Transcranial Direct Current Stimulation (tDCS) to Improve Gesture Control

NCT ID: NCT03463902

Last Updated: 2024-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-29

Study Completion Date

2024-03-22

Brief Summary

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The majority of schizophrenia patients is impaired in hand gesture performance, which contributes to poor functional outcome and poor communication skills. The left inferior frontal gyrus (IFG) and the left inferior parietal lobe (IPL) are key nodes of the gesture network, which is less active in patients with schizophrenia. Here, the investigators test single 10 min sessions of tDCS known to either enhance or inhibit local brain activity for app. 1 hour. The investigators aim to determine, which protocol may improve gesture performance in patients and healthy controls. This is a randomized, double-blind, cross-over, placebo-controlled single-center trial in 20 patients with schizophrenia spectrum disorders and 20 healthy controls. Gesture performance will be tested immediately after each tDCS session, which are separated by 24 hours. Results of this study will inform larger interventional trials comparing 2 tDCS protocols with repeated administration.

Detailed Description

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Schizophrenia is associated with poor social functioning, which is perturbed by deficits in social interaction including nonverbal communication. The use of hand gestures is critical for nonverbal communication, but the majority of schizophrenia patients has severe gesture impairments. Today no intervention may ameliorate gesture impairments.

Patients with gesture impairments have altered structure and function of the gesture network, particularly the left inferior frontal gyrus (IFG) and also the left inferior parietal lobe (IPL). Noninvasive brain stimulation techniques may alter local brain function. Transcranial direct current stimulation (tDCS) for 10 mins is a very safe method to alter brain states locally for a period of 1-2 hours. Indeed, facilitatory stimulation of the left frontal cortex by tDCS demonstrated improved gesture perception and interpretation in healthy subjects. Furthermore, patients with apraxia identified gestures better after facilitatory tDCS over the left inferior parietal lobe (IPL). Thus, the investigators hypothesize that local changes of brain activity within the gesture network would change gesture performance.Particularly, anodal (facilitatory) stimulation of the left IFG would improve gesture performance. The investigators will test single sessions of tDCS in healthy subjects and schizophrenia patients. If one of the protocols proves to have superior effects, this result will help to plan interventional trials targeting social interaction deficits in schizophrenia.

The aim of the study is to determine the effect of one 10 min session of anodal tDCS over the left IFG on gesture performance compared to three active and one placebo tDCS sessions. This is a randomized, double-blind, cross-over, placebo-controlled single-center trial in 20 patients with schizophrenia spectrum disorders and 20 healthy controls. After baseline assessment of gesture performance, participants will receive one 10 min tDCS protocol each day, immediately followed by assessments of gesture performance and dexterity. Gesture performance will be measured with video recorded Test of Upper Limb Apraxia, which is rated blindly according to a manual. Active comparisons are cathodal tDCS over left IFG, anodal tDCS over left IPL and cathodal tDCS over left IPL.

Conditions

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Schizophrenia and Related Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

randomized, double-blind, cross-over trial of 5 tDCS protocols
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors
participants, outcome assessors and raters are blinded. tDCS application is performed by an unblinded investigator

Study Groups

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left IFG anodal

2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Group Type EXPERIMENTAL

left IFG anodal

Intervention Type DEVICE

Single session of transcranial direct current stimulation (tDCS) over left IFG anodal stimulation

2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

left IFG cathodal

2 mA Stimulation of 10 min, cathodal electrode over left IFG, anodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Group Type ACTIVE_COMPARATOR

left IFG cathodal

Intervention Type DEVICE

Single session of transcranial direct current stimulation (tDCS) over left IFG cathodal stimulation

2 mA Stimulation of 10 min, cathodal electrode over left IFG, anodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

left IPL anodal

2 mA Stimulation of 10 min, anodal electrode over left IPL, cathodal electrode over right IPL, 30 sec ramp to start and 30 sec ramp to stop

Group Type ACTIVE_COMPARATOR

left IPL anodal

Intervention Type DEVICE

Single session of transcranial direct current stimulation (tDCS) over left IPL anodal stimulation 2 mA Stimulation of 10 min, anodal electrode over left IPL, cathodal electrode over right IPL, 30 sec ramp to start and 30 sec ramp to stop

left IPL cathodal

2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Group Type ACTIVE_COMPARATOR

left IPL cathodal

Intervention Type DEVICE

Single session of transcranial direct current stimulation (tDCS) over left IPL cathodal stimulation 2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Placebo

anodal electrode over left IFG, cathodal electrode over right IFG, stimulation only during 30 sec ramp at beginning and end of 10 min

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DEVICE

Single session of placebo tDCS over left IFG 10 min duration, 30 sec ramp during start and end

Interventions

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left IFG anodal

Single session of transcranial direct current stimulation (tDCS) over left IFG anodal stimulation

2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Intervention Type DEVICE

left IFG cathodal

Single session of transcranial direct current stimulation (tDCS) over left IFG cathodal stimulation

2 mA Stimulation of 10 min, cathodal electrode over left IFG, anodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Intervention Type DEVICE

left IPL anodal

Single session of transcranial direct current stimulation (tDCS) over left IPL anodal stimulation 2 mA Stimulation of 10 min, anodal electrode over left IPL, cathodal electrode over right IPL, 30 sec ramp to start and 30 sec ramp to stop

Intervention Type DEVICE

left IPL cathodal

Single session of transcranial direct current stimulation (tDCS) over left IPL cathodal stimulation 2 mA Stimulation of 10 min, anodal electrode over left IFG, cathodal electrode over right IFG, 30 sec ramp to start and 30 sec ramp to stop

Intervention Type DEVICE

Placebo

Single session of placebo tDCS over left IFG 10 min duration, 30 sec ramp during start and end

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Right handed according to the Edinburgh Handedness Inventory
* Ability and willingness to participate in the study
* Ability to provide written informed consent
* Informed Consent as documented by signature (Appendix Informed Consent Form)
* Spent majority of childhood/adolescence in Switzerland
* Patients: schizophrenia spectrum disorder according to DSM-5

Exclusion Criteria

* Women who are pregnant or breast feeding
* Metal objects on or in the body (e.g. grenade splinter, cardiac pacemaker, vessel clips, metal prostheses, contraceptive coil, cochlear implants, hearing aid, tooth implant)
* Tattoos on head, neck or shoulder in close proximity to the electrode placement
* Current skin problems on the scalp, eg. bruises or open wounds
* History of neurosurgery, any severe head wounds, history of neurologic disorders impacting gesture, e.g. Parkinson's disease, stroke, multiple sclerosis
* Active drug addiction except nicotine
* Known contact allergies
* Controls: first-degree relatives with schizophrenia spectrum disorders
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Bern

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sebastian Walther, MD

Role: PRINCIPAL_INVESTIGATOR

University of Bern, University Hospital of Psychiatry

Locations

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University Hospital of Psychiatry

Bern, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2017-01995

Identifier Type: -

Identifier Source: org_study_id

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