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Trial registered on ANZCTR
Registration number
ACTRN12611000722998
Ethics application status
Approved
Date submitted
11/07/2011
Date registered
12/07/2011
Date last updated
30/09/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Healthy Eating Learning Program (HELP) Study for Children with Autism Spectrum Disorder
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Scientific title
In children with Autism Spectrum Disorder and feeding difficulties, is traditional operant conditioning intervention more effective than novel systematic desensitisation intervention at improving dietary variety and nutrition, and decreasing maladaptive mealtime behaviours and parental stress?
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Secondary ID [1]
262257
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Nil
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Universal Trial Number (UTN)
U1111-1121-7588
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Trial acronym
HELP study for children with ASD
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Autism Spectrum Disorder
267954
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Feeding Difficulties
267988
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Condition category
Condition code
Mental Health
268092
268092
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0
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Autistic spectrum disorders
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Diet and Nutrition
268093
268093
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0
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Other diet and nutrition disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Arm One: One-on-one behaviour modification therapy Run in an individual session for 1 hour per week over ten weeks (weekly schedule) or 10 times over one week (intensive schedule) Involves providing a verbal prompt to encourage consumption of spoonfuls of new food/s, with positive reinforcement (verbal and/or with toys etc) upon consumption of these foods. Parents initially observe from behind a one-way mirror and assist in collecting information about the behaviours they are observing in their child. As sessions continue, parents are transitioned into the room, and are trained to offer new foods and provide positive reinforcement by the end of the therapy block. Parents also receive standardised information about nutrition, behaviour management and feeding development. Arm Two: Systematic desensitisation therapy Run in an individual session for 1 hour per week over ten weeks (weekly schedule) or 10 times in one week (intensive schedule) Involves the child being exposed to gradually more challenging modelling and play with food (based on a sensory hierarchy of look>touch>smell>taste). Parents initially observe the sessions from behind a one-way mirror with a second therapist and assist in observing transitions and reactions in their children. As the block continues, parents are rotated in and out of the room to assist in modelling play using the sensory hierarchy. Parents also receive standardised information about nutrition, behaviour management and feeding development.
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Intervention code [1]
266649
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Behaviour
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Intervention code [2]
266650
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Treatment: Other
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Comparator / control treatment
Natural control will be waiting for therapy. These children will either be offered input via an intensive schedule (as described above) or during a subsequent 10-week block. As recruitment for this study will occur in an ongoing fashion, there will be multiple opportunities to access therapy if it is not immediately available.
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Control group
Active
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Outcomes
Primary outcome [1]
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Adequacy of diet and overall increase in dietary variety
Assessed via 3-day weighed food diary, modified Children's Dietary Questionnaire (Magarey et al. 1999)(food frequency questionnaire) and New Food Lists, where parents indicate in an ongoing fashion how many times their child is offered new foods and the number of acceptances or rejections
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Assessment method [1]
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Timepoint [1]
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Mid-intervention
Immediately post-intervention
3 months post-intervention
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Primary outcome [2]
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Growth (change in weight and height)
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Assessment method [2]
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Timepoint [2]
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Immediately post-intervention
3 months post-intervention
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Primary outcome [3]
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Change in fat-free mass as measured by body composition measures Measured via Bioelectrical Impedance Analysis and Total Body Potassium Measurement
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Assessment method [3]
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Timepoint [3]
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Immediately post-intervention
3 months post-intervention
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Secondary outcome [1]
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Improvement in mealtime behaviours (% desirable vs undesirable behaviours; mealtime duration)
Measured via Behaviour Pediatrics Feeding Assessment (Adapted from Crist et al. 2001), and self-developed HELP study: Eating Skills and Behaviours Questionnaire. Questionnaires involve parent-rated likert scales (parents rate level of concern).
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Assessment method [1]
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Timepoint [1]
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Immediately post-intervention
3 months post-intervention
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Secondary outcome [2]
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Improvement in mealtime interactions between parent and child
Measured via Dyadic Parent-Child Interaction Coding System (Revised) (Eyberg, 1994). A video-tape is taken of the parent interacting with their child in a non-food related activity, a parent offering their child a preferred food, and the parent offering their child a non-preferred food. All videos will be rated externally by the team psychologist who will not be working directly with the children involved.
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Assessment method [2]
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Timepoint [2]
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3 months post-intervention
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Secondary outcome [3]
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Improvement in parental stress (overall and mealtime specific)
Measured via self-developed HELP study: Parent percieved stress questionnaire and the Parenting Stress Index - Short Form.
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Assessment method [3]
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Timepoint [3]
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Immediately post-intervention
3 months post-intervention
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Secondary outcome [4]
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Increased interest in trying unfamiliar foods
Measured with Children's Picky Eating Questionnaire (Adapted from Carruth and Skinner, 2000) and New Foods Lists, where parents indicate in an ongoing fashion how many times their child is offered new foods and the number of acceptances or rejections.
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Assessment method [4]
276534
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Timepoint [4]
276534
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Immediately post-intervention
3 months post-intervention
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Eligibility
Key inclusion criteria
Children with a diagnosis of Autism Spectrum Disorder, or a pending diagnosis of Autism Spectrum Disorder
Limited dietary variety across core food groups: diet currently includes less than 10 foods which are predominantly carbohydrates, 10 foods which are predominantly proteins, and 10 fruits/vegetables; limited range of textures consumed; don’t eat an age-appropriate range of textures; limit diet to only 1 or 2 textures of foods; consume predominantly ‘easy-to-eat’ junk foods
Mealtimes are taking longer than 30 minutes
There are problematic behaviours at mealtimes, which are contributing to parental stress
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Minimum age
1
Years
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Maximum age
11
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Children who are medically unstable: this describes acutely unwell children who may experience a deterioration in health.
Children with documented aspiration on any solid food textures (children on modified liquids will be accepted)
Children with severe malnutrition, whose primary goal of nutrition could only be achieved by supplementary tube feeding
Children with gut malabsorption disorders, which are not well controlled or understood
Children with an allergy or current intolerance to more than 2 types of foods
Children whose primary health carer has a known/declared mental health condition
Children whose family’s primary language is that other than English or children identified as being of Aboriginal or Torres Strait Islander background
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Randomly generated numbers have been placed in sealed envelopes by a colleague who is not involved with the study. After children have received their initial assessment and are deemed eligible to receive intervention, the next envelope in the sequence will be opened.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A computer generated random number sequence will be used to allocate the numbers to sealed envelopes
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
Inter-rater reliability for assessments where 10% of video-taped assessments requiring objective scoring will be reviewed by a blind clinician.
Coders for dietary variety measures and parent-child interaction measures will be blinded.
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
5/09/2011
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Actual
5/09/2011
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Date of last participant enrolment
Anticipated
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Actual
22/02/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
101
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
4046
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4029
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Queensland Children's Medical Research Institute, Royal Children's Hospital
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Address [1]
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Queensland Children's Medical Research Institute
Level 4, Foundation Building, Royal Children's Hospital, Herston Road, Herston QLD 4029
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Country [1]
267138
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Australia
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Funding source category [2]
267139
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Self funded/Unfunded
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Name [2]
267139
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Jeanne Marshall
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Address [2]
267139
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Queensland Children's Medical Research Institute
Level 4, Foundation Building, Royal Children's Hospital, Herston Road, Herston Queensland 4029
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Country [2]
267139
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Australia
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Funding source category [3]
269778
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University
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Name [3]
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The University of Queensland
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Address [3]
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St. Lucia, Queensland 4068
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Country [3]
269778
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Australia
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Primary sponsor type
Hospital
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Name
Queensland Children's Medical Research Institute
Royal Children's Hospital
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Address
Level 4, Foundation Building, Royal Children's Hospital, Herston Road, Herston Queensland 4029
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Country
Australia
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Secondary sponsor category [1]
264214
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Government body
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Name [1]
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Queensland Health
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Address [1]
264214
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Health Research Fellowship for Dr. Pamela Dodrill
Speech Pathology Department
Royal Children's Hospital
Herston Road
Herston
Queensland
4029
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Country [1]
264214
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Australia
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Secondary sponsor category [2]
268820
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University
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Name [2]
268820
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The University of Queensland
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Address [2]
268820
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St. Lucia, Queensland 4068
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Country [2]
268820
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
269127
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Children's Health Services Human Research Ethics Committee (EC00175)
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Ethics committee address [1]
269127
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c/ Department of Paediatrics & Child Health Level 3, Foundation Building Royal Children's Hospital Herston Road HERSTON QLD 4029
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Ethics committee country [1]
269127
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Australia
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Date submitted for ethics approval [1]
269127
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10/05/2010
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Approval date [1]
269127
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12/05/2010
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Ethics approval number [1]
269127
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HREC/10/QRCH/30
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Ethics committee name [2]
269128
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Delete
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Ethics committee address [2]
269128
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Delete
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Ethics committee country [2]
269128
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Date submitted for ethics approval [2]
269128
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01/08/2010
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Approval date [2]
269128
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01/03/2011
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Ethics approval number [2]
269128
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1575C
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Ethics committee name [3]
269129
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University of Queensland Medical Research Ethics Committee
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Ethics committee address [3]
269129
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Human Ethics Unit The University of Queensland St. Lucia QLD 4068
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Ethics committee country [3]
269129
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Australia
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Date submitted for ethics approval [3]
269129
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10/05/2010
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Approval date [3]
269129
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12/05/2010
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Ethics approval number [3]
269129
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2010000677
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Summary
Brief summary
This study is a randomised controlled trial to evaluate the clinical benefits, and cost-effectiveness of two feeding treatment programs for children with ASD and feeding difficulties, including a restricted range of dietary intake (<30 foods across the food groups). Baseline assessment will include parent-completed questionnaires and on-site (Herston) feeding and growth assessments. There are two arms of intervention. Arm One is an individual behaviour modification program. Arm Two involves individual systematic desensitisation therapy. Both arms will involve parent education regarding nutrition and behaviour management for children with feeding difficulties. Intervention will be provided over two phases. Parents will elect to participate in weekly intervention (10 sessions over 10 weeks) or intensive intervention (10 sessions over one week).
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Trial website
www.qcmri.org.au
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Trial related presentations / publications
Blank
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Public notes
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Contacts
Principal investigator
Name
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Dr Pamela Dodrill
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Address
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Queensland Children's Medical Research Institute
Level 4, Foundation Building, Royal Children's Hospital
Herston Brisbane
Australia
4029
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Country
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Australia
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Phone
32658
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+61 7 3636 6107
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Fax
32658
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Email
32658
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[email protected]
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Contact person for public queries
Name
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Jeanne Marshall
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Address
15905
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Queensland Children's Medical Research Institute
Level 4, Foundation Building, Royal Children's Hospital, Herston Road, Herston Queensland 4029
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Country
15905
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Australia
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Phone
15905
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+61 7 3636 1290
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Fax
15905
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+61 7 3636 5578
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Email
15905
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[email protected]
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Contact person for scientific queries
Name
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Jeanne Marshall
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Address
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Queensland Children's Medical Research Institute
Level 4, Foundation Building, Royal Children's Hospital, Herston Road, Herston Queensland 4029
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Country
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Australia
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Phone
6833
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+61 7 3636 1290
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Fax
6833
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+61 7 3636 5578
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Email
6833
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Dimensions AI
Clinical Characteristics of 2 Groups of Children With Feeding Difficulties
2016
https://doi.org/10.1097/mpg.0000000000000914
N.B. These documents automatically identified may not have been verified by the study sponsor.
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