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Electric shocks may replace exercise for diabetes patients

NCT ID NCT02510521

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether using electrical stimulation on the thigh muscles could improve how the body uses insulin in people with type 2 diabetes. Eighteen adults with type 2 diabetes who were overweight and on oral medication received a single session and then six days of daily stimulation. The goal was to see if this method could serve as an alternative to physical activity for those unable to exercise.

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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

18 people

The number who actually took part.

Start date

Feb 2012

Finished

Jun 2014

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 75 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: * Men and women 18-75 years of age: * Type 2 diabetes, * in a context of overweight BMI upper than 25 kg / m², * a glycated hemoglobin included between 6 and 9%, * treated with oral antidiabetic (non glitazone) and / or GLP1 analogs (stable treatment for 3 months). * Patient who signed informed consent. Exclusion Criteria: * Type 1 diabetes * Children or adolescents under 18 years. * Patients over 75 years. * Pregnancy. * Patient intense practicing regular physical activity and do not wish to interrupt the time of the study * Patients with painful joint disease of the knee mobilization (osteoarthritis, inflammatory arthritis), any severe neuromuscular disease (diabetic neuropathy with pain, cramps, paresthesia, hypoesthesia, degenerative muscle disease). * Patients with unstable ischemic heart disease or arterial disease severe lower limbs. * Presence of a pacemaker (pacemaker). * Epilepsy * Patients insulin applicants * Treatment with glitazone. * Sepsis or other intercurrent acute disease (heart attack, angina ..). * Patients with skin lesions of any kind (wounds, inflammations, burns, irritations, eczema, etc.) nearby with areas for electrodes NMES * Patients unable to comply with the safety instructions of the NMES device at home * Patient unable to submit to medical monitoring study for geographical, social or psychological. * Patients under guardianship or trusteeship. * Patient included in another biomedical research protocol

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Endocrinology Unit and Clinical Research Center Basse Normandie, University Hospital of Caen

    Caen, 14000, France

More trials for these conditions

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