The Teaspoon Study: Telefitting Spinal Cord Stimulation for Pain

This study, called 'The Teaspoon Study,' is looking at different ways to use spinal cord stimulation (a device that sends mild electrical pulses to block pain signals) for people with chronic back pain or radiculopathy (nerve pain). Spinal cord stimulation can help improve pain, quality of life, and reduce disability. However, it sometimes doesn't work well in the long term. This study will have participants try out different types of stimulation (tonic, burst, and multistim) without knowing which type they are receiving. The main goal is to see if this approach is practical and can be done successfully over three years. You might be able to join if you are 22 or older, speak English, have a pain rating of 6 or higher, and are already scheduled for spinal cord stimulation. This study is currently recruiting 15 participants.

Study design
This is an interventional study involving 15 participants. Participants will try different types of stimulation but will not know which type they are receiving (blinded).
What's involved
Participants will undergo a structured process to evaluate different types of spinal cord stimulation.
Compensation
Not stated in the trial record.
Follow-up
The study will assess feasibility at 3 years.

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NCT05741788

The Teaspoon Study - Telefitting Spinal Cord Stimulation for Pain

Recruiting
NAAges 22+InterventionalTreatment
University of Minnesota
~15 participants
Updated 2025-10-02 on ClinicalTrials.gov
What's tested:Various Stimulation Patterns

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility
Measured over 3 years
Spinal Cord Injuries
Chronic Pain
1 sites across 1 states
Minnesota1
  • David Darrow, MD · PRINCIPAL_INVESTIGATOR · University of Minnesota

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

22 years of age or older
Scheduled to undergo spinal cord stimulation
English speaker
Baseline pain rating (NRS/VAS) \>=6

Exclusion

Scheduled for permanent implantation only without trial
Presence of pacemakers or other neurostimulators
Pregnant
Inability to read or use smart phone
Individuals who are unable to consent
Employees or students of PI
Prisoners
  • Feasibility3 years

    Feasibility as measured by total study procedure completion rate.