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OpenTrials
Completed

NCT Number: NCT00482859

Sleep Disturbance and Sleep Quality in Women With Fibromyalgia Syndrome

The purpose of this week long study is to describe sleep and problems with sleep in women diagnosed with Fibromyalgia syndrome.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

About this study

At least 50 women over 18 years of age are invited to volunteer in this study. 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). At completion of the study, participants will be provided a print out of their sleep obtained from the Actiwatch.

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.

Participants need not live in Kentucky to participate in this study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women 18 years old; diagnosed with Fibromyalgia;

Exclusion criteria

  • Volunteer works night shift (11PM - 7AM);
  • Volunteer has been diagnosed with sleep apnea.

Sponsors and collaborators

Lead sponsor

University of Kentucky

Other

Registry information

Important dates

Study start
2007
Primary completion
2007
Study completion
2008
First posted
Jun 5, 2007
Registry last updated
Jan 22, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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