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NCT07312357Toborzás még nem indult

Whole-Body Electrostimulation for Functional Recovery in Post-COVID Syndrome

Electrostimulation Suit as a Therapeutic Tool in Post-COVID Syndrome: Effects on Physical and Functional Status. A Randomized Controlled Trial

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. dec. 31.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

Post-COVID syndrome is a condition that affects some people after recovering from the acute phase of COVID-19. Common symptoms include persistent fatigue, reduced physical capacity, and difficulties performing everyday activities, which can significantly impact quality of life and independence. At present, there is limited scientific evidence on effective rehabilitation strategies for this population. The purpose of this study is to evaluate whether the use of a whole-body electrostimulation suit can improve fatigue, physical performance, and functional independence in people with post-COVID syndrome. Whole-body electrostimulation is a non-pharmacological technique that uses low-frequency electrical impulses to activate multiple muscle groups simultaneously and has shown potential benefits in other clinical populations. This is a randomized, double-blind, controlled pilot clinical trial. Participants will be randomly assigned to either an experimental group, which will receive active whole-body electrostimulation during functional activities, or a control group, which will follow the same sessions using the electrostimulation suit with minimal stimulation (placebo condition). Neither participants nor outcome assessors will know which group each participant belongs to. The intervention will consist of 12 supervised sessions conducted once per week. Outcomes will be assessed before and after the intervention, with an additional follow-up assessment three months later. The main outcomes include fatigue levels, functional capacity, physical performance, and independence in activities of daily living. Safety and tolerance to the intervention will be monitored throughout the study. The results of this study may help to determine the feasibility and potential effectiveness of whole-body electrostimulation as a rehabilitation tool for people with post-COVID syndrome and provide preliminary data for future larger-scale clinical trials.

Állapot (regiszter)
Toborzás még nem indult
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
30 (tervezett)
Első benyújtás
2025. dec. 16.
Kezdés
2026. márc.
Elsődleges befejezés
2026. szept.
Fő szponzor
Universidad Rey Juan Carlos
NCT-szám
NCT07312357

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 30
  • 2026. márc. és az elsődleges befejezés (2026. szept.) között
  • Nincs megadott helyszín, ország nélkül
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Use of anabolic drugs or medications that may interfere with muscle function.
  • Recent oncological surgery.

Más betegség

  • Presence of severe cardiovascular disease or uncontrolled medical conditions that contraindicate physical activity or electrostimulation.
  • Neurological disorders or severe neuromuscular diseases.
  • Epilepsy.
  • Active skin lesions or dermatological conditions in areas where electrodes are applied.
  • Acute venous thrombosis.
  • Presence of cardiac pacemakers or implanted electronic or conductive medical devices.
  • Any clinical deterioration or condition that, in the opinion of the investigators, would make participation unsafe.

Egyéb

  • Participation in other structured physical exercise or rehabilitation programs during the study period.
  • Pregnancy.
  • -

Kiket keres a vizsgálat

  • Diagnosis of post-COVID syndrome (long COVID), with persistent symptoms following SARS-CoV-2 infection.
  • Presence of fatigue and/or functional limitations associated with post-COVID syndrome.
  • Ability to understand the study procedures and provide written informed consent.
  • Ability to participate in the intervention and assessments according to the study protocol.
  • -

Életkor a regiszterben: 18 év – 70 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

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