NCT03984201

Brief Summary

This study evaluates an accelerated schedule of theta-burst stimulation using a transcranial magnetic stimulation device for chronic pain. In this double blind, randomized control study, participants will be randomized to the treatment group to receive accelerated theta-burst stimulation or to a control group. All participants will be offered the open-label, active treatment 4 week prior to completing the initial 5 days of treatment.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Jun 2023

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 30, 2019

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 12, 2019

Completed
4 years until next milestone

Study Start

First participant enrolled

June 1, 2023

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2024

Completed
Last Updated

December 20, 2024

Status Verified

December 1, 2024

Enrollment Period

1.2 years

First QC Date

May 30, 2019

Last Update Submit

December 17, 2024

Conditions

Keywords

Chronic PainRepetitive Transcranial Magnetic Stimulation (rTMS)Accelerated Theta Burst Stimulation (aTBS)Stanford Accelerated Intelligent Neuromodulation Therapy (SAINT)

Outcome Measures

Primary Outcomes (2)

  • Change in the Brief Pain Inventory (BPI) score

    A self-report measure designed to enable investigators to easily obtain sensitive measures of the degree of depression and individual is experiencing. Scoring: 1. Pain Severity Score: This is calculated by adding the scores for questions 2, 3, 4 and 5 and then dividing by 4. This gives a severity score out of 10. 2. Pain Interference Score: This is calculated by adding the scores for questions 8a, b, c, d, e, f and g and then dividing by 7. This gives an interference score out of 10.

    Pre-treatment, immediately post-treatment

  • Change in the McGill Pain Questionnaire score

    A self-report questionnaire that allows individuals that assesses the quality and intensity of pain that is experienced. The pain rating index has 2 subscales: sensory subscale with 11 words, and affective subscale with 4 words. These items are rated on an intensity scale as 0 = none, 1 = mild, 2 = moderate and 3 = severe. There's also one item for present pain intensity and one item for a 10cm visual analogue scale for average pain.

    Pre-treatment, immediately post-treatment

Secondary Outcomes (4)

  • Change in the Montgomery Asberg Depression Rating Scale (MADRS) score

    Pre-treatment, immediately post-treatment, 2 weeks post-treatment, 4 weeks post-treatment

  • Change in teh Hamilton Rating Scale for Depression (HAM-17) score

    Pre-treatment, immediately post-treatment, 2 weeks post-treatment, 4 weeks post-treatment

  • Change in the Pain Catastrophizing Scale (PCS) score

    Pre-treatment, immediately post-treatment, 2 weeks post-treatment, 4 weeks post-treatment

  • Change in functional connectivity as measured by Functional Magnetic Resonance Imaging (fMRI)

    Pre-treatment, immediately post-treatment, 4 weeks post-treatment

Study Arms (3)

iTBS over L-DLPFC to dACC

ACTIVE COMPARATOR

Participants will receive iTBS (intermittent theta burst stimulation) to the left dorsal lateral prefrontal cortex (L-DLPFC) with high connectivity to the dorsal anterior cingulate cortex (dACC). The L-DLPFC will be targeted utilizing the Localite neuronavigation system. Stimulation intensity will be standardized at 90% of resting motor threshold adjust to the skull to cortical surface distance. Stimulation will be delivered to L-DLPFC using the MagPRo stimulator.

Device: Intermittent Theta Burst Stimulation (iTBS)

iTBS over L-DLPFC to sgACC

ACTIVE COMPARATOR

Participants will receive iTBS (intermittent theta burst stimulation) to the left dorsal lateral prefrontal cortex (L-DLPFC) with high connectivity to the subgenual cingulate cortex (sgACC). The L-DLPFC will be targeted utilizing the Localite neuronavigation system. Stimulation intensity will be standardized at 90% of resting motor threshold adjust to the skull to cortical surface distance. Stimulation will be delivered to L-DLPFC using the MagPRo stimulator.

Device: Intermittent Theta Burst Stimulation (iTBS)

Sham iTBS over L-DLPFC

SHAM COMPARATOR

Participants will receive sham iTBS (intermittent theta burst stimulation) to the left DLPFC. The L-DLPFC will be targeted utilizing the Localite neuronavigation system. Sham stimulation will be delivered to L-DLPFC using the MagPRo stimulator.

Device: Intermittent Theta Burst Stimulation (iTBS)

Interventions

Participants will receive active or sham transcranial magnetic stimulation delivered to the L-DLPFC.

Also known as: Accelerated Theta Burst Stimulation (aTBS), Repetitive Transcranial Magnetic Stimulation (rTMS)
Sham iTBS over L-DLPFCiTBS over L-DLPFC to dACCiTBS over L-DLPFC to sgACC

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients need to meet at least a 4/10 on a clinical pain rating scale and/or fulfill fibromyalgia diagnostic criteria on the 2010 Fibromyalgia Diagnostic Criteria (Wolfe et al., 2010)
  • Age 18 - 70
  • Right-handed
  • Agree to having fMRI scans as well as rTMS sessions
  • Proficiency in English sufficient to complete questionnaires / follow instructions during fMRI assessments and treatment
  • Women of childbearing potential must agree to use adequate contraception prior to study entry and continue this for the duration of the study
  • Participants may continue antidepressant regimen, but must be stable for 6 weeks prior to enrollment in the study. Antidepressant must be of the SSRI class only (if currently on a different antidepressant, patients will be switched to an SSRI). They must maintain that same antidepressant regimen throughout the study duration.

You may not qualify if:

  • History of MI, CABG, CHF, or other cardiac history.
  • Any condition that would contraindicate MRI (such as ferromagnetic metal in the body)
  • Pregnancy or breastfeeding
  • Any neurological condition, history of epilepsy, history of rTMS failure with FDA approved rTMS parameters, history of any implanted device or psychosurgery for depression, history of receiving ECT. OCD, narcolepsy or any additional significant neurological disorder as determined by the PI.
  • Autism spectrum disorder
  • Inability to stop taking medication contraindicated with treatment
  • Any significant psychiatric disorder as identified on the Mini International Neuropsychiatric Interview and determined by the PI
  • A positive urine toxicology screen

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Palo Alto, California, 94304, United States

Location

Related Publications (31)

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MeSH Terms

Conditions

Chronic Pain

Interventions

Transcranial Magnetic Stimulation

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Magnetic Field TherapyTherapeutics
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Blinded, randomized control
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Psychiatry and Behavioral Sciences

Study Record Dates

First Submitted

May 30, 2019

First Posted

June 12, 2019

Study Start

June 1, 2023

Primary Completion

August 1, 2024

Study Completion

August 1, 2024

Last Updated

December 20, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations