Don't get left behind! The modernized ClinicalTrials.gov is coming. Check it out now.
Say goodbye to ClinicalTrials.gov!
The new site is coming soon - go to the modernized ClinicalTrials.gov
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Non-Invasive Optical Spectroscopic Methods for Dehydration Identification in Marathon Trainees

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01981902
Recruitment Status : Withdrawn (Not a clinical trial study)
First Posted : November 13, 2013
Last Update Posted : November 1, 2022
Sponsor:
Collaborator:
Beckman Laser Institute University of California Irvine
Information provided by (Responsible Party):
Beckman Laser Institute and Medical Center, University of California, Irvine

Brief Summary:
Dehydration can result from exposure to harsh environments including hot and dry desert climates. Soldiers and non-military workers are frequently required to work in hot, dry conditions, and dehydration can be productivity limiting and life threatening if unrecognized.

Condition or disease Intervention/treatment
Dehydration Device: Non-Invasive Optical Spectroscopic

Detailed Description:
The research can use low power laser technology to take measurements of muscle tissue water content in volunteers before and after marathon training runs to detect dehydration. Two slightly different devices can be used to detect dehydration. 1). diffuse optical spectroscopy and 2). spatial frequency domain imaging-modulated imaging The researchers can determined by use other methods to assess the level of dehydration status in runners. These methods will include taking weight and temperature before and after run, skin-fold measurements pre and post run, and obtaining saliva samples from before and after run. The researchers can determine the study use non-invasive, laser light technology measure tissue water concentrations, as an indicator of dehydration.

Layout table for study information
Study Type : Observational
Actual Enrollment : 0 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Non-Invasive Optical Spectroscopic Methods for Dehydration Identification in Marathon Trainees
Study Start Date : August 2013
Estimated Primary Completion Date : August 2018
Estimated Study Completion Date : August 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dehydration

Group/Cohort Intervention/treatment
Dehydration
Non-Invasive Optical Spectroscopic monitoring method for dehydration
Device: Non-Invasive Optical Spectroscopic
Non-Invasive Optical Spectroscopic




Primary Outcome Measures :
  1. Hydration [ Time Frame: up to 4 weeks ]
    Marathon Trainees



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Study population are the volunteers who are training for a marathon individually or under the guidance of the Leukemia Society Team in Training, the American Heart Association, or similar groups. These organizations run programs that include providing group-training situations for individuals interested in preparing for a marathon while participating in fund raising efforts.
Criteria

Inclusion Criteria:

  • male female ages of 18 and 60
  • training for a marathon

Exclusion Criteria:

  1. Poorly controlled diabetes mellitus
  2. Diabetes insipidus (excessive urination of water) as diagnosed by your physician
  3. disorder of the intestine
  4. Irritable bowel syndrome with excessive diarrhea, as diagnosed by a physician
  5. Congestive heart failure and subsequent use of a diuretic "water pill" to remove excess water from the body
  6. Have poor kidney function
  7. Have been diagnosed with hyperthyroidism/hypothyroidism by your physician

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01981902


Locations
Layout table for location information
United States, California
Beckman Laser Institute University of California Irvine
Irvine, California, United States, 92612
Sponsors and Collaborators
University of California, Irvine
Beckman Laser Institute University of California Irvine
Investigators
Layout table for investigator information
Principal Investigator: Matthew Brenner, MD Beckman Laser Institute
Layout table for additonal information
Responsible Party: Beckman Laser Institute and Medical Center, Matthew Brenner, M.D.,Department of Pulmonary and Critical Care Medicine, University of California, Irvine
ClinicalTrials.gov Identifier: NCT01981902    
Other Study ID Numbers: 20129075
First Posted: November 13, 2013    Key Record Dates
Last Update Posted: November 1, 2022
Last Verified: October 2022
Keywords provided by Beckman Laser Institute and Medical Center, University of California, Irvine:
Dehydration
Additional relevant MeSH terms:
Layout table for MeSH terms
Dehydration
Water-Electrolyte Imbalance
Metabolic Diseases
Pathologic Processes