Transcutaneous electrical nerve stimulation for fibromyalgia-like syndrome in patients with Long-COVID: a pilot randomized clinical trial.

Publication date: Nov 08, 2024

This study investigated the effect of Transcutaneous Electrical Nerve Stimulation (TENS) for fibromyalgia-like symptoms including chronic widespread musculoskeletal pain, fatigue, and/or gait impairment in twenty-five individuals with long-COVID. Participants were randomized to a high dose (intervention group, IG) or low dose (placebo group, PG) TENS device. Both groups received daily 3-5 h of TENS therapy for 4-weeks. The Brief Pain Inventory assessed functional interference from pain (BPI-I), and pain severity (BPI-S). The global fatigue index (GFI) assessed functional interference from fatigue. Wearable technology measured gait parameters during three 30-feet consecutive walking tasks. At 4-weeks, the IG exhibited a greater decrease in BPI-I compared to the PG (mean difference = 2. 61, p = 0. 008), and improved in gait parameters including stride time (4-8%, test condition dependent), cadence (4-10%, depending on condition), and double-support phase (12% in dual-task) when compared to baseline. A sub-group meeting the 2010 American College of Rheumatology Fibromyalgia diagnostic criteria undergoing high-dose TENS showed GFI improvement at 4-weeks from baseline (mean change = 6. 08, p = 0. 005). Daily TENS therapy showed potential in reducing functional interference from pain, fatigue, and gait alterations in long-COVID individuals. The study’s limited power could affect the confirmation of certain observations. Extending the intervention period may improve treatment effectiveness.

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Concepts Keywords
2010american Adult
Daily Aged
Fibromyalgia COVID-19
Pilot Fatigue
Randomized Female
Fibromyalgia
Gait
Humans
Male
Middle Aged
Pilot Projects
SARS-CoV-2
Treatment Outcome

Semantics

Type Source Name
disease MESH fibromyalgia
disease MESH syndrome
disease MESH musculoskeletal pain
disease MESH gait
disease IDO intervention
disease MESH Long COVID
disease MESH Sequelae
disease MESH COVID 19
disease MESH central sensitization
disease MESH neuroinflammation
drug DRUGBANK Coenzyme M
disease MESH infection
disease MESH neuromuscular diseases
disease MESH Myasthenia Gravis
disease MESH multiple sclerosis
drug DRUGBANK Albendazole
disease MESH lifestyle
disease IDO facility
drug DRUGBANK Aspartame
drug DRUGBANK Methionine
disease IDO history
disease MESH osteoarthritis
drug DRUGBANK Pregabalin
disease MESH High blood pressure
disease MESH Depression
disease MESH Brain fog
drug DRUGBANK Oxygen
disease MESH Insomnia
disease MESH Unsteady gait
disease MESH Atrophy
disease MESH Numbness
disease MESH chronic pain
disease MESH stroke
drug DRUGBANK Duloxetine
disease MESH physical inactivity
disease MESH inflammation
disease MESH Anemia
disease MESH Arthritis
disease MESH death
disease MESH abnormalities
disease MESH cognitive dysfunction
disease IDO site
drug DRUGBANK Isoxaflutole
disease MESH peripheral neuropathy
disease MESH scar
disease IDO symptom
disease MESH major depressive disorder
drug DRUGBANK Milnacipran
disease MESH AIDS
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH anxiety
disease MESH relapse
disease MESH minimal clinically important difference
disease MESH Functional status
pathway REACTOME Reproduction

Original Article

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