Myalgic encephalomyelitis Nervous System Diseases
Conditions
Interventions
Following obtaining informed consent, due to the energy limitations of the participants, the information sheet and Fatigue Severity scale (FSS) will be sent ahead of time so the participants can read
Sponsors
University of Leicester
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: People with myalgic encephalomyelitis and healthy controls
Exclusion criteria
Exclusion criteria: 1. Below the age of 18 years 2. People with very severe ME
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VO2 and respiratory exchange ratio measured using a portable metabolic system at a single timepoint | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Heart rate variability using a firstbeat device measured on the day of testing and for up to 5/6 days afterwards 2. Lactic acid using a COSMED device - lactate pro 2 measured on the day of testing and for up to 5/6 days afterwards 3. BP, HR, O2 saturations, Blood Pressure measured using a digital sphygmomanometer, Heart Rate and Oxygen saturations measured using a pulse oximeter, on the day of testing and for up to 5/6 days afterwards 4. Accelerometry using an actigraph device which measures activity levels for up to 5/6 days afterwards | — |
Countries
England, United Kingdom
Outcome results
None listed