Postural Tachycardia Syndrome Clinical Trial
Official title:
Relationship of Autonomic Function to Hypnotic Susceptibility
This study will investigate the relationship between susceptibility to hypnosis and
regulation of the autonomic nervous system (nerves that control involuntary body functions,
such as heart rate and sweating).
Hypnosis is a state of mind in which the individual is highly focused, relatively unaware of
his or her surroundings, and possibly more able to accept and use therapeutic suggestions.
People vary in their responsiveness, or susceptibility, while in hypnosis. People with
certain conditions, such as chronic fatigue syndrome (CFS), chronic pain, posttraumatic
stress disorder (PTSD), and generalized anxiety disorder (GAD) have altered hypnotic
susceptibility. Patients with chronic orthostatic intolerance (COI) often have symptoms
similar to those of individuals with CFS, chronic pain, PTSD, and GAD, and this study will
examine how patients with COI respond to hypnosis as compared with healthy normal
volunteers. COI is a group of disorders characterized by intolerance to prolonged standing.
Among them are neurocardiogenic syncope (NCS), in which patients have recurrent episodes of
sudden loss of consciousness, and postural tachycardia syndrome (POTS), in which patients
have a sustained increase in heart rate after standing.
In addition to the comparison of COI and normal volunteer responses to hypnosis, the study
will examine how hypnotic susceptibility is related to the ability to control autonomic
functions such as blood pressure, heart rate, and sweating. The autonomic nervous system is
activated when the body is stressed, not only from physical stimuli such as cold
temperature, but also from mental stimuli, such as seeing a rattlesnake up close. Hypnosis
may, therefore, be a useful tool to understand how the mind controls the autonomic nervous
system.
Healthy normal volunteers and patients with NCS or POTS who are 18 years of age or older may
be eligible for this two-part study. In part 1, participants complete a questionnaire and
are then tested for hypnotic susceptibility. For this test, a professionally trained
physician guides the subject through a procedure to achieve a hypnotic state. The subject is
asked to perform several simple tasks and is then guided back to a normal state of being. In
part 2, the subject undergoes hypnosis again, during which the physician offers various
suggestions while monitoring activity of the subject's autonomic nervous system. The subject
is connected to various sensors that continuously monitor blood pressure, heart rate, blood
flow, sweat response, skin electrical conduction, and brain wave activity. An intravenous
catheter is inserted into an arm vein to collect blood samples. At the end, the subject is
guided back to a normal state of being.
The hypnosis session in part 1 is videotaped in order to: 1) permit review by a scientist
who is unaware of the subject's condition and whose judgment will not, therefore, be biased;
and 2) have a record of the experimental data. Only qualified investigators will view the
videotape.
Status | Completed |
Enrollment | 93 |
Est. completion date | January 2006 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A and older |
Eligibility |
INCLUSION CRITERIA: Subjects are patients with COI (POTS or NCS) identified in existing diagnostic protocols of the Clinical Neurocardiology Section (CNCS) and age- and gender-matched healthy volunteers. Patients with COI must be evaluated first through these diagnostic protocols prior to being offered enrollment in this protocol. Participation in this protocol is offered to subjects independently of gender, race, ethnicity, religion, or creed. The studies in this protocol can be performed on an outpatient basis. Inpatients may also participate as long as participation does not interfere with the protocol(s) under which they have been admitted. EXCLUSION CRITERIA: Subjects are excluded based on: age less than 18 years, unwillingness to be hypnotized or videotaped; religious or other beliefs that would prevent engagement in hypnosis; psychosis or psychotic depression; non-fluency in spoken English; and inability to participate adequately in the tasks of the hypnotic susceptibility scale. In addition, patients are excluded if they are being treated with, and cannot discontinue, a drug likely to interfere with the scientific results. An example would be treatment with a beta-adrenoceptor blocker. Patients unable to discontinue nicotine or alcohol temporarily are excluded. Patients are not to discontinue any medications before the patient or the patient's doctor discusses this with the Principal Investigator, or the Research Nurse. If it is decided that discontinuing medications would be unsafe, then the patient is excluded from the study. Finally, subjects are excluded if there are technical limitations in placing an i.v. or monitoring devices. |
N/A
Country | Name | City | State |
---|---|---|---|
United States | National Institute of Neurological Disorders and Stroke (NINDS) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Accurso V, Winnicki M, Shamsuzzaman AS, Wenzel A, Johnson AK, Somers VK. Predisposition to vasovagal syncope in subjects with blood/injury phobia. Circulation. 2001 Aug 21;104(8):903-7. — View Citation
Goldstein DS, Holmes C, Frank SM, Naqibuddin M, Dendi R, Snader S, Calkins H. Sympathoadrenal imbalance before neurocardiogenic syncope. Am J Cardiol. 2003 Jan 1;91(1):53-8. — View Citation
Goldstein DS, Robertson D, Esler M, Straus SE, Eisenhofer G. Dysautonomias: clinical disorders of the autonomic nervous system. Ann Intern Med. 2002 Nov 5;137(9):753-63. Review. — View Citation
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