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Repetitive Transcranial Magnetic Stimulation as Therapy for Depression in Amyotrophic Lateral Sclerosis

Primary Purpose

Amyotrophic Lateral Sclerosis

Status
Withdrawn
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
active repetitive transcranial magnetic stimulation
sham repetitive transcranial magnetic stimulation
Sponsored by
Jagiellonian University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amyotrophic Lateral Sclerosis focused on measuring Amyotrophic Lateral Sclerosis, depression, rTMS

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of definite or probable ALS according to el Escorial criteria (Brooks et al. 2000)
  • Depression defined as the score in Beck's Depression Inventory ≥14
  • Mini-Mental State Examination score ≥26

Exclusion Criteria:

  • Psychiatric symptoms, which may negatively influence patient's tolerance and adherence to therapy
  • Respiratory insufficiency and other complications od advanced stages of ALS, which may compromise patient's ability to undergo the study procedure
  • Contraindications for rTMS as listed by the Guidelines of the International Federation of Clinical Neurophysiology (Rossi et al. 2009) i.e. seizure in the past, epilepsy, presence of magnetic material in the reach of magnetic field, pregnancy, likelihood to get pregnant, intracranial electrodes, cardiac pacemaker or intracardiac lines, frequent syncopes

Sites / Locations

  • Jagiellonian University Medical College, Department of Neurology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

active repetitive transcranial magnetic stimulation

sham repetitive transcranial magnetic stimulation

Arm Description

10 hertz (Hz) rTMS will be administered over the left dorsolateral prefrontal cortex. Therapy will include 10 daily sessions (on consecutive week days). In every sessions 3000 magnetic pulses of 120% of the resting motor threshold intensity will be elicited.

Sham stimulation will mimic the active one except that the stimulating coil will be held perpendicularly to the scalp, which assures similar impression as the active stimulation but prevents that significant magnetic field will reach brain tissue.

Outcomes

Primary Outcome Measures

Beck's Depression Inventory ater rTMS, total score, range 0 to 63, with higher values representing a worse outcome
Change from baseline score in the Beck's Depression Inventory to the measurement taken directly after finishing rTMS.
Beck's Depression Inventory first follow up, total score, range 0 to 63, with higher values representing a worse outcome
Change from baseline score in the Beck's Depression Inventory to the measurement taken two weeks after finishing rTMS.
Beck's Depression Inventory second follow up, total score, range 0 to 63, with higher values representing a worse outcome
Change from baseline score in the Beck's Depression Inventory to the measurement taken four weeks after finishing rTMS.

Secondary Outcome Measures

Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised after rTMS, total score, range 0 to 40 with higher values representing a better outcome
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken directly after finishing rTMS.
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised first follow up, total score, range 0 to 40 with higher values representing a better outcome
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken two weeks after finishing rTMS.
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised second follow up, total score, range 0 to 40 with higher values representing a better outcome
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken directly after finishing rTMS.
Apathy Evaluation Scale Clinical Version ater rTMS, total score, range 18 to 72 with higher values representing a worse outcome
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken taken directly after finishing rTMS.
Apathy Evaluation Scale Clinical Version first follow up, total score, range 18 to 72 with higher values representing a worse outcome
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken two weeks after finishing rTMS.
AES-C second follow up, total score, range 18 to 72 with higher values representing a worse outcome
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken four weeks after finishing rTMS.

Full Information

First Posted
March 26, 2019
Last Updated
February 6, 2020
Sponsor
Jagiellonian University
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1. Study Identification

Unique Protocol Identification Number
NCT03892863
Brief Title
Repetitive Transcranial Magnetic Stimulation as Therapy for Depression in Amyotrophic Lateral Sclerosis
Official Title
A Pilot Study of Repetitive Transcranial Magnetic Stimulation for Improvement of Depression in Amyotrophic Lateral Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Withdrawn
Why Stopped
Participants were not able to stay for two weeks near our center.
Study Start Date
November 15, 2019 (Anticipated)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jagiellonian University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive loss of central and peripheral motor neurons. ALS leads to death usually within 3 to 5 years from the onset of the symptoms. Available treatment can prolong the disease duration but cannot modify the disease course. Depression is a frequent complication of ALS, which further decreases quality of life and the available data concerning effectivity of antidepressant drugs are conflicting. Repetitive Transcranial Magnetic Stimulation (rTMS) is a noninvasive method of modulation of brain plasticity with confirmed antidepressive effect. The purpose of this study is to compare the effectiveness of rTMS in improving the depression in patients with ALS with placebo stimulation. Intervention will include 10 daily sessions. In each session 3000 magnetic pulses will be administered over the left dorsolateral prefrontal cortex. Assessment depression severity will be made before and after therapy, as well as two and four weeks later.
Detailed Description
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive loss of central and peripheral motor neurons. ALS leads to death usually within 3 to 5 years from the onset of the symptoms. Available treatment can prolong the disease duration but cannot modify the disease course. Depression is a frequent complication of ALS, which further decreases quality of life and the available data concerning effectivity of antidepressant drugs are conflicting. Similarly, the apathy may also complicate ALS and worsen the prognosis. Repetitive Transcranial Magnetic Stimulation (rTMS) is a noninvasive method of modulation of brain plasticity with proved antidepressive effect in patients suffering from major depression and in depression associated with several neurological disorders such as Parkinson's disease or stroke. The purpose of this study is to compare the effectiveness rTMS in improving the depression and - as a secondary outcome - the apathy and daily functioning in patients with ALS. Intervention will include ten daily sessions of rTMS. In each session 3000 magnetic pulses will be administered over the left dorsolateral prefrontal cortex. Stimulation intensity will equal 120% of the motor threshold value for the right first dorsal interosseus. Assessment of depression severity and of apathy and daily functioning will be made before and after therapy, as well as two and four weeks later.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amyotrophic Lateral Sclerosis
Keywords
Amyotrophic Lateral Sclerosis, depression, rTMS

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomly assigned to real or placebo (sham) stimulation.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Sham stimulation will be provided by holding the stimulating coil perpendicularly to the scalp, which assures similar impression as during active stimulation but prevents significant magnetic field to reach the brain tissue.
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
active repetitive transcranial magnetic stimulation
Arm Type
Active Comparator
Arm Description
10 hertz (Hz) rTMS will be administered over the left dorsolateral prefrontal cortex. Therapy will include 10 daily sessions (on consecutive week days). In every sessions 3000 magnetic pulses of 120% of the resting motor threshold intensity will be elicited.
Arm Title
sham repetitive transcranial magnetic stimulation
Arm Type
Sham Comparator
Arm Description
Sham stimulation will mimic the active one except that the stimulating coil will be held perpendicularly to the scalp, which assures similar impression as the active stimulation but prevents that significant magnetic field will reach brain tissue.
Intervention Type
Device
Intervention Name(s)
active repetitive transcranial magnetic stimulation
Intervention Description
High frequency rTMS to induce the long term potentiation in the left dorsolateral prefrontal cortex
Intervention Type
Device
Intervention Name(s)
sham repetitive transcranial magnetic stimulation
Intervention Description
High frequency rTMS to induce the long term potentiation in the left dorsolateral prefrontal cortex
Primary Outcome Measure Information:
Title
Beck's Depression Inventory ater rTMS, total score, range 0 to 63, with higher values representing a worse outcome
Description
Change from baseline score in the Beck's Depression Inventory to the measurement taken directly after finishing rTMS.
Time Frame
Before rTMS, directly (on the same day) after finishing rTMS
Title
Beck's Depression Inventory first follow up, total score, range 0 to 63, with higher values representing a worse outcome
Description
Change from baseline score in the Beck's Depression Inventory to the measurement taken two weeks after finishing rTMS.
Time Frame
Before rTMS, two weeks after finishing rTMS
Title
Beck's Depression Inventory second follow up, total score, range 0 to 63, with higher values representing a worse outcome
Description
Change from baseline score in the Beck's Depression Inventory to the measurement taken four weeks after finishing rTMS.
Time Frame
Before rTMS, four weeks after finishing rTMS
Secondary Outcome Measure Information:
Title
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised after rTMS, total score, range 0 to 40 with higher values representing a better outcome
Description
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken directly after finishing rTMS.
Time Frame
Before rTMS, directly (on the same day) after finishing rTMS
Title
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised first follow up, total score, range 0 to 40 with higher values representing a better outcome
Description
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken two weeks after finishing rTMS.
Time Frame
Before rTMS, two weeks after finishing rTMS
Title
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised second follow up, total score, range 0 to 40 with higher values representing a better outcome
Description
Change from baseline score in the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised to the measurement taken directly after finishing rTMS.
Time Frame
Before rTMS, four weeks after finishing rTMS
Title
Apathy Evaluation Scale Clinical Version ater rTMS, total score, range 18 to 72 with higher values representing a worse outcome
Description
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken taken directly after finishing rTMS.
Time Frame
Before rTMS, directly (on the same day) after finishing rTMS
Title
Apathy Evaluation Scale Clinical Version first follow up, total score, range 18 to 72 with higher values representing a worse outcome
Description
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken two weeks after finishing rTMS.
Time Frame
Before rTMS, two weeks after finishing rTMS
Title
AES-C second follow up, total score, range 18 to 72 with higher values representing a worse outcome
Description
Change from baseline score in the Apathy Evaluation Scale Clinical Version to the measurement taken four weeks after finishing rTMS.
Time Frame
Before rTMS, four weeks after finishing rTMS

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of definite or probable ALS according to el Escorial criteria (Brooks et al. 2000) Depression defined as the score in Beck's Depression Inventory ≥14 Mini-Mental State Examination score ≥26 Exclusion Criteria: Psychiatric symptoms, which may negatively influence patient's tolerance and adherence to therapy Respiratory insufficiency and other complications od advanced stages of ALS, which may compromise patient's ability to undergo the study procedure Contraindications for rTMS as listed by the Guidelines of the International Federation of Clinical Neurophysiology (Rossi et al. 2009) i.e. seizure in the past, epilepsy, presence of magnetic material in the reach of magnetic field, pregnancy, likelihood to get pregnant, intracranial electrodes, cardiac pacemaker or intracardiac lines, frequent syncopes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jakub M Antczak, MD
Organizational Affiliation
Department of Neurology, Jagiellonian University Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jagiellonian University Medical College, Department of Neurology
City
Kraków
ZIP/Postal Code
31503
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After completing the study, the details of neurophysiologic diagnostics including motor threshold, the age and gender as well as individual scores of Mini-Mental State Examination, Beck depression inventory, AES-C and Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised will be made available to other researchers on request.
IPD Sharing Time Frame
The data will become available after the study is published.
IPD Sharing Access Criteria
On request send by e-mail: jantczak@cm-uj.krakow.pl
Citations:
PubMed Identifier
11464847
Citation
Brooks BR, Miller RG, Swash M, Munsat TL; World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Dec;1(5):293-9. doi: 10.1080/146608200300079536. No abstract available.
Results Reference
background
PubMed Identifier
15258224
Citation
Fregni F, Santos CM, Myczkowski ML, Rigolino R, Gallucci-Neto J, Barbosa ER, Valente KD, Pascual-Leone A, Marcolin MA. Repetitive transcranial magnetic stimulation is as effective as fluoxetine in the treatment of depression in patients with Parkinson's disease. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1171-4. doi: 10.1136/jnnp.2003.027060.
Results Reference
background
PubMed Identifier
25034472
Citation
Lefaucheur JP, Andre-Obadia N, Antal A, Ayache SS, Baeken C, Benninger DH, Cantello RM, Cincotta M, de Carvalho M, De Ridder D, Devanne H, Di Lazzaro V, Filipovic SR, Hummel FC, Jaaskelainen SK, Kimiskidis VK, Koch G, Langguth B, Nyffeler T, Oliviero A, Padberg F, Poulet E, Rossi S, Rossini PM, Rothwell JC, Schonfeldt-Lecuona C, Siebner HR, Slotema CW, Stagg CJ, Valls-Sole J, Ziemann U, Paulus W, Garcia-Larrea L. Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS). Clin Neurophysiol. 2014 Nov;125(11):2150-2206. doi: 10.1016/j.clinph.2014.05.021. Epub 2014 Jun 5.
Results Reference
background
PubMed Identifier
19833552
Citation
Rossi S, Hallett M, Rossini PM, Pascual-Leone A; Safety of TMS Consensus Group. Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin Neurophysiol. 2009 Dec;120(12):2008-2039. doi: 10.1016/j.clinph.2009.08.016. Epub 2009 Oct 14.
Results Reference
background
PubMed Identifier
28092847
Citation
Shen X, Liu M, Cheng Y, Jia C, Pan X, Gou Q, Liu X, Cao H, Zhang L. Repetitive transcranial magnetic stimulation for the treatment of post-stroke depression: A systematic review and meta-analysis of randomized controlled clinical trials. J Affect Disord. 2017 Mar 15;211:65-74. doi: 10.1016/j.jad.2016.12.058. Epub 2017 Jan 10.
Results Reference
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Repetitive Transcranial Magnetic Stimulation as Therapy for Depression in Amyotrophic Lateral Sclerosis

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