Clinical Trials Directory

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UnknownNCT00866411

Cranial Electrotherapy Stimulation (CES) for Soldiers With Combat-Related Symptoms

Outcomes of Cranial Electrotherapy Stimulation (CES) With Soldiers for Combat-Related Symptoms

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Brooke Army Medical Center · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this double-blind randomized control research study is to determine if CES given in a group setting for soldiers experiencing irritability is effective to reduce the symptom of irritability.

Conditions

Interventions

TypeNameDescription
PROCEDUREcranial electrotherapy stimulation (CES) with Alpha-Stimthree weeks of the cranial electrotherapy stimulation (CES) treatment (15 sessions of 60 minute treatments)
PROCEDUREplacebothree weeks of placebo treatment via a double-blinded procedure so that neither the Soldier nor the study investigators will know whether the Soldier is receiving the actual treatment or placebo

Timeline

Start date
2007-05-01
Primary completion
2009-05-01
Completion
2010-01-01
First posted
2009-03-20
Last updated
2009-03-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00866411. Inclusion in this directory is not an endorsement.