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A Clinical Trial Via Telepsychiatry of Complementary and Alternative Treatments for the Management of Emotional Dysregulation in Youth

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ClinicalTrials.gov Identifier: NCT03911414
Recruitment Status : Not yet recruiting
First Posted : April 11, 2019
Last Update Posted : April 11, 2019
Sponsor:
Information provided by (Responsible Party):
Janet Wozniak, MD, Massachusetts General Hospital

Brief Summary:
This study consists of a 6-week, open-label, randomized clinical trial study to compare efficacy and tolerability of the natural treatments omega-3 fatty acids, inositol, and N-acetylcysteine (NAC) in the treatment of mood dysregulation in children and adolescents (ages 5-17). Subjects will be randomized to one of two arms: 1) omega-3 fatty acids plus inositol or 2) NAC.

Condition or disease Intervention/treatment Phase
Mood Disturbance Mood Disorders Natural Supplements Alternative Treatment Drug: Open-label Treatment with Omega-3 Fatty Acids + Inositol Drug: Open-label Treatment with N-Acetyl Cysteine Phase 4

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-Label Clinical Trial Conducted Via Telepsychiatry of Complementary and Alternative Treatments (Omega-3 Fatty Acids and Inositol vs. N-acetylcysteine) for the Management of Emotional Dysregulation in Youth
Estimated Study Start Date : May 2019
Estimated Primary Completion Date : May 2021
Estimated Study Completion Date : May 2021

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Omega-3 Fatty Acids + Inositol
Subjects will be treated with 1500mg QAM + 1500mg QPM of Omega-3 Fatty acids and inositol based on weight (Subjects under 25kg: 80mg per kg, rounded down to the nearest 500mg; Subjects weighing 25kg or more: 1000mg QAM + 1000mg QPM).
Drug: Open-label Treatment with Omega-3 Fatty Acids + Inositol
Open-label Treatment with Omega-3 Fatty Acids + Inositol

Experimental: N-Acetyl Cysteine
Subjects will be treated with N-Acetyl Cysteine based on age (Subjects ages 5-12: 1800mg daily; Subjects ages 13-17: 2700 mg daily).
Drug: Open-label Treatment with N-Acetyl Cysteine
Open-label Treatment with N-Acetyl Cysteine




Primary Outcome Measures :
  1. Mean Change in the Parent-Young Mania Rating Scale (P-YMRS) Score [ Time Frame: Baseline to 6 Weeks ]
    The YMRS consists of 11 items rated on a scale from 0 (symptoms not present) to 4 (symptoms extremely severe). It is used to assess manic symptoms. The YMRS score ranges from 0-60. Questions are asked about the last week. This scale is generally accepted as the main outcome measure in studies of pediatric bipolar disorder and is linked directly to the core symptoms of mania.


Secondary Outcome Measures :
  1. Mean Change in the Parent-completed Children's Depression Inventory (CDI) [ Time Frame: Baseline to 6 Weeks ]
    The CDI consists of 27 items quantifying symptoms such as depressed mood, hedonic capacity, vegetative functions, self-evaluation, and interpersonal behaviors. Each item consists of three statements graded in order of increasing severity from 0 to 2; parents select the one that characterized their child's symptoms best during the past 1 week. The item scores are combined into a total depression score, which ranges from 0 to 54. A higher CDI score means a higher depressive state.

  2. Mean Change in the NIMH Clinical Global Improvement scale (CGI) [ Time Frame: Baseline to 6 Weeks ]
    The CGI is a measure of illness severity adapted for specific disorders. It allows rating of mania, depression and overall bipolar disorder illness, as well as other conditions frequently comorbid with bipolar disorder. The severity score ranges from 1 (normal, not at all ill) to 7 (among the most extremely ill patients). The improvement score ranges from 1 (very much improved) to 7 (very much worse).



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Ages Eligible for Study:   5 Years to 17 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female subjects, 5-17 years of age.
  • Current symptoms of emotional dysregulation as indicated by combined T-scores on the Child Behavior Checklist > 180 on the Anxiety/Depression + Aggression + Attention subscales.
  • Subjects and their caregivers must be English-speaking, and have a level of understanding sufficient to communicate intelligently with the investigator and study coordinator, and to cooperate with all tests and examinations required by the protocol.
  • Subjects and their caregivers must be willing and able to comply with all study procedures.
  • Each subject and his/her authorized legal representative must understand the nature of the study. The subject's authorized legal representative must sign an informed consent document and the subject must sign an informed assent document.
  • Subject must be able to swallow pills.
  • Subject must have access to a computer with a camera, speaker, microphone, and internet connection.

Exclusion Criteria:

  • Investigator and his/her immediate family; defined as the investigator's spouse, parent, child, grandparent, or grandchild.
  • Serious or unstable illness including hepatic, renal, gastroenterological, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic disease.
  • History of bleeding diathesis, including those with von Willebrand disease.
  • Uncorrected hypothyroidism or hyperthyroidism.
  • History of sensitivity to omega-3 fatty acids, inositol or NAC. A non-responder or history of intolerance to omega-3 fatty acid, inositol or NAC after 2 months of treatment at adequate doses as determined by the clinician.
  • Severe allergies or multiple adverse drug reactions.
  • Unstable or untreated seizure disorder.
  • DSM-IV substance use, abuse or dependence.
  • Judged clinically to be at serious suicidal risk or C-SSRS score ≥ 4.
  • Current diagnosis of schizophrenia.
  • Current diagnosis or symptoms of psychosis.
  • IQ < 70.
  • Pregnant or nursing.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03911414


Contacts
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Contact: Abigail Farrell, BS 617-643-6617 aefarrell@partners.org
Contact: Elizabeth Noyes, BA 617-726-4651 enoyes@partners.org

Locations
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United States, Massachusetts
Massachusetts General Hospital Not yet recruiting
Boston, Massachusetts, United States, 02114-2696
Contact: Abigail Farrell, BS    617-643-6617    aefarrell@partners.org   
Contact: Elizabeth Noyes, BA    617-726-4651    enoyes@partners.org   
Principal Investigator: Janet Wozniak, MD         
Sponsors and Collaborators
Massachusetts General Hospital
Investigators
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Principal Investigator: Janet Wozniak, MD Massachusetts General Hospital

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Responsible Party: Janet Wozniak, MD, Director of the Pediatric Bipolar Disorder Clinical and Research Program, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT03911414     History of Changes
Other Study ID Numbers: 2019P00846
First Posted: April 11, 2019    Key Record Dates
Last Update Posted: April 11, 2019
Last Verified: April 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Inositol
Mood Disorders
Mental Disorders
Acetylcysteine
N-monoacetylcystine
Vitamin B Complex
Vitamins
Micronutrients
Nutrients
Growth Substances
Physiological Effects of Drugs
Antiviral Agents
Anti-Infective Agents
Expectorants
Respiratory System Agents
Free Radical Scavengers
Antioxidants
Molecular Mechanisms of Pharmacological Action
Protective Agents
Antidotes