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Water Immersion for PTSD
N/A
Waitlist Available
Led By Rebecca Benfield, PhD
Research Sponsored by University of Nevada, Las Vegas
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately following immersion
Awards & highlights
No Placebo-Only Group
Summary
This trial explores the effects of warm water immersion on student Veterans with PTSD, depression, anxiety, and pain. The warm water is thought to help by calming the body and mind, making participants feel more relaxed and less stressed.
Who is the study for?
This trial is for student veterans enrolled at UNLV who can get in and out of a pool without help, have served in the military, and currently have PTSD symptoms. It's not for those with traumatic brain injury, fear of water, heart/lung disease, diabetes, severe mental illness (except depression), extreme obesity, open wounds or missing lower limbs.
What is being tested?
The study tests the effects of warm water immersion on PTSD symptoms among these students. Participants will be immersed to chest level to assess changes in their physical and psychological state including any impacts on associated depression, anxiety and pain.
What are the potential side effects?
While specific side effects are not listed for warm water immersion therapy itself; potential risks may include discomfort due to prolonged exposure to warmth or exacerbation of certain pre-existing conditions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre immersion baseline (dry) immersion at 15 minutes (wet) and 45 minutes (wet)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre immersion baseline (dry) immersion at 15 minutes (wet) and 45 minutes (wet)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Multidimensional Mood State Questionnaire (MDMQ) Change is being assessed
Salivary Alpha-Amylase change is being assessed
Semi-structured interview
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: ImmersionExperimental Treatment1 Intervention
This group will receive the immersion intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for PTSD include psychological therapies like Cognitive Behavioral Therapy (CBT) and Exposure Therapy, which work by changing thought patterns and reducing avoidance behaviors through controlled exposure to trauma-related stimuli. Pharmacological treatments, such as SSRIs, target neurotransmitter systems to alleviate symptoms of anxiety and depression.
The warm water immersion study suggests that thermal and hydrostatic effects can promote relaxation and reduce stress, offering a non-invasive, soothing treatment option that may complement traditional therapies. This is important for PTSD patients as it provides additional avenues for symptom relief and overall well-being.
Theoretical and empirical issues in the treatment of post-traumatic stress disorder in Vietnam veterans.Differentiation of pain ratings in combat-related posttraumatic stress disorder.
Theoretical and empirical issues in the treatment of post-traumatic stress disorder in Vietnam veterans.Differentiation of pain ratings in combat-related posttraumatic stress disorder.
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Who is running the clinical trial?
University of Nevada, Las VegasLead Sponsor
73 Previous Clinical Trials
14,025 Total Patients Enrolled
Rebecca Benfield, PhDPrincipal InvestigatorUniversity of Nevada, Las Vegas
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are currently experiencing symptoms of PTSD.You have served in the military before, according to your own report.You currently have heart or lung problems and have reported them yourself.You have diabetes.You have severe obesity that may affect your participation in the trial.You are currently taking medication for depression, pain or inflammation, including over-the-counter pain relievers.You have experienced a head injury.You are afraid of water.You have been diagnosed with a mental illness, except for depression as a secondary diagnosis.You have an open wound.You are missing one or both legs below the knee.
Research Study Groups:
This trial has the following groups:- Group 1: Immersion
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.