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Pilot Study of the Effect of Hyperbaric Oxygen Treatment on Behavioral and Biomarker Measures in Children With Autism (HBOT)

Primary Purpose

Autism

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Hyperbaric Oxygen Treatment (HBOT)
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autism

Eligibility Criteria

3 Years - 8 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of DSM-IV defined autism and meets cut off for autism on the Autism Diagnostic Inventory-Revised (ADI-R) or Social Communication Questionnaire (SCQ) and the Autism Diagnostic Observation Scale (ADOS).
  2. Age 3 to 8 years.
  3. Nonverbal IQ of 50 or above.
  4. Parental agreement to continue present dietary, behavioral or psychotropic drug treatment but not change treatment during 20 week intervention.

Exclusion Criteria:

  1. Clinical evidence of seizure disorder
  2. Active infection with fever
  3. Fragile X or other known genetic cause of autism
  4. Perinatal brain injury (e.g. cerebral palsy)
  5. Previous adequate trial (at least 20 session) of HBOT
  6. Inability to clear ears in the HBOT chambers

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Active Comparator

    Arm Label

    1

    Arm Description

    Active Hyperbaric Oxygen Treatment (HBOT)

    Outcomes

    Primary Outcome Measures

    Number of Participants With the Given Clinical Global Impression Scale - Improvement (CGI-I) Score
    Assessment of global changes in severity of autistic symptoms. CGI-I scores formulated by the clinician based on parent interview of changes in the child's behavior and from direct clinical observation, where scores of 0 = no improvement,1 = minimally improved, 2 = much improved, and 3 = very much improved.

    Secondary Outcome Measures

    Full Information

    First Posted
    December 22, 2007
    Last Updated
    August 1, 2012
    Sponsor
    University of California, San Francisco
    Collaborators
    University of California, Davis
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00584480
    Brief Title
    Pilot Study of the Effect of Hyperbaric Oxygen Treatment on Behavioral and Biomarker Measures in Children With Autism
    Acronym
    HBOT
    Official Title
    Pilot Study of the Effect of Hyperbaric Oxygen Treatment on Behavioral and Biomarker Measures in Children With Autism
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2007 (undefined)
    Primary Completion Date
    September 2009 (Actual)
    Study Completion Date
    September 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of California, San Francisco
    Collaborators
    University of California, Davis

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this study is to increase the understanding of the effect of Hyperbaric Oxygen Treatment (HBOT) on the behavior and functioning of children with autism. The main goal of this study is to demonstrate that HBOT is safe and tolerable in autistic children, and to measure the effect of HBOT on specific chemicals in their blood that may play a role in the child's behavior.
    Detailed Description
    During the study's 20-week duration, all children will receive Hyperbaric Oxygen Treatment (HBOT) for two eight-week sessions, with a four week session between. Therefore, all children will participate in the study for 20 weeks, and will receive HBOT for 16 weeks. This is an open label study. This means that there will not be a placebo group in the study. All study participants will receive the same treatment of HBOT in a hard shell chamber. Normal air contains about 24% oxygen at a pressure of about 1 atmosphere absolute (ATA). The chamber will contain 100 percent oxygen at a pressure of 1.5 ATA, which is equivalent to the pressure at a depth of 15 feet in sea water. Each subject will complete the first 40 treatments during one hour sessions on 5 separate days in each of the first 8 weeks. They will then take a 4-week break before they begin their next 40 treatments, which will also occur during one hour sessions on 5 separate days in each of the last 8 weeks. The entire study will last 20 weeks. The child's behavior will be measured and evaluated at the MIND Institute at the beginning of the study, at week 8, and at week 20.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    10 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Active Comparator
    Arm Description
    Active Hyperbaric Oxygen Treatment (HBOT)
    Intervention Type
    Other
    Intervention Name(s)
    Hyperbaric Oxygen Treatment (HBOT)
    Intervention Description
    1.5 ATA at 100% Oxygen of HBOT
    Primary Outcome Measure Information:
    Title
    Number of Participants With the Given Clinical Global Impression Scale - Improvement (CGI-I) Score
    Description
    Assessment of global changes in severity of autistic symptoms. CGI-I scores formulated by the clinician based on parent interview of changes in the child's behavior and from direct clinical observation, where scores of 0 = no improvement,1 = minimally improved, 2 = much improved, and 3 = very much improved.
    Time Frame
    Baseline, 8 Weeks from baseline, and 20 Weeks from baseline

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    3 Years
    Maximum Age & Unit of Time
    8 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of DSM-IV defined autism and meets cut off for autism on the Autism Diagnostic Inventory-Revised (ADI-R) or Social Communication Questionnaire (SCQ) and the Autism Diagnostic Observation Scale (ADOS). Age 3 to 8 years. Nonverbal IQ of 50 or above. Parental agreement to continue present dietary, behavioral or psychotropic drug treatment but not change treatment during 20 week intervention. Exclusion Criteria: Clinical evidence of seizure disorder Active infection with fever Fragile X or other known genetic cause of autism Perinatal brain injury (e.g. cerebral palsy) Previous adequate trial (at least 20 session) of HBOT Inability to clear ears in the HBOT chambers
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Robert L Hendren, DO
    Organizational Affiliation
    University of California, Davis - M.I.N.D. Institute
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    21818676
    Citation
    Bent S, Bertoglio K, Ashwood P, Nemeth E, Hendren RL. Brief report: Hyperbaric oxygen therapy (HBOT) in children with autism spectrum disorder: a clinical trial. J Autism Dev Disord. 2012 Jun;42(6):1127-32. doi: 10.1007/s10803-011-1337-3.
    Results Reference
    derived

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    Pilot Study of the Effect of Hyperbaric Oxygen Treatment on Behavioral and Biomarker Measures in Children With Autism

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