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Trial record 13 of 173 for:    Recruiting, Not yet recruiting, Available Studies | psychiatric disorder OR bipolar OR depression | Brain Stimulation

Non-invasive Brain Stimulation for the Treatment of Depression Symptoms in ALS

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ClinicalTrials.gov Identifier: NCT03373981
Recruitment Status : Recruiting
First Posted : December 14, 2017
Last Update Posted : February 1, 2019
Sponsor:
Information provided by (Responsible Party):
Hospital for Special Surgery, New York

Brief Summary:
This is an open-label clinical trial to determine the safety of rTMS and efficacy in improving depression symptoms, quality of life and cognition deficits among patients with Amyotrophic Lateral Sclerosis (ALS) and other neurodegenerative disorders.

Condition or disease Intervention/treatment Phase
ALS Device: rTMS Not Applicable

Detailed Description:

The objective of this study is to evaluate the role of repetitive transcranial magnetic stimulation (rTMS) for symptom reduction of depression and cognitive loss among patients with Amyotrophic Lateral Sclerosis (ALS) and other Neurodegenerative Diseases. Behavioral symptoms in ALS have been under scrutiny since its earliest descriptions, nearly 30 years ago (1). The importance of these symptoms among subjects with ALS has been also been under steady scrutiny. Studies have shown that the rates of anxiety and depression are significantly higher among subjects with ALS than the general population (1-23). Anxiety symptoms are related to depression, quality of life, and satisfaction with life (4, 9, 11, 15, 20, 24-26). Depressive symptoms are closely related to the ALS disease process (2).

rTMS has been shown to be a promising tool in modulating mood, memory, and cognitive performance (27). Current approaches to the management of ALS involve addressing symptomatology associated with the disease process. Among patients with ALS and other similar Neurodegenerative disorders, it is therefore important to understand if rTMS as an intervention is capable of:

  1. Symptomatic improvement in mood,
  2. Causing a significant positive change in disease progression or
  3. Helping improve quality of life.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 15 participants
Intervention Model: Single Group Assignment
Intervention Model Description: open label single arm
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Non-invasive Brain Stimulation for the Treatment of Depression Symptoms in ALS: A Pilot Study
Actual Study Start Date : November 29, 2017
Estimated Primary Completion Date : November 20, 2019
Estimated Study Completion Date : November 20, 2019

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: intervention
rTMS
Device: rTMS
repetitive transcranial magnetic stimulation




Primary Outcome Measures :
  1. To evaluate safety and efficacy of repetitive transcranial magnetic stimulation (rTMS) using the FDA approved protocol in research subjects with ALS and other Neurodegenerative disorders. [ Time Frame: over 4 weeks, done once a week ]
    Transcranial magnetic stimulation (TMS) is a non-invasive procedure used to stimulate small regions of the brain. It is a FDA approved for treatment resistant depression (K061053). We hypothesize that stimulation of dorsolateral prefrontal cortex (DLPFC) will be safe and effective in patients with ALS and other Neurodegenerative disorders. We will follow the FDA rTMS guidance for industry guidelines. All adverse events from all 15 patients enrolled in the study as assessed by the CTCAE v4.0, and as well, any occurrence of any new seizure in 2 or more patients, as reviewed and assessed by PI and medical monitor.


Secondary Outcome Measures :
  1. To understand the impact of rTMS in addressing the mood symptoms associated with ALS. [ Time Frame: recorded once a week for the 4 week duration of the study. ]
    rTMS is known to ameliorate depressive symptoms in patients with treatment resistant depression. It may also ameliorate depressive symptoms in subjects with ALS. This is measured using MQOL (Montreal Quality of life scale). This is a patient-reported instrument designed to assess overall well-being over a two day time scale. this single item scale is scored from 0-10 with higher score representing higher quality of life ratings. percent change from baseline to study completion will be measured to assess the efficacy of rtms in improving overall quality of life.



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Ages Eligible for Study:   18 Years to 99 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Diagnosis of familial or sporadic ALS as well as other Neurodegenerative disorders. Verification of the diagnosis will be performed by the Principal Investigator. This diagnosis can include neuro-degenerative disorders of uncertain cause, including ALS, MND, Peripheral neuropathies, Parkinson's and other progressive motor system diseases.
  2. If subjects has ALS diagnosis, the date of dx should be ≤ 2 years
  3. Age 18 or older.
  4. Capable of providing informed consent.
  5. Minimal speech impairment.
  6. Ability to comply with study procedures.
  7. Ability to communicate clearly if the subject wants to withdraw from the procedure at any stage.
  8. MMSE ≥20
  9. Female subjects of child bearing potential must engage in abstinence for the duration of the study. If a participant becomes sexually active, she must agree to using the following birth control methods:

    1. Hormonal (oral, implanted, injected, etc)
    2. Intrauterine device in place for ≥ 3 months
    3. Adequate barrier method in conjunction with spermicide
    4. Other
  10. Absence of exclusion criteria.

EExclusion Criteria

  1. Unable to provide informed consent
  2. Significant speech impairment
  3. Inability to comply with the procedures
  4. Subjects with ALS diagnosis ≥ 2 years
  5. Inability to communicate clearly if the subject wants to withdraw from the procedure at any stage
  6. Seizures or history of seizures
  7. Patients who have underwent brain surgery for any indication
  8. Patients with pacemakers, cochlear implants, brain stimulators, infusion pumps, intracardiac lines, metallic clips, other implanted electronic or ferroelectric metallic devices. Dental implants are permitted
  9. Inability to perform either TMS or NCS studies due to insufficient MEP or CMAP amplitude.
  10. Patients with uncontrolled hypertension
  11. Patients with neuro endocrine disorders
  12. Patients who are withdrawn from the following drugs within 6 months:

    • Barbiturates
    • Benzodiazepines
    • Meprobamate
    • Chloral hydrate

Patients who have a recent history (within 24h) or chronic history of intake of:

  • Cocaine.
  • Phencyclidine Phosphate.
  • Gamma-Hydroxy Butyrate.
  • Amphetamines including N-methylamphetamine, 3,4-Methylenedioxymethamphetamine, 2,5-dimethoxy-4-methylamphetamine, Ephedrine, Cathinone.

    12. Substance abuse+ 13. Excessive use of alcohol # 14. MMSE ≤19 15. Female patients of child bearing potential not practicing contraception 16. Female patients who are pregnant


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03373981


Contacts
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Contact: Mona Shahbazi 2127742361 shahbazim@hss.edu
Contact: Shara Holzberg holzbergs@hss.edu

Locations
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United States, New York
Hospital for Special Surgery Recruiting
New York, New York, United States, 10021
Contact: Mona Shahbazi       shahbazim@hss.edu   
Sponsors and Collaborators
Hospital for Special Surgery, New York

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Responsible Party: Hospital for Special Surgery, New York
ClinicalTrials.gov Identifier: NCT03373981     History of Changes
Other Study ID Numbers: 2016-0326
First Posted: December 14, 2017    Key Record Dates
Last Update Posted: February 1, 2019
Last Verified: January 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: No
Pediatric Postmarket Surveillance of a Device Product: No
Product Manufactured in and Exported from the U.S.: Yes
Additional relevant MeSH terms:
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Depression
Behavioral Symptoms