Treatment for Psychogenic Disorders



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:April 2006
End Date:April 2009

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Treatment for Psychogenic Movement Disorders

This study will examine whether biofeedback treatment is effective in lessening or stopping
movement symptoms in people with psychogenic movement disorder. People with this condition
have increased or decreased movements that are not under their control and are not
associated with any know problem with the nervous system. Biofeedback is a type of therapy
that uses electronic instruments to monitor breathing and heart rate. This treatment has
been effective in patients with anxiety and panic attacks.

People 18 years of age and older diagnosed with psychogenic movement disorder may be
eligible for this study. Candidates are screened with a neurological history, physical
examination and psychiatric evaluation.

Participants come to the NIH Clinical Center for nine 1-hour test sessions over an 8-week
period for the following procedures:

Week 1 (two visits):

- Patients' movements are videotaped while they sit, stand and walk.

- Patients train on RESPeRATE device, a computerized musical biofeedback device to help
slow theirs breathing rate. The device has three components: a computerized module,
earphones, and a chest strap holding a breath sensor. The patients put the elastic
strap around their chest, put on the earphones, and sit in a chair. The device monitors
and analyzes their breathing to create a melody composed of two distinct tones - one
for inhalation and one for exhalation. Patients are instructed to match their breathing
to the tones, which gradually slow until they are breathing at a slower, therapeutic
rate.

- Patients' breathing is monitored and analyzed for information on breathing pattern and
rate.

- Patients complete questionnaires on level of relaxation before and after RESPeRATE
training.

- Patients take the RESPeRATE device home to use for two 10-minute practice sessions per
day. They complete relaxation questionnaires before and after each session.

Weeks 2-7:

- Patients' progress is monitored and reviewed from the previous week

- Patients' breathing is monitored and analyzed for information on breathing pattern and
rate.

- Patients complete questionnaires on level of relaxation before and after RESPeRATE
training.

- Patients are observed for 10 minutes while using the RESPeRATE device.

Week 8:

- Patients' progress is monitored and reviewed from the previous week

- Patients' breathing is monitored and analyzed for information on breathing pattern and
rate.

- Patients complete questionnaires on level o...

Objective:

To apply respiratory biofeedback to patients with Psychogenic Movement Disorders (PMD) with
a goal of decreasing involuntary movements.

Study Population:

Patients diagnosed with "clinically definite" PMD based on the Fahn-Williams scale

Design: Open-label pilot study

Outcome measures:

- To evaluate a possible decrease or resolution in involuntary movements caused by PMD as
measured by the Psychogenic Movement Disorder Scale. Videotaping will be performed pre-
and post-treatment and the videos will be evaluated by movement disorder specialists
who are blinded to the pre-treatment or post-treatment condition.

- To evaluate if respiratory biofeedback is an effective treatment for patients with PMD.

- To retrospectively evaluate the components of anxiety and depression with responders
versus non-responders.

- INCLUSION CRITERIA:

- Clinically definite functional (psychogenic) movement disorder as defined by Fahn and
Williams criteria diagnosed by a movement disorder neurologist.

- Patients who are at least 18 years old

- Able and willing to cooperate with the study requirements

EXCLUSION CRITERIA:

- Any underlying major medical or neurological conditions

- Patients whose movements are related to a known neurological disorder

- History of traumatic brain injury or history of strokes

- Current suicidal ideation

- Patients with a psychotic disorder

- Patients with active substance abuse within the last 6 months

- Patients with moderate to severe depression, Beck Depression Inventory (BDI) greater
than 18)

- Patients with any ongoing litigation related to their diagnosis of PMD.

- Patients with a definite overt stressor identified that is thought to be primarily
responsible for the PMD symptoms
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
?
mi
from
Bethesda, MD
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