Diabetics or those taking medication for diabetes
* Insomniacs
* Schizophrenics
* Hyper- or hypotension
* Cancer
* Irregular heartbeats
* Heart disease
* Females with endometriosis or uterine fibroids
* Those who have surgery scheduled during the study or within the two weeks following the completion of the study
* Those taking warfarin or medication for depression.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

Sponsor Role lead

Responsible Party

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Peter Lemon

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Peter WR Lemon, PhD

Role: PRINCIPAL_INVESTIGATOR

Western University, Canada

Locations

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University of Western Ontario

London, Ontario, Canada

Site Status

Countries

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Canada

References

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Jung HL, Kwak HE, Kim SS, Kim YC, Lee CD, Byurn HK, Kang HY. Effects of Panax ginseng supplementation on muscle damage and inflammation after uphill treadmill running in humans. Am J Chin Med. 2011;39(3):441-50. doi: 10.1142/S0192415X11008944.

Reference Type BACKGROUND
PMID: 21598413 (View on PubMed)

Other Identifiers

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001

Identifier Type: -

Identifier Source: org_study_id

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