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
About this trial
This is an interventional treatment trial for Autism
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
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
NCT ID
NCT00584480
First Posted
December 22, 2007
Last Updated
August 1, 2012
Sponsor
University of California, San Francisco
Collaborators
University of California, Davis
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
Learn more about this trial
Pilot Study of the Effect of Hyperbaric Oxygen Treatment on Behavioral and Biomarker Measures in Children With Autism
We'll reach out to this number within 24 hrs