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Evaluating the Efficacy and Safety of Octane Aether for Treating Chronic Low Back Pain

27. Mai 2026 aktualisiert von: Octane Innovation Inc.

A Randomized, Double-blind, Sham-controlled Study to Evaluate the Efficacy and Safety of the Octane [Aether] Bioelectricity Device for the Management of Chronic Low Back Pain

The goal of this clinical trial is to evaluate the safety of the Octane Aether device and to determine whether the device is effective in treating symptoms of non-specific chronic low back pain in adults. The Octane Aether is a wearable device that produces specific magnetic field outputs and is designed for daily use in a home setting. The main objectives of the trial are:

  • To measure the change in patient-reported pain scores during active treatment with the device compared to a sham treatment, and
  • To define and describe the adverse effects, if any, of the Octane Aether device when administered according to the protocol.

Every participant will evaluate three active output modes and a sham output using the same device. Patient-reported outcomes will inform the effectiveness of each output mode and help identify the need for personalization in magnetic field therapy.

Participants will:

  • Use the device at home for 60 minutes every day for 10 weeks,
  • Report daily pain scores using an electronic visual analog scale for pain intensity,
  • Visit the clinic 5 times over the course of the 13 week trial for checkups and device changes,
  • Respond to 3 phone calls for checkups, and
  • Fill various questionnaires related to disability, quality of life, and their back pain.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

24

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Kanada
    • Ontario
      • Kingston, Ontario, Kanada, K7K 0J7
        • Kingston Orthopaedic Pain Institute
        • Kontakt:
        • Hauptermittler:
          • Thomas Gregory

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • Able to provide informed consent;
  • Aged 18-65;
  • Pain intensity of at least 5 on a numerical rating scale (0-10);
  • Experiencing chronic low back pain that has persisted for ≥3 months;
  • Pain localized primarily to the lumbar spine region;
  • Conservative treatments, such as physical therapy, NSAIDs and lifestyle changes, have failed over the past 6 months. Participants are allowed to continue conservative treatments, but changes to use/frequency will be tracked; and
  • Must be able to attend 5 in-person clinic appointments over the 13-week study period.

Exclusion Criteria:

  • Began using new prescription medication for pain within the past 3 months;
  • Lumbar spine surgery (within the past 12 months);
  • Body Mass Index (BMI)> 35. The device may have diminished effectiveness and/or may not fit individuals with high BMI;
  • Presence of a cardiac pacemaker;
  • Pregnancy or breastfeeding;
  • Presence of ferromagnetic implants or body piercings (e.g., navel piercings) in the lumbar region, including hip implants/replacements or similar in the pelvic region, that could interfere with device function;
  • Inability to put on, adjust, and/or operate the wearable device without assistance;
  • Prior use of PEMF, or other electromagnetic field-emitting device, for the treatment of pain symptoms;
  • No, or inconsistent, access to internet (emailed surveys are used for daily data collection); and
  • Any condition or diagnosis that could in the opinion of the Principal Investigator or delegate interfere with the participant's ability to comply with study instructions, might confound the interpretation of the study results, or put the participant at risk.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Crossover-Aufgabe
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Sequence Group 1
Participants receive active/sham treatments in the following sequence: EMF A, EMF B, Sham, EMF C
Gerät: Pulsed electromagnetic field stimulator

The Octane Aether is a body-worn device that generates pulsed magnetic fields of specific characteristics designed to target cellular behaviour in relation to chronic pain signalling. The device features four different output modes (3 active and 1 sham) to enable an investigation of the need for personalized pain management. The specific characteristics of the output modes are blinded from the participants and study team and are labelled here as EMF A, EMF B, EMF C, and Sham. The device firmware is programmed to automatically change the output mode every two weeks. The device produces no sound or thermal effects.

When operating in the sham mode, the device appears identical to active output, but no current is applied to the body-worn coil applicator and no magnetic field is generated.

Andere Namen:
  • Octane Aether
  • Octane Bioelectricity Device
  • PEMF device
  • EMF therapy
Experimental: Sequence Group 2
Participants receive active/sham treatments in the following sequence: EMF B, EMF C, EMF A, Sham
Gerät: Pulsed electromagnetic field stimulator

The Octane Aether is a body-worn device that generates pulsed magnetic fields of specific characteristics designed to target cellular behaviour in relation to chronic pain signalling. The device features four different output modes (3 active and 1 sham) to enable an investigation of the need for personalized pain management. The specific characteristics of the output modes are blinded from the participants and study team and are labelled here as EMF A, EMF B, EMF C, and Sham. The device firmware is programmed to automatically change the output mode every two weeks. The device produces no sound or thermal effects.

When operating in the sham mode, the device appears identical to active output, but no current is applied to the body-worn coil applicator and no magnetic field is generated.

Andere Namen:
  • Octane Aether
  • Octane Bioelectricity Device
  • PEMF device
  • EMF therapy
Experimental: Sequence Group 3
Participants receive active/sham treatments in the following sequence: EMF C, Sham, EMF B, EMF A
Gerät: Pulsed electromagnetic field stimulator

The Octane Aether is a body-worn device that generates pulsed magnetic fields of specific characteristics designed to target cellular behaviour in relation to chronic pain signalling. The device features four different output modes (3 active and 1 sham) to enable an investigation of the need for personalized pain management. The specific characteristics of the output modes are blinded from the participants and study team and are labelled here as EMF A, EMF B, EMF C, and Sham. The device firmware is programmed to automatically change the output mode every two weeks. The device produces no sound or thermal effects.

When operating in the sham mode, the device appears identical to active output, but no current is applied to the body-worn coil applicator and no magnetic field is generated.

Andere Namen:
  • Octane Aether
  • Octane Bioelectricity Device
  • PEMF device
  • EMF therapy
Experimental: Sequence Group 4
Participants receive active/sham treatments in the following sequence: Sham, EMF A, EMF C, EMF B
Gerät: Pulsed electromagnetic field stimulator

The Octane Aether is a body-worn device that generates pulsed magnetic fields of specific characteristics designed to target cellular behaviour in relation to chronic pain signalling. The device features four different output modes (3 active and 1 sham) to enable an investigation of the need for personalized pain management. The specific characteristics of the output modes are blinded from the participants and study team and are labelled here as EMF A, EMF B, EMF C, and Sham. The device firmware is programmed to automatically change the output mode every two weeks. The device produces no sound or thermal effects.

When operating in the sham mode, the device appears identical to active output, but no current is applied to the body-worn coil applicator and no magnetic field is generated.

Andere Namen:
  • Octane Aether
  • Octane Bioelectricity Device
  • PEMF device
  • EMF therapy

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in patient-reported pain scores during active treatment compared to the sham treatment period
Zeitfenster: From start of Treatment Period 1 (Week 2) to end of Treatment Period 4 (Week 9)
The difference in the mean pain VAS of scores reported in the second week of each active treatment period and the mean VAS of the second week of the same participant's sham period.
From start of Treatment Period 1 (Week 2) to end of Treatment Period 4 (Week 9)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Adverse effects associated with the use of the Octane Aether
Zeitfenster: From start of device use (Week 2) to follow-up appointment (Week 13 - end of study)
To define and describe the adverse effects of the Octane Aether when administered according to the clinical trial protocol. Participants and the study team will report adverse events associated with use of the device or device malfunctions.
From start of device use (Week 2) to follow-up appointment (Week 13 - end of study)
Effect of treatment on quality of life and disability index
Zeitfenster: From end of first treatment period (Week 3) to end of fourth treatment period (Week 9)
The Octane Aether's effect is evaluated using the Roland-Morris Disability questionnaire, which assesses low back pain's influence on disability and quality of life. The questionnaire is completed after each active and sham treatment period and compared.
From end of first treatment period (Week 3) to end of fourth treatment period (Week 9)
Net change in perceived pain intensity (start to end)
Zeitfenster: From baseline week (pre-intervention) to end of Treatment Period 4 (Week 9)
The change in mean pain VAS scores from the baseline week to the final week of Treatment Period 4 (Week 9).
From baseline week (pre-intervention) to end of Treatment Period 4 (Week 9)
Net effect of intervention on disability index
Zeitfenster: From baseline (Week 1) to end of Treatment Period 4 (Week 9)
Change in Roland-Morris Disability questionnaire responses from Baseline to end of Treatment Period 4.
From baseline (Week 1) to end of Treatment Period 4 (Week 9)
Effect of Octane Aether EMF treatment on general health (physical and emotional)
Zeitfenster: From Week 1 to Week 9
Participants respond to the RAND 36-item health survey after Week 1 and Week 9 and the change in category scores associated with physical and emotional health and quality of life are analyzed.
From Week 1 to Week 9
Longevity of the effect of Octane Aether treatment
Zeitfenster: From end of device use (Week 11) to follow-up appointment (Week 13)
VAS for pain reports are used to assess changes in pain intensity two weeks after the end of intervention use to evaluate whether there is a lasting effect from the treatment.
From end of device use (Week 11) to follow-up appointment (Week 13)
Longevity of the intervention effect on disability and quality of life
Zeitfenster: From end of device use (Week 11) to follow-up appointment (Week 13)
Roland-Morris Disability Questionnaire responses are used to evaluate the potential lasting effect of the interventional device after stopping daily use.
From end of device use (Week 11) to follow-up appointment (Week 13)

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Effectiveness of EMF A vs B vs C
Zeitfenster: From Treatment Period 1 (Week 2) to 4 (Week 9)
Compare the change in pain VAS scores reported from start to finish of each active and sham output mode.
From Treatment Period 1 (Week 2) to 4 (Week 9)
Output mode preference
Zeitfenster: Treatment Period 5 (Week 10)
Tally of output mode that each participant chose to repeat during Treatment Period 5. Participants are asked to select their preferred mode.
Treatment Period 5 (Week 10)
Changes in medication use
Zeitfenster: Responses recorded at Baseline and all scheduled appointments (after Week 1, 3, 5, 7, 9, 11, and 13)
To assess whether the use of the interventional device affects how participants report using (non-prescription) medication (dosage and frequency).
Responses recorded at Baseline and all scheduled appointments (after Week 1, 3, 5, 7, 9, 11, and 13)
Device performance - Temperature
Zeitfenster: Measurement data exported from the device after the device is returned during the Week 11 appointment.
Device performance is assessed by analyzing coil temperature sensor measurements recorded whenever the device is in use. Temperature data is compared to calibration measurements.
Measurement data exported from the device after the device is returned during the Week 11 appointment.
Device performance - Magnetic Flux Density
Zeitfenster: Measurement data exported from the device after the device is returned during the Week 11 appointment.
Device performance is assessed by analyzing magnetic flux density measurements collected using a Hall-effect sensor embedded in the coil applicator. Magnetic flux density data recorded during each treatment session is compared to calibration measurements as a measure of performance and consistency.
Measurement data exported from the device after the device is returned during the Week 11 appointment.
Device performance - Current
Zeitfenster: Measurement data exported from the device after the device is returned during the Week 11 appointment.
Device performance is assessed by analyzing data received from a current sensor that measures the current through the coil applicator. Current measurements, recorded during each treatment session, are compared to calibration data at the end of the study.
Measurement data exported from the device after the device is returned during the Week 11 appointment.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Octane Innovation Inc.

Mitarbeiter

Kingston Health Sciences Centre
Limestone Clinical Trial Unit
Providence Care, Kingston, ON, Canada

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juni 2026

Primärer Abschluss (Geschätzt)

1. Juni 2027

Studienabschluss (Geschätzt)

1. Juli 2027

Studienanmeldedaten

Zuerst eingereicht

14. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

27. Mai 2026

Zuerst gepostet (Tatsächlich)

29. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

27. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • Bioelectricity_FP01

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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