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Fort Hood, Texas Clinical Trials

A listing of Fort Hood, Texas clinical trials actively recruiting patient volunteers.

RESULTS

Found (9) clinical trials

Sleep Disturbance in Deployed Soldiers

Hypotheses: - Hypothesis 1 - Sleep can be measured in Theater using actigraph technology. - Hypothesis 2 - Standard sleep measures in Soldiers randomized to a sleep intervention group will more closely approximate normal as compared to sleep measures of Soldiers randomized to the control group.

Phase

4.62 miles

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

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.

Phase N/A

4.62 miles

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Treatment of Comorbid Sleep Disorders and Post Traumatic Stress Disorder (PTSD)

The primary objective of the current study is to determine if providing cognitive-behavioral therapy of Insomnia and nightmares (CBTin) and Cognitive Processing Therapy of PTSD (CPT) results in greater PTSD and sleep symptom reduction than CPT only. A secondary objective is to determine if the sequencing of CBTl&N before or ...

Phase N/A

4.62 miles

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Randomized Evaluation of Octreotide Versus Compazine for Emergency Department Treatment of Migraine Headache

A urine pregnancy test will be performed on women of child bearing age. After informed consent is obtained, each patient will be placed in a dark private room and asked to grade nausea, pain, and sedation on a 10 cm visual analog scale, using the left end as the zero ...

Phase

4.62 miles

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Strong Families Strong Forces: Supporting Active Duty Families With Very Young Children

The overall aim of this research is to adapt and evaluate the efficacy of a parenting program compared to a parental self-care program for Active Duty families. A sample of 150 Active Duty families with young children who have a parent scheduled to deploy in the next six months will ...

Phase N/A

4.62 miles

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Variable-length Cognitive Processing Therapy for Combat-Related PTSD

The primary goal of this study is to improve the overall efficacy of cognitive processing therapy-cognitive-only version (CPT-C) in a sample of 130 active-duty service members through a variable length treatment. The study seeks to determine if some service members would benefit from a longer or shorter dose of treatment ...

Phase N/A

4.62 miles

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Evaluation of a Self-Care Toolkit in Surgical Breast Cancer Patients

The main research questions focus on whether the toolkit provides short-term benefits on symptoms associated with surgery (i.e., pain, anxiety, nausea) and whether it impacts emotional distress and other symptoms (i.e., pain, fatigue, sleep disturbance, global health, quality of life) at a two-week post-operative time point. This study will be ...

Phase N/A

4.62 miles

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Predictors of Treatment Response to Fluoxetine in PTSD Following a Recent History of War Zone Stress Exposure

While most soldiers exposed to the stresses of the war-zone exhibit psychological resilience, about one-fifth become psychological casualties of war. The fact that such a significant number of soldiers have difficulty adapting to life after war exposure suggests that we need to have well-defined treatments that are effective and cost-efficient. ...

Phase

4.65 miles

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Study of Fluticasone Propionate Multidose Dry Powder Inhaler Compared With Fluticasone Propionate/Salmeterol Multidose Dry Powder Inhaler

This study is to evaluate the safety and efficacy of Fluticasone Propionate and Fluticasone propionate Salmeterol in pediatric patients with a documented history of persistent asthma.

Phase

5.44 miles

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