The Teaspoon Study - Telefitting Spinal Cord Stimulation for Pain
RecruitingNot applicableNCT05741788
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Spinal cord stimulation modulates the nervous system to effectively block pain signals originating from the back and legs. Spinal cord stimulation has been shown to improve chronic pain, improve quality of life, and reduce disability. Unfortunately, spinal cord stimulation has a high trial failure rate and a high long-term failure rate. This study consists of a prospective cohort of patients clinically scheduled to undergo spinal cord stimulation for the treatment of chronic back pain or radiculopathy. Participants will undergo a structured optimization evaluating existing types of stimulation (tonic, burst, and multistim). Each participant will try out all types of available stimulation but be blinded to the type. Over the course of four months, each participant will evaluate each type of stimulation by reporting daily pain scores. Thompson sampling will be used to identify which setting produces the biggest improvement in pain and recommend it for future use. Participants will follow up routinely to collect laboratory, behavioral, and survey responses to test for the feasibility of obtaining data explaining pain phenotype.
Study details
- Official title
- The Teaspoon Study - Telefitting Spinal Cord Stimulation for Pain
- Conditions
- Interventions
- Device: Various Stimulation Patterns
- Sponsor
- University of Minnesota
- Start date
- 2023-10-01
- Primary completion
- 2027-10-01
- Sex
- All
- Age range
- from 22 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 22 years of age or older * Scheduled to undergo spinal cord stimulation * English speaker * Baseline pain rating (NRS/VAS) \>=6 Exclusion Criteria: * 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
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05741788