Clinical Trials Directory

Trials / Unknown

UnknownNCT00258492

Restless Legs Syndrome Exercise Intervention

The Prevalence and Outcomes of Restless Legs Syndrome Among Veterans - Exercise Intervention

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
30 (planned)
Sponsor
Northeastern Ohio Universities College of Medicine · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

A pilot study of an aerobic exercise intervention to moderate symptoms and improve sleep quality among patients with Restless Legs Syndrome (RLS). We, the researchers at Northeastern Ohio Universities College of Medicine, hypothesize that, relative to a control group, RLS sufferers who participate in an aerobic exercise intervention will demonstrate: 1. reduced RLS symptoms; 2. improved sleep quality; 3. reduced daytime sleepiness.

Detailed description

We will implement an exercise intervention among persons who suffer from RLS. Study members will be Veterans, over the age of 40, who have been identified as RLS cases as part of our larger study of "The Prevalence and Outcomes of Restless Legs Syndrome among Veterans." We will use a cross-over design in which Veterans will be randomly assigned to the exercise intervention or control. Each arm of the study will be 3 months duration. The protocol for the intervention will consist of twice weekly supervised exercise sessions. The goal for exercise participants will be to engage in continuous aerobic exercise for 45 minutes at an intensity of approximately 60% of VO2max. The control will be weekly support group meetings. Outcomes will be measured using standardized sleep scales, actigraphy, and daily sleep and exercise logs.

Conditions

Interventions

TypeNameDescription
BEHAVIORALAerobic exercise

Timeline

Start date
2005-12-01
Completion
2007-01-01
First posted
2005-11-24
Last updated
2007-01-26

Source: ClinicalTrials.gov record NCT00258492. Inclusion in this directory is not an endorsement.