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Clinical Trials/NCT06456502
NCT06456502
Recruiting
Not Applicable

Effectiveness of Non-invasive Neuromodulation Compared to Placebo on Sleep Quality in Patients With Post-COVID Symptoms: a Randomized Clinical Trial.

Universidad Rey Juan Carlos1 site in 1 country44 target enrollmentJune 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Long-COVID
Sponsor
Universidad Rey Juan Carlos
Enrollment
44
Locations
1
Primary Endpoint
Sleep quality
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Sleep quality and duration are critical to cognitive, emotional and physical well-being, and poor sleep quality has been associated with an increased risk of cognitive, psychological and cardiometabolic disorders. Several important physiological activities occur during sleep including a reduction in heart rate and blood pressure. In addition, sleep exerts important modulatory effects on hormone release. Previous studies have shown that lack of sleep can generate exaggerated cortisol responses or psychological and physiological stressors. Cortisol has widespread effects throughout the body and brain, affecting mood, arousal, energy, metabolic processes, and immune and inflammatory system functioning. Therefore, disruptions in cortisol secretion during the night can influence a wide variety of processes in our body that may contribute to the perception of poorer sleep quality. In addition, the salivary enzyme α-amylase is considered a biomarker of cognitive, psychosocial, emotional or physical stress. It is important to note that the autonomic nervous system (ANS) regulates several physiological processes, including heart rate, blood pressure, respiration, and digestion. The ANS consists primarily of the sympathetic system and the parasympathetic system. Increased parasympathetic activity is considered to promote health, whereas a dominant or overactive sympathetic branch is considered to be detrimental to health.

A recent study found that both sleep quality and quantity of sleep were associated with resting ANS functioning. They found that poorer sleep quality was associated with greater sympathetic dominance. Research on the sympathetic and parasympathetic branches of the ANS has shown that autonomic imbalances are precursors to disease formation and other health-related risks. Coronavirus disease 2019 (COVID-19), has in many cases involved the presence of long-lasting symptoms several weeks or months after surviving acute infection with the virus, leading to a new disease called long COVID-19 or post-COVID-19 syndrome (PCS). A recent study showed that sleep quality influences the relationship between symptoms associated with sensitization and mood disorders with health-related quality of life in people suffering from long COVID.

Non-invasive neuromodulation directed to ANS may be an option to treat the sleep disorders observed in patients with long COVID.

OBJETIVES:

Therefore, the primary objective of this study is to evaluate the efficacy of a treatment protocol on the ANS by means of non-invasive neuromodulation in aspects related to sleep in long COVID patients compared to placebo. As secondary objectives, we propose to evaluate the efficacy of a treatment protocol on the ANS by non-invasive neuromodulation in aspects related to ANS functioning, psychological variables, fatigue, pain perception and quality of life in patients with long COVID.

Registry
clinicaltrials.gov
Start Date
June 2024
End Date
June 30, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stella María Fuensalida Novo

Proffesor

Universidad Rey Juan Carlos

Eligibility Criteria

Inclusion Criteria

  • Subjects with long COVID or post- acute COVID syndrome
  • With a evolution of at least 6 months after acute SARS-cov-2 infection
  • Whit symptoms present at baseline.

Exclusion Criteria

  • Pregnancy.
  • Pacemakers
  • Ulcerations or wounds in the area of electrode application.
  • Decompensated heart disease.
  • Epilepsy and/or choreic syndromes.
  • Frequent medication with corticosteroids, hypnotics or supplements such as melatonin, Ashwagandha or phosphatidylserine.
  • Hypersensitivity on hands and feet that influence the use of the gloves and socks from the neuromodulation system.

Outcomes

Primary Outcomes

Sleep quality

Time Frame: Baseline, at the of 15th session, at 6 month an at one year

The aspects of sleep to be assessed by means of the Pittsburgh sleep quality index (PSQI) scale and the sleep diary to be completed each morning and handed in on the last day of treatment.

Secondary Outcomes

  • Cortisol and alpha amylase levels(Baseline and at 8 weeks)
  • Heart variability(Baseline and at 8 weeks)
  • Psychological variables(Baseline, at 8 weeks, at 6 month an at one year)
  • The quality of life(Baseline, at 8 weeks, at 6 month an at one year)
  • Disability(Baseline, at 8 weeks, at 6 month an at one year)
  • Pain intensity(Baseline, at 8 weeks, at 6 month an at one year)

Study Sites (1)

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