Sleep Disturbance and Sleep Quality in Women With Fibromyalgia Syndrome
This study is currently recruiting patients.
Verified by University of Kentucky June 2007
| Sponsored by: |
University of Kentucky |
| Information provided by: |
University of Kentucky |
| ClinicalTrials.gov Identifier: |
NCT00482859 |
|
Purpose
The purpose of this week long study is to describe sleep and problems with sleep in women diagnosed with Fibromyalgia syndrome.
| Condition |
Fibromyalgia Syndrome
|
MedlinePlus
related topics:
Fibromyalgia
Study Type: Observational
Study Design: Natural History, Longitudinal, Defined Population, Prospective Study
Official Title: Sleep Disturbance and Sleep Quality in Women With Fibromyalgia Syndrome
Further study details as provided by University of Kentucky:
Total Enrollment: 50
Study start: April 2007; Expected completion: April 2008
At least 50 women over 18 years of age are invited to volunteer in this study conducted in Kentucky. Sleep quality and problems with sleep will be described using several kinds of measures. Questionnaires on sleep and Fibromyalgia will be completed by the volunteer. In addition, the volunteer will complete a sleep diary for at least 7 days and wear an Actiwatch (a wrist watch like device that measures sleep).
Participants may not be in the study if they work night shift (11 pm - 7 am) or have been diagnosed with a condition called sleep apnea.
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Female
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
-
Women 18 years old; diagnosed with Fibromyalgia;
Exclusion Criteria:
-
Volunteer works night shift (11PM - 7AM);
-
Volunteer has been diagnosed with sleep apnea.
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00482859
United States, Kentucky
Office of Suzette Sewell, Louisville, Kentucky, 40213, United States; Recruiting
University of Kentucky, Lexington, Kentucky, 40509, United States; Recruiting
Study chairs or principal investigators
Suzette L Sewell, RN MSN, Principal Investigator, University of Kentucky
More Information
IRB approved flyer posted
Study ID Numbers: 07-0188-P2G
Last Updated: June 4, 2007
Record first received: June 3, 2007
ClinicalTrials.gov Identifier:
NCT00482859
Health Authority: United States: Institutional Review Board
