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NCT02077972 · ClinicalTrials.gov registry record · NA

Whole Body Hyperthermia & Combat-Related Posttraumatic Stress Disorder (PTSD)

A NA study, sponsored by University of Arizona.

Terminated
Registry status
NA
Development phase
3
Enrollment target

NCT02077972: Clinical Trial NA study, sponsored by University of Arizona.

NCT02077972 is a NA study that was terminated before completion, run by University of Arizona. The registered enrollment target is 3 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02077972, a NA study, was terminated before completion, sponsored by University of Arizona.

TERMINATED
Registry status
NA
Development phase
3 participants
Enrollment target

Study Summary

Combat-related post traumatic stress disorder (PTSD) has become an increasingly pressing public health problem in the United States following the overseas wars of the last decade. Rates of PTSD have skyrocketed in the military and among veterans, leading to increased rates of suicide, impairment on the job and off, and behavioral changes that negatively affect not just the veteran, but also his or her family. Although effective medication and psychotherapy treatments exist for combat-related PTSD, many individuals suffering with PTSD do not adequately respond to currently available treatment options, highlighting the need to develop and test new interventions for the disorder. To address this pressing clinical issue, the investigators will conduct a pilot study to determine if Whole Body Hyperthermia (WBH) reduces symptoms in adults suffering from combat-related PTSD. The investigators plan to recruit a sample of 10 medically healthy individuals with combat-related PTSD who will receive a single session of WBH to determine if this single session improves PTSD symptoms and, if so, whether this improvement will last at least 2 weeks. To do this, the study will include basic clinical and psychiatric assessments immediately before and one and four weeks after WBH. Because sleep is so often impaired in PTSD, the investigators will measure at-home sleep patterns for a week prior to and a week following the WBH session using sleep diaries and a wristwatch actigraphy device. Given scientific evidence from our research group that WBH may improve depression, the investigators anticipate that it may also be of benefit or adults suffering from combat-related PTSD.

Primary Outcome

Change in scores between baseline and subsequent assessments will be assessed to determine the effect of WBH on PTSD symptoms.

Interventions

  • DEVICE High intensity whole-body infrared heating

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2014-03
Est. Completion 2016-02
Phase NA
University of Arizona

349 total trials

Why NCT02077972 stopped before completion

NCT02077972 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which High intensity whole-body infrared heating is the first listed.

NCT02077972 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02077972 about?

NCT02077972 is a clinical study titled "Whole Body Hyperthermia & Combat-Related Posttraumatic Stress Disorder (PTSD)". Combat-related post traumatic stress disorder (PTSD) has become an increasingly pressing public health problem in the United States following the overseas wars of the last decade. Rates of PTSD have skyrocketed in the military and among veterans, leading to increased rates of suicide, impairment on ...

What is the current status of trial NCT02077972?

This trial is currently terminated. It is a NA study. The enrollment target is 3 participants. The study started on 2014-03. Estimated completion is 2016-02.

What interventions are being tested in trial NCT02077972?

The interventions under investigation include: High intensity whole-body infrared heating (DEVICE).

Who is sponsoring clinical trial NCT02077972?

This trial is sponsored by University of Arizona, which has 349 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02077972's enrollment target sits among peer trials

3 1996th of 2000 higher than 4 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02077972, the US trial registry maintained by the National Library of Medicine. NCT02077972 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.