Accelerated TMS for Focal Hand Dystonia

Sponsor
Duke University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06015672
Collaborator
American Academy of Neurology (Other)
20
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Study Details

Study Description

Brief Summary

This study aims to investigate the impact of accelerated transcranial magnetic stimulation (TMS) on brain function and behavior in patients with focal hand dystonia. Previous research demonstrated that individualized TMS improved dystonic behavior after one session. Building on this, the current study administers four TMS sessions in a day, with assessments conducted on the same day, two weeks, and twelve weeks after each session. The research involves 10 in-person visits and focuses on functional MRI brain scans and writing behavior analysis. The potential risk of seizures from TMS is mitigated through careful screening, adhering to safety guidelines. The study's main benefit is enhancing dystonic behavior and deepening the understanding of brain changes caused by TMS in focal hand dystonia, paving the way for further advancements in clinical therapy for this condition.

Condition or Disease Intervention/Treatment Phase
  • Device: Transcranial Magnetic Stimulation (TMS)
N/A

Detailed Description

The primary aim of this research is to investigate the impact of transcranial magnetic stimulation (TMS) on both brain function and behavioral outcomes among individuals suffering from focal hand dystonia. A preliminary examination of a previous TMS study carried out by our team revealed that the application of TMS, using personalized, fMRI-guided brain targeting and interleaved TMS delivery during motor tasks, has the potential to modify brain activity and ameliorate dystonic behavior after a single session of TMS in patients with focal hand dystonia. This present study seeks to build upon these promising findings by administering four TMS sessions in a single day, interspersed with four rest intervals, a protocol referred to as "accelerated TMS." The investigation will consist of a total of ten in-person appointments. Participants with focal hand dystonia will receive accelerated TMS during three in-person visits. Following each TMS session, participants will evaluate changes in brain function and behavior. During the assessment visits, individuals will undergo functional MRI brain scans and engage in writing tasks on an electronic tablet. The principal risk associated with TMS is the possibility of inducing a seizure. However, this study will strictly adhere to safety guidelines, utilizing TMS levels that have not previously been linked to seizures in properly screened individuals. Notably, the dosages of TMS proposed for use in this study have not caused seizures in healthy volunteers. To further mitigate the risk of seizures, potential subjects will undergo medical screening for any known factors that could predispose them to seizures. The primary advantage of this study lies in its potential to enhance dystonic behavior in patients with focal hand dystonia, while also deepening our comprehension of the foundational changes in brain function before and after TMS intervention for focal hand dystonia. The discoveries stemming from this investigation will pave the way for future research endeavors aimed at advancing brain stimulation as a viable clinical therapy for focal hand dystonia.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Single-arm crossover study design with subjects receiving TMS at two different intensities and two cortical locationsSingle-arm crossover study design with subjects receiving TMS at two different intensities and two cortical locations
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
The TMS intensity and cortical location delivered at each TMS visit will be masked
Primary Purpose:
Treatment
Official Title:
Duke Accelerated Transcranial Magnetic Stimulation for Focal Hand Dystonia
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Mar 9, 2024
Anticipated Study Completion Date :
Mar 9, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: TMS to premotor cortex

Participants receive TMS at premotor cortex

Device: Transcranial Magnetic Stimulation (TMS)
Participants will experience three accelerated transcranial magnetic stimulation (TMS) sessions, with 12 week (three-months) gap between each session.

Active Comparator: TMS to primary somatosensory cortex

Participants received TMS sessions at primary somatosensory cortex

Device: Transcranial Magnetic Stimulation (TMS)
Participants will experience three accelerated transcranial magnetic stimulation (TMS) sessions, with 12 week (three-months) gap between each session.

Sham Comparator: TMS at low amplitude to primary somatosensory cortex

Participants receive TMS at a cortical target at smaller amplitude

Device: Transcranial Magnetic Stimulation (TMS)
Participants will experience three accelerated transcranial magnetic stimulation (TMS) sessions, with 12 week (three-months) gap between each session.

Outcome Measures

Primary Outcome Measures

  1. Change in behavioral writing measure [0 days, 2 weeks, and 12 weeks post-TMS]

    Using change in peak accelerations to assess writing behavior

  2. Change in brain connectivity in the motor network [0 days, 2 weeks and 12 weeks post-TMS]

    using functional magnetic resonance imaging of the brain

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18yrs and older

  • Diagnosed with isolated focal hand by Neurologist

  • Right-hand dominant

  • Must be able to sign an informed consent

  • Must be literate

Exclusion Criteria:
  • Other neurological movement disorders diagnoses including other types of dystonia, Parkinsonism, or essential tremor

  • History of seizure disorder

  • Concomitant medications are known to decrease seizure threshold

  • Illicit drug use

  • No TMS therapy for another indication within one month of this research study

  • Botulinum toxin injections within 3months of the research study

  • Medications used for symptom treatment of dystonia including anticholinergic, benzodiazepines, and muscle relaxants among others within one month of the study

  • No physical or occupational therapy of the hand within one month of the study

  • Any contraindications to MRI or TMS

Contacts and Locations

Locations

Site City State Country Postal Code
1 Duke University Health System Durham North Carolina United States 27705

Sponsors and Collaborators

  • Duke University
  • American Academy of Neurology

Investigators

  • Principal Investigator: Noreen Bukhari-Parlakturk, MD PhD, Duke Health

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT06015672
Other Study ID Numbers:
  • Pro00112239
First Posted:
Aug 29, 2023
Last Update Posted:
Aug 29, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 29, 2023