Effect of Mindfulness Meditation on Physiological Response to Unpredictable Stimuli



Status:Active, not recruiting
Conditions:Anxiety, Healthy Studies, Psychiatric, Psychiatric, Psychiatric, Psychiatric
Therapuetic Areas:Psychiatry / Psychology, Other
Healthy:No
Age Range:18 - 65
Updated:8/23/2018
Start Date:June 20, 2017
End Date:July 25, 2021

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This study will evaluate the effects of Mindfulness-Based Stress Reduction (MBSR) on
physiological reactivity. This study will focus on individuals with anxiety who will
participate in an 8-week MBSR class. The investigators will test participants' reactivity to
both predictable and unpredictable stimuli before and after the class to understand the
physiological changes that may occur after to the intervention. Secondary measures include
psychometric instruments and a delay discounting task.

Mindfulness-Based Stress Reduction (MBSR) is a manualized, systematic training in mindfulness
meditation that has been found to have beneficial health effects, such as decreased stress
and anxiety. The current protocol aims to examine the effects of MBSR on several
physiological and behavioral measures in people with anxiety disorders, which may help us
understand the effects of the intervention on anxiety. The investigators will use the NPU
task as developed by the NIH, which measures an individual's response to threatening stimuli
(mild shock) paired with non-threatening stimuli (geometric shapes). Individuals with anxiety
disorders will be recruited to participate in this study, and will be randomized to a control
(waitlist) or MBSR intervention group. Other secondary measures will examine the effects of
mindfulness meditation on decision-making, and stress and anxiety symptoms.

Inclusion Criteria:

1. Men and women from 18-65 years of age.

2. Have an anxiety disorder, including: social anxiety disorder (SAD), generalized
anxiety disorder (GAD), panic disorder, posttraumatic stress disorder (PTSD),
agoraphobia, or simple phobia.

3. Must understand study procedure and willing to participate in 2 testing visits, and
MBSR course as assigned.

4. Participants must be able to give informed consent to the study procedures.

Exclusion Criteria:

1. Subjects experiencing a current depressive episode or other axis I psychiatric
disorders such as psychotic disorders, obsessive compulsive disorder, current eating
disorders, bipolar disorder, and current substance use disorders.

2. Lack of measurable eye blink/eye twitch response (3 times the baseline eye blink
muscle activity as measured by electromyography) for at least 5 of 9 startles used
during the habituation visit.

3. A serious medical condition that may result in surgery or hospitalization.

4. Subjects who will be non-compliant with the study procedures. This may include planned
travel out of town.

5. Women who are pregnant.

6. Current evidence of median nerve entrapment or carpal tunnel syndrome.

7. Subject who has resting blood pressure outside of a systolic blood pressure range of
90-140 mmHg, or a diastolic blood pressure outside a range of 50-90 mmHg on two
consecutive measurements, taken up to 10 minutes apart.

8. Subjects taking benzodiazepines, barbiturates, antidepressants, antipsychotics, or
sedative medications

9. Subjects currently receiving concomitant psychotherapy directed at treating anxiety
symptoms (i.e. CBT).

10. Individuals with implanted electronic devices, such as a cardiac pacemaker.

11. Individuals who have completed a full course of MBSR, an equivalent meditation
training, or have a daily meditation practice.
We found this trial at
1
site
3800 Reservoir Rd NW
Washington, District of Columbia 20007
(202) 687-7695
Phone: 202-687-0635
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