Fatigue is the most common symptom of multiple sclerosis.
According to the National Multiple Sclerosis Society, an estimated of people living with multiple sclerosis (MS) experience fatigue.
Fatigue is also one of the most debilitating symptoms of MS, making it difficult for those people to maintain quality of life.
“MS fatigue can independently contribute to the disability that people with MS may experience,” Kathy Costello, associate vice president of healthcare access at the National MS Society, told Healthline. “MS fatigue stops people in their tracks. It is a feeling of mental or physical (or both) exhaustion that often comes on at the same time every day, is worsened by heat, is not related to physical activity or sleep, and prevents people from participating fully in their lives.”
Costello is also a nurse practitioner who sees MS patients at the Johns Hopkins Multiple Sclerosis Center.
“[Fatigue] can be immobilizing by interfering with relationships, work responsibilities, and social connections,” Costello said.
Possible new treatment
A variety of ways to help manage fatigue are available, but there is no effective treatment for it yet.
Ways to manage fatigue include occupational therapy, physical therapy, sleep regulation, heat management, psychotherapy, relaxation training, and stress management, as well as dopaminergic drugs and psychostimulants such as amantadine (Symmetrel) and modafinil (Provigil).
But a out of New York University is shedding light on the potential of a new form of help via electrical stimulation to the brain.
Transcranial direct current stimulation (tDCS) is a noninvasive way to deliver low direct current via electrodes on the head.
The research team developed a telerehabilitation protocol that delivers tDCS to participants at home using specially designed equipment and real-time supervision.
The tDCS device is portable and fits onto a person’s head.
This pilot study looked specifically at the feasibility of tDCS as a treatment for fatigue in people with MS.
The study followed 27 MS patients with varying levels of fatigue and wasn’t based on any specific symptoms.
Participants were randomly assigned in either a treatment or control group.
While it wasn’t a large trial, the results were significant.
Participants using tDCS experienced a significant reduction in fatigue levels.
“We are excited to see this benefit for fatigue that has no treatment,” , PhD, a lead study author and an associate professor of neurology and director of MS research at NYU Langone Health, told Healthline.
Participants evaluated themselves using a measurement scale known as the Patient-Reported Outcomes Measurement Information System (PROMIS) that grades fatigue on a score of up to 32, with the higher numbers meaning more fatigue.
After 20 sessions, all participants of fatigue to be lower.
But the group that underwent tDCS reported an average 5.6-point drop in fatigue while the placebo group only saw an increase of 0.9 points.
“The study affected me in a way I didn’t expect,” Diana Frustaci, a participant, told Healthline.
Frustaci didn’t know until the trial ended that she was in the control group, but she tried really hard at the games.
“I tried to improve my scores, which wasn’t even the point of the study, but that’s what I did anyway,” she said.
Frustaci explained how she experienced more fatigue after playing the games because she had to focus for 20 minutes straight but found that “it still improved my days, like I had done something positive, for myself and the study. Worked out my brain, and then my body, and it was like I was winning at life, even though I felt like a loser so often with MS.”
“The exact mechanism behind tDCS is unclear and requires more research,” added Charvet. “It is thought to stimulate the dorsolateral prefrontal cortex, allowing people to feel more alive and awake.”
In earlier studies, this part of the brain, when stimulated, to be more effective in fighting fatigue, helping Charvet and her team to focus their efforts on one location.
This pilot study was funded by the National MS Society and The Lourie Foundation Inc.
The findings further show that “an increased number of treatments work better. We just don’t know how much more,” Charvet said.
She added that she and the study’s co-authors will look at this and more in their next study.
Charvet plans to conduct larger clinical trials on tDCS for MS-related fatigue as well as motor skills and cognitive symptoms.
“We are hopeful to find funding for a large trial, which will create guidelines for clinical use. We know it can be a powerful therapy but [we’re] not sure how best to use it,” she said.
Editor’s note: Caroline Craven is a patient expert living with MS. Her award-winning blog is , and she can be found on .