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Trial of Stimulus-response Potentiation in Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Auditory High Frequency Tetanizing Stimulation
Sham Comparator
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

20 Years - 50 Years (Adult)MaleAccepts Healthy Volunteers

For Schizophrenia group:

Inclusion Criteria:

  • Able to give written informed consent
  • Males (ages 20-50 years)
  • Diagnosis of schizophrenia as confirmed by Structured Clinical Interview for DSM-V-TR (SCID)
  • on stable doses of antipsychotic medications for at least 15 days
  • scores 4 or more on at least one item of the Positive and Negative Syndrome Scale.

Exclusion Criteria:

  • History of / or current medical/neurological illnesses e.g. mental retardation (DSM-V) or epilepsy or significant head trauma
  • Any type of hearing deficit will be excluded by audiometry assessment
  • Substance abuse in the past 2 months
  • medical conditions that make it difficult for the patient to visit the clinic in the designed schedule.

For control group:

Inclusion criteria:

  • able to give written informed consent
  • males (ages 20-50).

Exclusion criteria:

  • History of / or current medical/neurological illnesses e.g. mental retardation (DSM-V) or epilepsy or significant head trauma
  • Any type of hearing deficit
  • if they meet any axis-I diagnosis according to DSM-V confirmed by SCID.
  • scores 2 or more on one item of the Positive and Negative Syndrome Scale

Sites / Locations

  • Department of Psychiatry-Faculty of medicine-University of Cairo

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Sham Comparator

Experimental

Sham Comparator

Arm Label

Schizophrenia TS+ve

Schizophrenia TS-ve

Control TS+ve

Control TS-ve

Arm Description

Schizophrenia patients who receive auditory high frequency Tetanizing Stimulation

Schizophrenia patients who receive sham comparator

Healthy controls who receive auditory high frequency Tetanizing Stimulation

Healthy controls who receive sham comparator

Outcomes

Primary Outcome Measures

N100 wave (AEP) amplitude in µv [microvolts]
N100 or N1 is a large, negative-going evoked potential measured by electroencephalography. It peaks in adults between 80 and 120 milliseconds after the onset of a stimulus, and distributed mostly over the fronto-central region of the scalp.
P300 wave amplitude in µv [microvolts] (auditory odd-ball task)
The P300 (P3) wave is an event related potential (ERP) component elicited in the process of decision making. It is considered to be an endogenous potential, as its occurrence links not to the physical attributes of a stimulus, but to a person's reaction to it. More specifically, the P300 is thought to reflect processes involved in stimulus evaluation or categorization.

Secondary Outcome Measures

performance of Wisconsin Card Sorting test (WCST).
Wisconsin Card Sorting Test (WCST) is a neuropsychological test of "set-shifting", i.e. the ability to display flexibility in the face of changing schedules of reinforcement.

Full Information

First Posted
March 25, 2019
Last Updated
June 29, 2021
Sponsor
Cairo University
Collaborators
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT03892876
Brief Title
Trial of Stimulus-response Potentiation in Schizophrenia
Official Title
Pilot Trial of Stimulus-response Potentiation in Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
April 15, 2021 (Actual)
Study Completion Date
April 15, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
Collaborators
University of Pittsburgh

4. Oversight

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

5. Study Description

Brief Summary
This clinical trial aims at examining the effects of auditory high-frequency stimulation in schizophrenia patient, aiming to increase their AEPs, which are known to be attenuated from previous literature
Detailed Description
Schizophrenia is a chronic psychiatric disorder with a lifetime prevalence of 4.0 per 1,000. The introduction of antipsychotic medications in the 1950s resulted in marked clinical improvement in the symptom profile of schizophrenia, nevertheless the disease still contributes to a significant proportion of global disease burden in terms of both morbidity and mortality. In this regard, cognitive deficits and residual negative symptoms are considered major contributing factors to psychosocial disability and poor functional outcome associated with the disorder. Higher-order cognitive functions; e.g. working memory and executive functions; show variable deficits and are considered a core clinical symptom of schizophrenia. On the other hand, the disorder is also characterized by abnormalities at the basic level of primary sensory processing, i.e. auditory, visual and somatosensory processing. Such abnormalities in the primary process of sensory perception could change the sensory experiences of schizophrenia patients and thus contribute to the psychopathology. Event-related potentials (ERPs) are the neurophysiological correlates of sensory processing. ERP abnormalities have been widely described in schizophrenia literature: Pre-pulse inhibition of startle (PPI) in which a weaker pre-stimulus (pre-pulse) inhibits the reaction to a subsequent strong startling stimulus (pulse) is impaired in schizophrenia. P50 suppression, a measure of sensory gating, is also often absent or reduced in the disorder. N100; a measure of basic auditory sensory perception; shows significant amplitude reduction in patients compared to controls. Mismatch negativity (MMN), a measure of automatic deviance detection and shows characteristic attenuation in schizophrenia. P300, which is involved in higher-level stimulus evaluation and categorization, also shows abnormalities along the disease course. In the study by Clapp et al., 2005, auditory high frequency stimulation (tetanizing stimulation) resulted in an increase in auditory-evoked potentials (AEPs) in healthy individuals; i.e. an increase in N1 amplitude that persisted even after stimulation. This augmentation of N1 amplitude was regarded as a result of plastic synaptic potentiation similar to long-term potentiation (LTP) described after electrical tetanic stimulation in cellular studies. Similar findings were later replicated by Lei et al., 2017, where they used pure tones, narrow band noises and white noise to induce stable potentiation and augmentation of N1 amplitude.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Schizophrenia TS+ve
Arm Type
Experimental
Arm Description
Schizophrenia patients who receive auditory high frequency Tetanizing Stimulation
Arm Title
Schizophrenia TS-ve
Arm Type
Sham Comparator
Arm Description
Schizophrenia patients who receive sham comparator
Arm Title
Control TS+ve
Arm Type
Experimental
Arm Description
Healthy controls who receive auditory high frequency Tetanizing Stimulation
Arm Title
Control TS-ve
Arm Type
Sham Comparator
Arm Description
Healthy controls who receive sham comparator
Intervention Type
Diagnostic Test
Intervention Name(s)
Auditory High Frequency Tetanizing Stimulation
Intervention Description
50 ms tone pips presented at high frequency for 120 seconds
Intervention Type
Diagnostic Test
Intervention Name(s)
Sham Comparator
Intervention Description
auditory tone pips with interstimulus interval (ISI) 1 sec
Primary Outcome Measure Information:
Title
N100 wave (AEP) amplitude in µv [microvolts]
Description
N100 or N1 is a large, negative-going evoked potential measured by electroencephalography. It peaks in adults between 80 and 120 milliseconds after the onset of a stimulus, and distributed mostly over the fronto-central region of the scalp.
Time Frame
1-2 hours
Title
P300 wave amplitude in µv [microvolts] (auditory odd-ball task)
Description
The P300 (P3) wave is an event related potential (ERP) component elicited in the process of decision making. It is considered to be an endogenous potential, as its occurrence links not to the physical attributes of a stimulus, but to a person's reaction to it. More specifically, the P300 is thought to reflect processes involved in stimulus evaluation or categorization.
Time Frame
1-2 hours
Secondary Outcome Measure Information:
Title
performance of Wisconsin Card Sorting test (WCST).
Description
Wisconsin Card Sorting Test (WCST) is a neuropsychological test of "set-shifting", i.e. the ability to display flexibility in the face of changing schedules of reinforcement.
Time Frame
3 days

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
For Schizophrenia group: Inclusion Criteria: Able to give written informed consent Males (ages 20-50 years) Diagnosis of schizophrenia as confirmed by Structured Clinical Interview for DSM-V-TR (SCID) on stable doses of antipsychotic medications for at least 15 days scores 4 or more on at least one item of the Positive and Negative Syndrome Scale. Exclusion Criteria: History of / or current medical/neurological illnesses e.g. mental retardation (DSM-V) or epilepsy or significant head trauma Any type of hearing deficit will be excluded by audiometry assessment Substance abuse in the past 2 months medical conditions that make it difficult for the patient to visit the clinic in the designed schedule. For control group: Inclusion criteria: able to give written informed consent males (ages 20-50). Exclusion criteria: History of / or current medical/neurological illnesses e.g. mental retardation (DSM-V) or epilepsy or significant head trauma Any type of hearing deficit if they meet any axis-I diagnosis according to DSM-V confirmed by SCID. scores 2 or more on one item of the Positive and Negative Syndrome Scale
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ola O Shahin, MD
Organizational Affiliation
Department of Psychiatry-University of Cairo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Vishwajit L Nimgaonkar, PhD
Organizational Affiliation
Department of Psychiatry-University of Pittsburgh
Official's Role
Study Director
Facility Information:
Facility Name
Department of Psychiatry-Faculty of medicine-University of Cairo
City
Cairo
State/Province
Cairo Governerate
ZIP/Postal Code
11562
Country
Egypt

12. IPD Sharing Statement

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Trial of Stimulus-response Potentiation in Schizophrenia

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