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Nudging (Influencing behavior and decisions) to promote the use of transcutaneous electrical nerve stimulation for postoperative pain relief

NCT ID NCT06696430

NEW Sponsor: Pether Jildenstal 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 09, 2026 · Last updated Sep 09, 2026

Summary

This study aims to increase the use of transcutaneous electrical nerve stimulation (TENS) for acute postoperative pain relief. TENS, a non-pharmacological treatment using electrical impulses, can enhance pain relief, reduce opioid use, and minimize side effects. Despite its benefits, TENS is underused in healthcare. This project will provide TENS education, support from experienced "superusers," and nudging techniques to encourage staff to adopt TENS, ultimately improving pain management and recovery for postoperative patients.

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.

Participants

500 people

The number who actually took part.

Started

Dec 2024

Finished

Sep 2026

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.

Who is studied

The study population includes healthcare staff working in the department where the study is conducted and patients who are scheduled for urological procedures under anesthesia and are 18 years or older. The focus is on observing and enhancing TENS usage in postoperative pain management within this specific clinical setting.

Ages

18 years and older

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: * All staff working in the department where the study will be conducted. * Patients scheduled for urological procedures under anesthesia who are 18 years of age or older. Exclusion Criteria: * Does not give consent. * Ongoing pregnancy. * Unable to speak or understand Swedish. * Presence of electronic implants (e.g., pacemaker, implantable - defibrillator/ICD). * Regular preoperative use of opioids. * Chronic pain condition. * Known substance abuse. * Reduced sensation at the site for TENS application. * Severe untreated psychiatric disorder.

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As listed by the trial registrant

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

Acute postoperative pain in urological surgery Pain management in postoperative care (including opioid-sparing approaches)

Contacts and locations

Locations

  • Sahlgrenska University Hospital

    Gothenburg, Sweden

  • Sahlgrenska university hospital

    Gothenburg, VGR, 43100, Sweden

  • Sahlgrenska university hospital

    Gotborg, Sweden

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