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Completed

NCT Number: NCT00372151

L-Theanine in the Management of Schizophrenia

The aim of the proposed study is to investigate the efficacy and safety of add-on gamma-glutamylethylamide (L-theanine) versus a placebo for antipsychotic treatment for 8 weeks in a randomized, double-blind, parallel group study of 60 patients with schizophrenia and schizoaffective disorders.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Be'er Sheva Mental Health Center, Beersheba, Israel

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About this study

This is a two-year randomized placebo-controlled double-blind investigation of the use of augmentative L-theanine in the management of 60 patients with schizophrenia and schizoaffective disorders. We will investigate several outcome variables in these patients including the positive and negative symptoms, affective features, emotional distress, neuropsychological testing, side effects, and the quality of life. Participating subjects on stable antipsychotic treatment will be randomized to receive for 8 weeks either L-theanine (400 mg/day) or a placebo in addition to regular ongoing antipsychotic medication for 8 weeks. Subjects will be assessed at baseline and after 2, 4, 6, and 8 weeks of treatment using psychiatric rating scales, self-reported questionnaires, and a neuropsychological battery of tests. The efficacy and safety of augmenting antipsychotic treatment with L-theanine will be analyzed.

The Cambridge Neuropsychological Test Automated Battery (CANTAB) will be administered at commencement and completion of the study. The CANTAB battery consists of a series of interrelated computerized tests of visual and movement skills, attention and memory, and executive function, administered via a touch sensitive screen. The nonverbal nature of the CANTAB tests makes them largely language independent and culture free. These tests are run on an IBM-compatible personal computer with a touch-sensitive screen. Neuropsychological testing lasts approximately 2 hours. Subjects complete the tests in a fixed order with a break half-way through the testing session. For a description of the nature of these tests, the performance measures used, and how the test scores are derived, see (http://www.cantab.com/cantab/site/home.acds). The neuropsychological tests are categorized onto five cognitive domains: visual and movement skills, attention, memory, learning, sustained attention, and executive function: Motor Screening, Big/Little Circle, Reaction Time, Matching to Sample Visual Search, Delayed Matching to Sample, Pattern Recognition Memory, Spatial Recognition Memory, Spatial Span, Rapid visual information processing, Spatial working memory, Intra/Extra Dimensional Set Shift, and Stockings of Cambridge. In addition to raw scores from these tasks, the average value of the z-scores of the CANTAB neurocognitive tasks will be used to determine cognitive indices in specific domains.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-60 years, men or women
  • DSM-IV criteria for schizophrenia or schizoaffective disorder
  • At least 4 on the Clinical Global Impression Scale
  • At least two weeks of ongoing treatment with current antipsychotic agents.
  • Ability and willingness to sign an informed consent form for participation in the study.

Exclusion criteria

  • Evidence of serious neurologic or endocrine disorder, for example severe head trauma, seizure disorder, dementia, Cushings disease, or thyroid disorder, mental retardation, alcohol or drug abuse.
  • Renal disease
  • Hepatic dysfunction
  • Pregnant women
  • Patients receiving mood stabilizing medications.

Treatment and study plan

L-theanine

Dietary Supplement

400 mg/day, caps.

Placebo

Other

caps.

Primary outcomes

  1. The Clinical Global Impression Scale

    Time frame: every two weeks

  2. The Positive and Negative Syndrome Scale

    Time frame: every two weeks

  3. The Scale for the Assessment of Negative Symptoms

    Time frame: every two weeks

  4. The Calgary Depression Scale for Schizophrenia

    Time frame: every two weeks

  5. The Hamilton Scale for Anxiety

    Time frame: every two weeks

  6. Cambridge Neuropsychological Test Automated Battery (CANTAB)

    Time frame: every 4 weeks

Secondary outcomes

  1. The Global Assessment of Functioning

    Time frame: every two weeks

  2. The Talbieh Brief Distress Inventory

    Time frame: every two weeks

  3. The State/Trait Anxiety Inventory

    Time frame: every two weeks

  4. The Quality of Life Scale

    Time frame: every two weeks

  5. The Quality of Life Enjoyment and Satisfaction Questionnaire

    Time frame: every two weeks

  6. The Extrapyramidal Symptom Rating Scale

    Time frame: every two weeks

  7. Barnes Akathisia Scale

    Time frame: every two weeks

Sponsors and collaborators

Lead sponsor

Sha'ar Menashe Mental Health Center

Other

Collaborators

  • Beersheva Mental Health Center
  • Stanley Medical Research Institute

Registry information

Official study title

The Value of Augmenting L-Theanine in the Management of Schizophrenia: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Sep 6, 2006
Registry last updated
Dec 16, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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