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NCT00757796 Clinical Trial

Obstructive Sleep Apnea Syndrome and Attention Executive Function Disturbances

Obstructive Sleep Apnea Clinical Trial

Official title:
Obstructive Sleep Apnea Syndrome and Attention Executive Function Disturbances

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00757796
Other study ID # 143/06
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 21, 2008
Last updated September 21, 2008
Start date October 2008

Study information
Verified date September 2008
Source Assaf-Harofeh Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational

Clinical Trial Summary

Studies demonstrate that sleep disturbances are associated with cognitive dysfunction and attention deficit. However the correlation between the severity of obstructive sleep apnea and the degree of cognitive dysfunction was not demonstrated. Our hypothesis is that patients suffering from a more severe sleep apnea will demonstrate a greater degree of cognitive dysfunction.

Description:

Studies demonstrate that sleep disturbances are associated with cognitive dysfunction and attention deficit. However the correlation between the severity of sleep disturbances and the degree of cognitive dysfunction was not demonstrated.We intend to study 80 patients with various degrees of obstructive sleep apnea. All patients will undergo executive cognitive tests as well as tests to assess for levels of depression, anxiety and attention.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 80
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

1. Apnea hypopnea index>5

2. Age 20 - 70 years

Exclusion Criteria:

1. Pregnant women

2. Known chronic cardiovascular or pulmonary disease

3. Patients s/p CVA or brain damage

4. Known depression or other psychiatric disorder

5. Patients with severe cognitive dysfunction (MMSE<25)

6. Patients receiving stimulants, antipsychotic or anti-depression medications

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assaf-Harofeh Medical Center
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