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App-Based study aims to improve chronic pain tracking

NCT ID NCT05775510

Knowledge-focused Sponsor: MedtronicNeuro Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 looked at using a mobile app to collect feedback from 91 adults with chronic pain who were already receiving spinal cord stimulation (SCS) therapy. The goal was to see how well the app worked for gathering information on their pain and overall improvement. The study did not test a new treatment, but rather a new way to collect data.

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

91 people

The number who actually took part.

Started

Apr 2023

Finished

May 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

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 intended study population is adults with chronic, intractable pain of the trunk and/or limbs indicated to receive a Medtronic SCS system. Study eligibility criteria must be met to participate in this study.

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.

Pilot Phase Inclusion Criteria: 1. 18 years of age or older 2. A clinical decision was made for the patient to receive a commercial Medtronic SCS system (trial and implant) limited to the components for an on-label indication prior to enrollment in the study. NOTE: Vectris™ SureScan™ MRI 1x8 subcompact and Specify™SureScan™ MRI 2x8 leads are not eligible system components 3. Able to differentiate between pain associated with the indication for SCS implant and other types of pain, as determined by the Investigator or designee 4. Willing and able to use a personal smart phone for study surveys. NOTE: All subjects participating in the study must be willing to download the InsightPro™ clinical trial app and maintain current software updates on their own smart phone. 5. Willing and able to provide signed and dated informed consent in English 6. Willing and able to comply with all study procedures and visits Pilot Phase Exclusion Criteria: 1. Any active implantable neuromodulation device or system (e.g., Peripheral Nerve Stimulation, Sacral Neuromodulation) 2. Currently participating, or plans to participate, in another investigational study or has a planned major medical procedure that may interfere with study procedures or confound study results, as determined by the Investigator or designee, unless documented pre-approval is provided by the sponsor 3. Major untreated or refractory psychiatric comorbidity or other progressive disease (e.g., neurodegenerative disease, heart failure, cancer) that may confound study results, as determined by the Investigator or designee 4. Serious drug-related behavioral issues (e.g., alcohol dependency, illegal substance abuse), as determined by the Investigator or designee 5. Pregnant or planning on becoming pregnant 6. Involved in an injury claim under current litigation, beneficiary of an injury claim, or receiving worker's compensation 7. Patients with buried lead trials/implants will be excluded from this study

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Conditions

The condition(s) this trial relates to.

Chronic Pain chronic pain syndrome Pain, Intractable

As listed by the trial registrant

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

Pain, chronic Pain, intractable

Contacts and locations

Locations

  • Coastal Research Institute

    Carlsbad, California, 92009, United States

  • Garden State Pain and Orthopedics

    Clifton, New Jersey, 07013, United States

  • North Texas Orthopedics and Spine Center

    Grapevine, Texas, 76051, United States

  • Novant Health Spine Specialists

    Winston-Salem, North Carolina, 27103, United States

  • Oklahoma Pain Management

    Oklahoma City, Oklahoma, 73134, United States

  • Pain Diagnostics and Interventional Care

    Sewickley, Pennsylvania, 15143, United States

  • Pain Management Consultants of Southwest Florida

    Fort Myers, Florida, 33907, United States

  • Procura Pain and Spine PLLC

    Shenandoah, Texas, 77384, United States

  • The San Antonio Orthopaedic Group

    San Antonio, Texas, 78235, United States

  • Twin Cities Pain Clinic

    Edina, Minnesota, 55439, United States

More trials for these conditions

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