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Electric suit trial aims to jolt long COVID fatigue away

NCT ID NCT07312357

Symptom relief Sponsor: Universidad Rey Juan Carlos Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a whole-body electrostimulation suit can reduce fatigue and improve physical function in people with Long COVID. 30 adults with persistent symptoms will be randomly assigned to receive either active stimulation or a placebo version during 12 weekly sessions. The goal is to see if this non-drug approach can help with daily activities and quality of life.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria:Adults aged 18 years or older. 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. \- Exclusion Criteria: Participation in other structured physical exercise or rehabilitation programs during the study period. Presence of severe cardiovascular disease or uncontrolled medical conditions that contraindicate physical activity or electrostimulation. Neurological disorders or severe neuromuscular diseases. Use of anabolic drugs or medications that may interfere with muscle function. Pregnancy. Epilepsy. Active skin lesions or dermatological conditions in areas where electrodes are applied. Recent oncological surgery. 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. \-

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Conditions

The condition(s) this trial relates to.

long COVID-19 post-COVID-19 disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Long COVID Long COVID fatigue Post COVID syndrome Post COVID syndrome long COVID

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. A doctor treating you

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More trials for these conditions

Other studies related to the condition(s) this trial covers.