Pilot Study to Improve Access to Early Intervention for Autism in Africa
NCT ID: NCT02751957
Last Updated: 2020-08-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
26 participants
INTERVENTIONAL
2016-07-01
2020-07-31
Brief Summary
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Detailed Description
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The site of the proposed study is the Center for Autism Research in Africa at the University of Cape Town (Director, Prof Petrus de Vries). South Africa offers a unique opportunity to study interactions among treatment, child, family, community and context, which act as facilitators or barriers of intervention implementation, thus providing preliminary information that could help match the right treatment to the right child and family. In a recent multisite P-ESDM RCT Estes and colleagues reported that that this parent coaching intervention helped to maintain parental adjustment directly after a child was diagnosed with ASD. However, the numbers of negative life events were a significant predictor of parenting stress and sense of competence. Child and caregiver factors, particularly prevalent in South Africa (eg. poverty, malnutrition, HIV/AIDS), are known to affect child cognitive and social-emotional development, as well as parenting stress. Gathering data on the feasibility and impact of a scalable early ASD intervention in an environment where other significant child and caregiver contextual challenges exist, offers a unique opportunity to examine broader contextual factors affecting intervention implementation. The investigator will therefore document the effects of broader contextual factors (for e.g. caregiver mental health, negative life events, HIV/AIDS, and poverty) on treatment impact. In addition, this study will further the understanding of how to implement mental health early interventions in a low and middle-income country (LMIC) context, by examining processes used to train and supervise non-specialist providers who will provide the caregiver coaching in this context.
The long term goal of this proposal is to advance understanding of affordable, sustainable early intervention strategies for developmental disorders, including ASD that would benefit all families regardless of resource availability.
Specific Aim #1: Adapt the P-ESDM treatment manual and training approach. P-ESDM is a brief, scalable caregiver-mediated early autism intervention.
Specific Aim #2: Pre-pilot the adapted P-ESDM training and intervention and refine methodological details of the experimental protocol. This will provide information on the structure, content, and feasibility of the adapted P-ESDM intervention and training approach.
Specific Aim #3: Pilot of the adapted P-ESDM with preschool aged children with ASD exploring the impact on: a) child social communication abilities and overall developmental outcome, and b) implementation outcomes.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Intervention
Receives caregiver coaching version of the Early Start Denver Model (ESDM) intervention, delivered by non-specialist workers. ESDM is an evidence based, behavioral intervention for young children who have an autism spectrum disorder. It is a behavioral treatment informed by the principles of applied behavior analysis.
Early Start Denver Model
The Early Start Denver Model is an evidence based, behavioral intervention for young children who have an autism spectrum disorder. It is a behavioral treatment informed by the principles of applied behavior analysis.
Interventions
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Early Start Denver Model
The Early Start Denver Model is an evidence based, behavioral intervention for young children who have an autism spectrum disorder. It is a behavioral treatment informed by the principles of applied behavior analysis.
Eligibility Criteria
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Inclusion Criteria
* a caretaker who speaks isiXhosa, Afrikaans or English
* lives within an area served by the Red Cross Neurodevelopmental clinic;
* willing to participate in the intervention and be randomized to the intervention or control group.
Exclusion Criteria
* significant sensory or motor impairment (e.g. cerebral palsy)
* major physical problems
* uncontrolled seizures
* IQ below 35 as measured by mean age equivalence score on the Griffiths Scales of Mental Development
* unable to attend 3 assessments and 12, 1-hour, weekly consecutive intervention sessions.
18 Months
72 Months
ALL
No
Sponsors
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University of Cape Town
OTHER
Duke University
OTHER
Responsible Party
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Principal Investigators
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Lauren Franz, MBChB
Role: PRINCIPAL_INVESTIGATOR
Duke University
Locations
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University of Cape Town
Cape Town, Western Cape, South Africa
Countries
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Other Identifiers
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Pro00064533
Identifier Type: -
Identifier Source: org_study_id
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