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Treatment of Auditory Hallucinations in Schizophrenia With Bilateral Theta Burst Stimulation (cTBS-AH)

Primary Purpose

Auditory Hallucinations, Schizophrenia

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
MagPro Cool-B65A/P, Magventure
MagPro Cool-B65A/P, Magventure
Sponsored by
University Hospital Tuebingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Auditory Hallucinations focused on measuring auditory hallucinations, schizophrenia, cTBS, noninvasive brain stimulation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women, age 18-65 years
  • Schizophrenia (DSM-5 295.90), schizophreniform disorder (DSM-5, 295.40), or schizoaffective disorder (DSM-5 295.70)
  • Auditory hallucinations (AH) present at least once a week, for at least 3 months
  • No sufficient effect of at least one adequate antipsychotic treatment
  • Severity according to PANSS hallucination score (Item P3) of 3 or more
  • Fluent German language
  • Stable antipsychotic medication 2 weeks before and 3 weeks during the treatment

Exclusion Criteria:

  • Suicidality
  • History/evidence of brain surgery
  • Significant brain malformation or neoplasm
  • Head injury
  • Cerebral vascular events
  • Neurodegenerative disorder
  • Deep brain stimulation
  • Intracranial metallic particles
  • History of seizures
  • Diagnose of substance dependence or abuse as primary clinical problem
  • Severe somatic comorbidity
  • Cardiac pacemakers
  • Pregnancy

Sites / Locations

  • Department of Psychiatry and PsychotherapyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

active cTBS

Sham cTBS

Arm Description

Determination of resting motor threshold (RMT); Coil position: temporoparietal cortices halfway between T3/P3 and T4/P4 (EEG 10/20 system); active cTBS (80% of RMT);

Determination of resting motor threshold (RMT); Coil position: temporoparietal cortices halfway between T3/P3 and T4/P4 (EEG 10/20 system); sham cTBS;

Outcomes

Primary Outcome Measures

Change of Psychotic Symptom Rating Scales - Auditory Hallucinations subscale (PSYRATS-AH)
Group comparison (active vs. sham cTBS) regarding the change of the auditory hallucination subscale of the Psychotic Symptom Rating Scales (PSYRATS-AH) score from baseline to end of treatment period.

Secondary Outcome Measures

Full Information

First Posted
January 26, 2016
Last Updated
June 8, 2022
Sponsor
University Hospital Tuebingen
Collaborators
German Research Foundation, Institute for Clinical Epidemiology and Applied Biometry, University Tuebingen, Germany, Center for Clinical Studies, University Tuebingen (ZKS), Germany, Department of Psychiatry and Psychotherapy, University Munich (LMU), Germany, University of Ulm, Department of Psychiatry and Psychotherapy; University Heidelberg, Germany, Department of Psychiatry and Psychotherapy; Unversity Augsburg, Germany, Department of Psychiatry and Psychotherapy, LVR Duesseldorf, Germany
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1. Study Identification

Unique Protocol Identification Number
NCT02670291
Brief Title
Treatment of Auditory Hallucinations in Schizophrenia With Bilateral Theta Burst Stimulation
Acronym
cTBS-AH
Official Title
Treatment of Auditory Hallucinations in Schizophrenia With Bilateral Theta Burst Stimulation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 2017 (Actual)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Tuebingen
Collaborators
German Research Foundation, Institute for Clinical Epidemiology and Applied Biometry, University Tuebingen, Germany, Center for Clinical Studies, University Tuebingen (ZKS), Germany, Department of Psychiatry and Psychotherapy, University Munich (LMU), Germany, University of Ulm, Department of Psychiatry and Psychotherapy; University Heidelberg, Germany, Department of Psychiatry and Psychotherapy; Unversity Augsburg, Germany, Department of Psychiatry and Psychotherapy, LVR Duesseldorf, Germany

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized, sham-controlled, double blind, multicentre clinical trial aims at providing evidence for the efficacy and safety of continuous theta burst stimulation (cTBS) in the treatment of auditory hallucinations in patients with schizophrenia. Overall, the study will include 137 patients. Because of the adaptive study design, an interim analysis was performed after half of the originally planned patients (43/86), according to which the sample size was increased by 51 patients). Each patient will receive a three weeks course of daily (5/week) treatment; 50% of the patients will be treated with cTBS (1200 impulses daily), the other half with a sham stimulation to the left and right temporoparietal cortex. Sham stimulation will be applied by an active sham-coil that allows for a double-blind treatment. Follow-up assessments 1, 3 and 6 months after treatment will investigate the stability of treatment effects.
Detailed Description
Auditory verbal hallucinations (AH), a cardinal feature of schizophrenia, are often severely distressing and increase the risk for violence and suicide. Although antipsychotic medication mostly exerts rapid beneficial effects on this symptom particularly in first-episode patients who continue on taking their medication (Sommer et al. 2012), in up to 25%-30% of all patients, such hallucinations persist (Shergill et al. 1998). The often progressive course of the disease and insufficient treatment adherence due to unwanted side effects significantly limit the treatment response. In turn, this lack of treatment efficacy also contributes to low treatment adherence which is generally associated with an unfavorable course of schizophrenia and increased relapse and readmission rate. New and effective treatments are therefore essential to reduce the massive individual burden and psychosocial costs associated with schizophrenia. Nevertheless, in the last decades, the hopes for new pharmacological treatment options have been disappointed and the pharmaceutical industry has apparently withdrawn from the development of new compounds for this disorder. Accordingly, the development of non-pharmacological approaches based on an increasing body of patho-physiological knowledge is even more needed to pave new ways for the treatment of this frequently detrimental symptom of schizophrenia. The main objective of the present study is to provide high-level evidence for efficacy and safety of continuous theta burst stimulation (cTBS) in the treatment of auditory hallucination (AH) by this first full-size multicenter (3 centers) controlled clinical trial. This is a double blind (actually triple blind, i.e. patient, clinical investigator, and person who will administer cTBS), randomized, sham-controlled clinical trial to test the efficacy and safety of bilateral (successively applied) daily cTBS to the temporoparietal cortex on the severity of AH. The study will be conducted in a two-armed parallel design in which 50 % of the patients will be treated with the verum stimulation and the other half of patients will receive the placebo / sham stimulation. The cTBS protocol follows the method by Huang et al. (2005) and our pilot study (Plewnia et al. 2014a) to achieve a lasting reduction of cortical excitability. Accordingly, each stimulation train (40 s) of cTBS consists of 600 stimuli applied in bursts of 3 pulses at 50 Hz given every 200 ms (5 Hz). Stimulation intensity is standardized at 80% of the resting motor threshold (RMT) and applied successively to each hemisphere. For the first session, the order of right and left hemisphere will be determined by randomization and will alternate in each following session to preclude order effects.The RMT will be determined using EMG recordings from the left and right abductor pollicis brevis and defined as the minimal stimulation intensity needed to elicit at least 10 out of 20 motor-evoked-potentials of ≥ 50µV. RMT will be determined once, i.e. before the beginning of treatment period. The cTBS or sham treatment will be targeted both temporoparietal cortices halfway between T3/P3 and T4/P4 (EEG 10/20 system). The treatment (active cTBS or sham cTBS) will be administered over a period of 3 consecutive weeks at each workday (Monday to Friday), resulting in a total of 15 treatment sessions. Ratings will be performed after the last treatment of each week by an independent rater. Follow-up visits are planned 1, 3 and 6 months after end of treatment phase to control for sustainability of cTBS treatment effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Auditory Hallucinations, Schizophrenia
Keywords
auditory hallucinations, schizophrenia, cTBS, noninvasive brain stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
137 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
active cTBS
Arm Type
Active Comparator
Arm Description
Determination of resting motor threshold (RMT); Coil position: temporoparietal cortices halfway between T3/P3 and T4/P4 (EEG 10/20 system); active cTBS (80% of RMT);
Arm Title
Sham cTBS
Arm Type
Sham Comparator
Arm Description
Determination of resting motor threshold (RMT); Coil position: temporoparietal cortices halfway between T3/P3 and T4/P4 (EEG 10/20 system); sham cTBS;
Intervention Type
Device
Intervention Name(s)
MagPro Cool-B65A/P, Magventure
Intervention Description
combined active and sham coil
Intervention Type
Device
Intervention Name(s)
MagPro Cool-B65A/P, Magventure
Intervention Description
combined active and sham coil
Primary Outcome Measure Information:
Title
Change of Psychotic Symptom Rating Scales - Auditory Hallucinations subscale (PSYRATS-AH)
Description
Group comparison (active vs. sham cTBS) regarding the change of the auditory hallucination subscale of the Psychotic Symptom Rating Scales (PSYRATS-AH) score from baseline to end of treatment period.
Time Frame
3 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women, age 18-65 years Schizophrenia (DSM-5 295.90), schizophreniform disorder (DSM-5, 295.40), or schizoaffective disorder (DSM-5 295.70) Auditory hallucinations (AH) present at least once a week, for at least 3 months No sufficient effect of at least one adequate antipsychotic treatment Severity according to PANSS hallucination score (Item P3) of 3 or more Fluent German language Stable antipsychotic medication 2 weeks before and 3 weeks during the treatment Exclusion Criteria: Suicidality History/evidence of brain surgery Significant brain malformation or neoplasm Head injury Cerebral vascular events Neurodegenerative disorder Deep brain stimulation Intracranial metallic particles History of seizures Diagnose of substance dependence or abuse as primary clinical problem Severe somatic comorbidity Cardiac pacemakers Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christian Plewnia, Prof. MD.
Phone
+49 7071 29 86121
Email
christian.plewnia@uni-tuebingen.de
First Name & Middle Initial & Last Name or Official Title & Degree
Bettina Brendel, PhD.
Phone
+ 49 7071 29 87073
Email
bettina.brendel@uni-tuebingen.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Plewnia, Prof. MD.
Organizational Affiliation
Dept. Psychiatry and Psychotherapy, Universtiy of Tuebingen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychiatry and Psychotherapy
City
Tuebingen
ZIP/Postal Code
72076
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christian Plewnia, Prof. MD.
Phone
+49 7071 29 86121
Email
christian.plewnia@uni-tuebingen.de

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29224040
Citation
Plewnia C, Brendel B, Schwippel T, Martus P, Cordes J, Hasan A, Fallgatter AJ. Treatment of auditory hallucinations with bilateral theta burst stimulation (cTBS): protocol of a randomized, double-blind, placebo-controlled, multicenter trial. Eur Arch Psychiatry Clin Neurosci. 2018 Oct;268(7):663-673. doi: 10.1007/s00406-017-0861-3. Epub 2017 Dec 9.
Results Reference
derived

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Treatment of Auditory Hallucinations in Schizophrenia With Bilateral Theta Burst Stimulation

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