Study Stopped
Not enough subjects have been recruited over an extended period.
Exploratory Study on the Timing of Multiple Sclerosis (MS) Symptoms
1 other identifier
observational
80
1 country
1
Brief Summary
The investigators' overall hypothesis is that appearance or worsening of relapsing-remitting multiple sclerosis (RR-MS) symptoms are affected by various factors including stress, hormonal cycles, illness and missed medications.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2008
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2008
CompletedFirst Submitted
Initial submission to the registry
June 10, 2009
CompletedFirst Posted
Study publicly available on registry
June 12, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2025
CompletedApril 15, 2026
April 1, 2026
16.8 years
June 10, 2009
April 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
number of days with appearance or worsening of symptoms
3 months
Secondary Outcomes (1)
timing of appearance or worsening of symptoms
3 months
Study Arms (1)
Relapsing-remitting multiple sclerosis
Females with relapsing-remitting multiple sclerosis
Eligibility Criteria
Females with relapsing-remitting multiple sclerosis, not menopausal, neither pregnant nor nursing, not treated with steroids in the last 30 days and not on experimental medications
You may qualify if:
- females
- diagnosed with relapsing-remitting multiple sclerosis
You may not qualify if:
- male
- no diagnosis of relapsing-remitting MS
- diagnosis of any other autoimmune disease or fibromyalgia
- peri-, post-, or surgically menopausal
- pregnant within past year or nursing
- history of chemotherapy
- on experimental medications
- treatment with steroids in the last 30 days
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Louisville (recruiting nationwide)
Louisville, Kentucky, 40292, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Cynthia Corbitt, PhD
University of Louisville, Dept. Biology
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
June 10, 2009
First Posted
June 12, 2009
Study Start
August 1, 2008
Primary Completion
May 1, 2025
Study Completion
May 1, 2025
Last Updated
April 15, 2026
Record last verified: 2026-04