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Theta Burst Transcranial Magnetic Stimulation as Treatment for Auditory Verbal Hallucinations

Primary Purpose

Schizophrenia, Psychotic Disorders

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Theta Burst Transcranial Magnetic Stimulation
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Auditory verbal hallucinations, Transcranial Magnetic stimulation, Theta Burst frequency

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of schizophrenia, schizophreniform disorder, schizoaffective disorder or psychosis not otherwise specified.
  • Age 18+ years.
  • Frequent auditory verbal hallucinations (cut-off at >once an hour).
  • Written informed consent.

Exclusion Criteria:

  • Metal objects in or around the head that cannot be removed (i.e. cochlear implant, surgical clips, piercing, cardiac pacemaker, medicinal pumps)
  • History of seizures
  • Increased intracranial pressure due to infarcts or trauma.
  • History of eye trauma with a metal object or professional metal workers
  • Patients who are coercively treated at a psychiatric ward (based on a judicial ruling)
  • Patients who are represented by a legal ward or under legal custody
  • In female patients, there should be no possibility for pregnancy as determined with a pregnancy test
  • Changes in the prescribed medication in a period of 2 weeks prior to participation

Sites / Locations

  • UMC Utrecht

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Theta burst treatment

sham treatment

Arm Description

patients randomized to this arm will receive 10 TBS treatments distributed over 5 days

Outcomes

Primary Outcome Measures

Change in severity and frequency of auditory verbal hallucinations
This is as experienced by the participant. The change in score on the Auditory Hallucination Assessment Scale (AHAS; Frederick, 2000), the PSYRATS (Haddock et al., 1999) and the total score on the PANSS item 3 (Kay et al. 1987), the item concerning the severity of the hallucinations, after one week of treatment end one month after treatment will be used for this outcome.

Secondary Outcome Measures

Number and severity of adverse events
This is measured by the use of a selection of the Global index of Safety (Prieto, Sacristan & Gomez, 2004). The scores on this questionnaire are compared between the two conditions.

Full Information

First Posted
January 9, 2012
Last Updated
September 24, 2014
Sponsor
UMC Utrecht
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1. Study Identification

Unique Protocol Identification Number
NCT01512290
Brief Title
Theta Burst Transcranial Magnetic Stimulation as Treatment for Auditory Verbal Hallucinations
Official Title
Theta Burst Transcranial Magnetic Stimulation as Treatment for Auditory Verbal Hallucinations; a Placebo-controlled Trail
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Auditory verbal hallucinations (AVH) are a characterising symptom of schizophrenia. In the majority of patients, these AVH respond well to antipsychotic medication. Yet, a significant minority continues to experience frequent AVH despite optimal pharmacotherapy. The number of alternative treatment options for this medication resistant group is currently low and most of them focus on coping with the hallucinations. Transcranial magnetic stimulation (TMS), in contrast, is a non-invasive technique of influencing cortical excitability. This technique has the potential to actually decrease the frequency and severity of medication resistant hallucinations. Several previous studies have assessed efficacy of low frequency rTMS, with contradicting results. A previous large study by the investigators group could not demonstrate efficacy of low frequency rTMS. A new stimulation protocol using theta burst rTMS (TBS) could provide a more effective therapeutic option. Objective: The present study aims to examine the efficacy of TBS on the severity of AVH. Study design: The objectives are tested in a randomized double blind placebo-controlled trail. Study population: 60 patients with the diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder or psychosis not otherwise specified with frequent auditory verbal hallucinations will be included. Intervention: The participant will receive either 10 TBS treatments or 10 placebo treatments consisting of 900 pulses each with a 30 minute interval on the left temporoparietal area, distributed over 5 treatment days. Stimulation will be at 80% of the motor threshold. Main study parameters/endpoints: the main study parameter is the change in the severity of the AVH. The secondary study parameter is the number and severity of adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Psychotic Disorders
Keywords
Auditory verbal hallucinations, Transcranial Magnetic stimulation, Theta Burst frequency

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
71 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Theta burst treatment
Arm Type
Active Comparator
Arm Description
patients randomized to this arm will receive 10 TBS treatments distributed over 5 days
Arm Title
sham treatment
Arm Type
Placebo Comparator
Intervention Type
Other
Intervention Name(s)
Theta Burst Transcranial Magnetic Stimulation
Intervention Description
This rTMS paradigm consists of 5 pulses at 50Hz repeated at 5Hz for 60 seconds with a total of 900 pulses per treatment
Primary Outcome Measure Information:
Title
Change in severity and frequency of auditory verbal hallucinations
Description
This is as experienced by the participant. The change in score on the Auditory Hallucination Assessment Scale (AHAS; Frederick, 2000), the PSYRATS (Haddock et al., 1999) and the total score on the PANSS item 3 (Kay et al. 1987), the item concerning the severity of the hallucinations, after one week of treatment end one month after treatment will be used for this outcome.
Time Frame
1 week/ 1 month
Secondary Outcome Measure Information:
Title
Number and severity of adverse events
Description
This is measured by the use of a selection of the Global index of Safety (Prieto, Sacristan & Gomez, 2004). The scores on this questionnaire are compared between the two conditions.
Time Frame
1 week/ 1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of schizophrenia, schizophreniform disorder, schizoaffective disorder or psychosis not otherwise specified. Age 18+ years. Frequent auditory verbal hallucinations (cut-off at >once an hour). Written informed consent. Exclusion Criteria: Metal objects in or around the head that cannot be removed (i.e. cochlear implant, surgical clips, piercing, cardiac pacemaker, medicinal pumps) History of seizures Increased intracranial pressure due to infarcts or trauma. History of eye trauma with a metal object or professional metal workers Patients who are coercively treated at a psychiatric ward (based on a judicial ruling) Patients who are represented by a legal ward or under legal custody In female patients, there should be no possibility for pregnancy as determined with a pregnancy test Changes in the prescribed medication in a period of 2 weeks prior to participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iris Sommer, Prof., Dr.
Organizational Affiliation
UMC Utrecht
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anne Lotte Meijering, MSc.
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
Facility Information:
Facility Name
UMC Utrecht
City
Utrecht
ZIP/Postal Code
3584 CX
Country
Netherlands

12. IPD Sharing Statement

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Theta Burst Transcranial Magnetic Stimulation as Treatment for Auditory Verbal Hallucinations

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