Proteomic Response to Exercise in Adults With Restless Legs Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn how exercise changes molecules in the blood in people with restless legs syndrome (RLS) to better understand the cause(s) of RLS. The main questions the investigators aim to answer are: How does long-term exercise change proteins in the blood? How does a single exercise session change proteins in the blood? The investigators will compare long-term exercise to no exercise to see if the changes in proteins are specific to exercise. Participants will complete an exercise test and provide blood samples before and after the exercise test. Participants will be randomized (like the flip of a coin) in to either the exercise or no-exercise group for 12 weeks and then complete the exercise test and blood samples again at the end.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• age 18 years or older;

• diagnosis of RLS;

• presence of moderate-to-severe RLS (IRLS score\>15);

• currently untreated RLS;

• being non-active defined as not engaging in regular activity (30 minutes accumulated per day) on more than 2 days of the week during the previous six months;

• ability to walk without assistance (does not use a cane/walker/wheelchair for mobility;

• willing to complete outcome measures and complete the exercise program

Locations
United States
California
Stanford University
RECRUITING
Stanford
Contact Information
Primary
Katie Cederberg, PhD
kcederb@stanford.edu
(650) 725-6517
Time Frame
Start Date: 2024-10-21
Estimated Completion Date: 2026-12
Participants
Target number of participants: 30
Treatments
Experimental: Exercise
Participants will complete a 12-week, RLS specific exercise program including strength training, cardiovascular exercise, and stretching.
No_intervention: Non-Exercise
Participants will have no intervention or interaction for 12 weeks.
Related Therapeutic Areas
Sponsors
Leads: Stanford University

This content was sourced from clinicaltrials.gov