Activity and Balanced Eating to Reduce Comorbidities and Symptoms of MS
Stopped early · Not applicable
Conditions studied: Multiple Sclerosis
In brief
Multiple sclerosis (MS) is the leading cause of irreversible neurological disability among young women and the second leading cause of disability among young men in the U.S. Cardiometabolic risk factors including obesity and hyperlipidemia are common among people with MS, and these risk factors are associated with severity and frequency of MS relapses and disease progression. People with MS often experience symptoms of pain, fatigue, and depression, which make adhering to a healthy lifestyle difficult, as evidenced by the high rates of unhealthy behaviors including poor diet and physical inactivity among this group. Physical activity has reduced symptoms of MS and improved metabolic risk profiles, but little research has focused on the role of a dietary intervention combined with physical activity in this group. Therefore, the purpose of this study is to test the efficacy of a combined diet and physical activity intervention for reducing cardiometabolic risks and MS symptoms when compared to a physical activity intervention alone.
Key facts
- Study ID
- NCT03808545
- Run by
- University of Alabama at Birmingham
- People needed
- 11
- Starts
- 2019-02-26
- Expected to finish
- 2020-03-19
- Last updated by the study team
- 2022-11-18
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Relapsing-Remitting MS
- On disease modifying treatment for 6 months
- No relapse within the previous 30 days
- BMI 25-55 kg/m2
- Self-identify as not currently meeting recommendations for healthy diet and physical activity
- Ambulatory with or without assistance
- Reliable access to the internet via computer or smartphone
- Responsible for their personal food preparation or have input into the food prepared for them
- Score indicating low cognitive functioning on the Telephone Interview for Cognitive Status assessment
You may not qualify if…
- Physician does not approve participation
- Use of the following diabetes medications: Acetohexamide, Chlorpropamide (Diabinese), Tolbutamide (Orinase, Tol-Tab), Tolazamide (Tolinase), Glipizide (Glucotrol, Glucotrol XL, Metaglip), Glyburide (Micronase, DiaBeta, Glynase, Glucovance), Glimepiride (Amaryl), Humalog or lispro, Novolog or aspart, Apidra or glulisine, Regular (R) humulin or novolin, Velosulin (for use in the insulin pump), NPH (N), Lente (L), Ultralente (U), Lantus, Levemir or detemir, Humulin 70/30, Novolin 70/30, Novolog 70/30, Humulin 50/50, or Humalog mix 75/25
- Already on a specific diet meant to improve health
- Heart attack, stroke, or heart bypass surgery less than 6 months ago
- Pulmonary disease, cardiovascular disease or renal failure less than 6 months ago
- Smoking
- Cancer, HIV or liver/kidney disease
- Inability to travel to Lakeshore for testing
Where it is running
- Lakeshore Foundation — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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