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Recruiting NCT06696430

NCT06696430 Nudging to Promote the Use of Transcutaneous Electrical Nerve Stimulation for Postoperative Pain Relief

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Clinical Trial Summary
NCT ID NCT06696430
Status Recruiting
Phase
Sponsor Pether Jildenstal
Condition Acute Postoperative Pain in Urological Surgery
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2024-12-10
Primary Completion 2025-04-14

Trial Parameters

Condition Acute Postoperative Pain in Urological Surgery
Sponsor Pether Jildenstal
Study Type OBSERVATIONAL
Phase N/A
Enrollment 500
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-12-10
Completion 2025-04-14
Interventions
Educational Intervention on TENS UsageNudging Intervention to Promote TENS Usage

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Brief 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.

Eligibility Criteria

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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