Observational Study for Multiple System Atrophy (MSA) at UT Southwestern
This is an observational study looking at how Multiple System Atrophy (MSA) affects people and how multidisciplinary care (care from a team of different specialists) impacts your quality of life and the burden on your caregivers. You could join if you are 18 or older, have possible or probable MSA, and are a patient at the UT Southwestern MSA clinic, able to attend clinic every four months. The study will measure your quality of life related to MSA over five years to see the impact of this care. The current recruitment status is unclear.
- Study design
- This is an observational study planning to include 200 participants. It is a prospective cohort study, meaning participants are followed over time.
- What's involved
- You and your caregivers would attend a multidisciplinary MSA clinic every four months. You would also complete online and paper questionnaires at home or in the clinic.
- Compensation
- Not stated in the trial record.
- Follow-up
- You will be contacted for follow-up information for up to five years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Multiple System Atrophy Multidisciplinary Clinic
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Steven Vernino, M.D. · PRINCIPAL_INVESTIGATOR · University of Texas Southwestern Medical Center
Who to contact
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Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Multiple System Atrophy-Quality of Life (MSA-QoL)at 5 year evaluation
The disease burden of MSA and impact of multidisciplinary care on the quality of life of patients as measured by the MSA-Quality of Life (QOL) questionnaire completed every four months by the patients. The scale measures how MSA affects a person's quality of life in day to day activities. The scale ranges from No problem to Extreme Problem. The More Extreme Problem sections selected the more their quality of life is affected by the disease.