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CompletedNCT01450852Updated Oct 12, 2011

Strength Training Induced Alterations in Markers of Immune Function

An interventional study of Strength Training in Inflammation, sponsored by Louisiana State University Health Sciences Center in New Orleans. Completed at 1 site in United States. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-10-12.

Sponsored by Louisiana State University Health Sciences Center in New Orleans · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Non-randomized
Ages
18 Years to 30 Years
Sex
All
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Study summary

Exercise has been used to help prevent or slow the progression of inflammation-related disease; however, the mechanism by which this activity may lower concentrations of inflammatory markers remains unclear. The melanocortin receptors 1,3 and 5 (MC1R, MC3R and MC5R) have been shown to function in an anti-inflammatory manner and have the potential to mediate the positive immune adaptations associated with regular physical activity.

Preliminary data suggest that MC3R gene expression increases in whole blood after chronic exercise training. The primary aim of the current study is to explore whether this change in gene expression translates into alterations in MC1R, MC3R, or MC5R monocyte surface expression. The secondary aim is to examine the relationship between surface expression of these receptors and circulating inflammatory profiles.

The investigators will recruit 42 untrained, healthy males and females aged 18-35 yrs. Half of the group will be placed on an exercise program for 15 weeks. The other half will serve as untrained control subjects. In addition to basic anthropometric measures, the investigators will measure concentrations of inflammatory and anti-inflammatory cytokines (ELISA) and cell surface expression of MC1R, MC3R, and MC5R on monocytes (flow cytometry).

Read the detailed description

Abstract:

Chronic exercise reduces inflammation, but the mechanisms involved are unclear. Recent studies have shown that stimulation of melanocortin 1 and 3 receptors (MC1R and MC3R) on immune cells increases anti-inflammatory cytokine production. PURPOSE: To examine the influence of 12 weeks of resistance training (RT) on body composition, monocyte cell-surface expression of MC1R and MC3R and circulating markers of inflammation. METHODS: Healthy, active males and females (age 20-27 yr) were recruited into a RT group (RE; n = 23) and an active control group (AC; n = 19). RE completed 12 weeks of progressive, periodized RT 3d/wk while AC maintained normal activity habits. Measures of body composition (DXA) were taken and blood was collected prior to (PRE) and following the intervention period (POST). Blood samples were analyzed for monocyte cell-surface expression MC1R, MC3R, MC5R and C-reactive protein (CRP) and the plasma cytokines interleukin 6 (IL-6) and interleukin 10 (IL-10) using flow cytometry and ELISAs respectively.

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Conditions studied

  • Inflammation

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Keywords

  • Melanocortin Receptor
  • Monocyte
  • Resistance Training
  • Inflammation
  • Markers of Inflammation
03

In context

Inflammation

3,439 studies on the registry are indexed under Inflammation; 629 are open to participants now.

This study's enrollment of 42 is below the median of 50 across 2,437 interventional studies indexed under Inflammation.

Browse Inflammation studies →

Lead sponsor

Louisiana State University Health Sciences Center in New Orleans is the lead sponsor of 70 studies on the registry; 12 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 1 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • All Participants Must be Healthy
  • The Strength Training Group Members Must Be Approved For Participation by a Licensed MD

Exclusion criteria

Exclusion Criteria:

  • Females may not be pregnant
  • Unhealthy participants (those with existing conditions)
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
42 participants (actual)

Study arms

  • Experimental
    Strength Training

    The strength training group completed 12 weeks of progressive, periodized resistance training 3d/wk.

    Behavioral: Strength Training

  • No intervention
    Active Control Group

    The active control group was instructed to maintain normal activity and eating habits. They participated in all pre and post intervention measures.

Interventions

  • BehavioralStrength Training

    Each Member of this group completed 12 weeks of progressive, periodized resistance training for 3d/wk.

06

What researchers measure

Primary outcomes

  1. Melanocortin 1 Receptor Expression on Monocytes

    Blood samples were analyzed for monocyte cell-surface expression of the melanocortin 1 receptor using flow cytometry. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After 12 Week of Intervention Period

  2. Plasma CRP

    Blood samples were analyzed for C-reactive protein using ELISA. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After the 12 Week Intervention Period

  3. Body Composition (Fat Tissue Amount)

    Body composition was assessed using DXA. Pre measures were completed in Jan. 2010 and post measures were completed in May 2010 for all subjects.

    Time frame: Before and After the 12 Week Intervention Period

  4. Plasma IL-6

    Blood samples were analyzed for IL-6 using ELISA. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After the 12 Week Intervention Period

  5. Plasma IL-10

    Blood samples were analyzed for IL-10 using ELISA. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After the 12 Week Intervention Period

  6. Melanocortin 3 Receptor Cell Surface Expression on Monocytes

    Blood samples were analyzed for monocyte cell-surface expression of the melanocortin 3 receptor using flow cytometry. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After the 12 Week Intervention Period

  7. Melanocortin 5 Receptor Cell Surface Expression on Monocytes

    Blood samples were analyzed for monocyte cell-surface expression of the melanocortin 5 receptor using flow cytometry. Pre samples were collected in Jan. 2010 and post samples were collected in May 2010 from all subjects.

    Time frame: Before and After the 12 Week Intevention Period

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Study locations

1 site
  • Louisiana State University
    Baton Rouge, Louisiana 70803, United States
08

References and documents

Publications

  • Henagan TM, Forney L, Dietrich MA, Harrell BR, Stewart LK. Melanocortin receptor expression is associated with reduced CRP in response to resistance training. J Appl Physiol (1985). 2012 Aug;113(3):393-400. doi: 10.1152/japplphysiol.00107.2012. Epub 2012 Jun 7. PubMed 22678961 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01450852
Lead sponsor
Louisiana State University Health Sciences Center in New Orleans
Responsible party
Laura Stewart (Assistant Professor, Louisiana State University Health Sciences Center in New Orleans) — Principal investigator
First posted
Oct 12, 2011
Start date
Jan 2010
Primary completion
May 2010
Completion
May 2010
Last update
Oct 12, 2011

Study contacts

Laura K Stewart, PhD
principal investigator · Louisiana State University Health Sciences Center in New Orleans

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2011. You cannot join it, but the record below documents what was studied.

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