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More info
You can access this
clinical trial
if you have
Stress, Physiological or Stress, Psychological
and you are
between 18 and 50
years old
-
The phase for this study is not defined.
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The purpose

The primary purpose of the present study is to investigate the relationship between mindfulness and stress habituation. The investigators propose to measure the effect of mindfulness on stress habituation by randomly assigning participants to a 6-week mindfulness-based stress reduction group intervention, a cognitive-behavioral skills group comparison intervention, or a waitlist control condition followed by repeated acute psychosocial stress testing (2 laboratory sessions on 2 separate days). Saliva will be collected from participants throughout both laboratory testing sessions to measure HPA axis activation (an essential stress-responsive system), along with other measures of physiological and psychological stress (e.g., heart rate, blood pressure, emotions). Mediators and moderators of treatment outcome will be examined. The cognitive-behavioral skills group condition is an appropriate comparison group due to the well-documented efficacy of cognitive-behavioral interventions on stress.

Provided treatments

  • Behavioral: Mindfulness Based Stress Reduction
  • Behavioral: Cognitive-Behavioral Therapy (CBT) Group

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02894229. The sponsor of the trial is Ohio University and it is looking for 150 volunteers for the current phase.
Official trial title:
The Mindfulness Intervention and Repeated Acute Stress (MIRAS) Study