Postural Tachycardia Syndrome Clinical Trial
Official title:
Origins of Cognitive Dysfunction in Postural Tachycardia Syndrome (POTS)
Verified date | August 2016 |
Source | Vanderbilt University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
A common complaint among people with Postural Tachycardia Syndrome (POTS) is "brain fog" or difficulty concentrating. This is very poorly understood. To better understand this cognitive dysfunction, the investigators will test people with POTS and people without POTS using various neuropsychiatric instruments. The investigators hypothesis is that people with POTS will have greater abnormalities on neuropsychiatric testing than normal controls.
Status | Completed |
Enrollment | 60 |
Est. completion date | June 2015 |
Est. primary completion date | June 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: All - Ages between 18-60 years - Male and female subjects are eligible - Able and willing to provide informed consent POTS - additional inclusion criteria - Diagnosed with postural tachycardia syndrome by Vanderbilt Autonomic Dysfunction Center (increase in heart rate greater than or equal to 30 beats per minute with position change from supine to standing (10 minutes; chronic symptoms consistent with POTS that are worse when upright and get better with recumbence.) Control subjects - additional inclusion criteria - Gender matched to POTS patients - Age-matched to POTS patients (+/- 5 years of a POTS patient) - Grossly matched in intelligence to POTS patients Exclusion Criteria: ALL - Inability to give or withdrawal of informed consent - Pregnancy (determined by patient self report) - Other factors which in the investigator's opinion would prevent the subject from completing the protocol. POTS - additional exclusion criteria - Overt cause for postural tachycardia (such as acute dehydration) Normal Controls - additional exclusion criteria - Previously diagnosed with Axis I psychiatric disorder - Previously diagnosed learning disorder - Previously diagnosed attention deficit hyperactivity disorder (ADHD) - Prior psychosis - past or present substance abuse - History of loss of consciousness - History of seizures |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt University | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University |
United States,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Standing Digits Backwards Test | This is a continuous variable that will provide a measure of attention with orthostatic stress. | In the standing position for approximately 15 minutes. This is a cross-sectional study with no follow-up. | No |
Secondary | Cognitive Domain Score (CDS) | The CDS will consist of 1: Seated memory (Randt Short Story subtes, Paired words subtes and Digits Forward) and standing memory (Randt short story, paired words and digits forward). 2. Seated Complex Attention (Ruff, SDMT, Trails A, Randt, Digits Backward) and standing complex attention (Randt digits backward) 3. Executive functioning only while standing (Stroop, Trails) 4. Seated and standing verbal fluency (COWA). |
At seated and standing. This is a cross-sectional study without follow-up. All assessments are performed on a single day. | No |
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