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Telehealth Intervention for Autism Spectrum Disorder

Primary Purpose

Autism Spectrum Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
OT4ASD
Sponsored by
Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Autism Spectrum Disorder

Eligibility Criteria

4 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Diagnosis of Autism Spectrum Disorder
  • Between the ages of 4 years 0 months and 12 years 0 months
  • Evidence of sensory symptoms based on the Sensory Processing Measure
  • Family is willing to participate
  • Physically able to participate in active, sensorimotor activities

Exclusion Criteria:

  • Primary (visual or auditory) uncorrected sensory deficits
  • Do not meet age or diagnostic criteria

Sites / Locations

  • Rose R. Kennedy Children's Evaluation and Rehabilitation Center (CERC) at MontefioreRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Feasibility trial group

Arm Description

One group (arm) trial where all will receive treatment.

Outcomes

Primary Outcome Measures

Daily Living Skills Change Score - Pediatric Evaluation of Disabilities Inventory
Change in daily living skills (on a scale of 0 to 25) measured with the Pediatric Evaluation of Disabilities Inventory. Change score range 0-25; higher score means better outcome.
Pervasive Developmental Disorders Behavioral Inventory T Score Autism Behaviors
Change is autism behaviors and sensory approach behaviors. Raw scores are converted to T Score. Minimum = 10 Maximum = 80

Secondary Outcome Measures

Goal Attainment Scale T Score
Rating of individual goals. Rating Scale -2 to +2 is converted to T-Score; higher score means better outcome.
Sensory Processing Measure
Change in sensory hypo or hyper reactivity. T scores range from 40 to 80; Lower score means better outcome.

Full Information

First Posted
March 24, 2021
Last Updated
June 1, 2023
Sponsor
Thomas Jefferson University
Collaborators
Montefiore Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04832152
Brief Title
Telehealth Intervention for Autism Spectrum Disorder
Official Title
Testing the Feasibility of a Teletherapy Plus Parent Coaching Intervention for Children With Autism
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Thomas Jefferson University
Collaborators
Montefiore Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Autism Spectrum Disorder (ASD) is one of the most frequently occurring childhood-onset neurodevelopmental disorders affecting 1 in every 54 children. Most children with ASD experience challenges participating in daily activities (e.g.: eating, sleeping, bathing, grooming, playing, etc.) and receive occupational therapy intervention to address these. The COVID-19 pandemic has restricted in-person therapy for many of these children and there is an urgent need for evidence-based, validated telehealth intervention. This project will adapt an evidence-based occupational therapy intervention, termed OT4ASD to a telehealth delivery model. The aims of the project are to: 1) adapt the existing intervention protocol to a telehealth delivery model, 2) train therapists and evaluate the therapist's ability to conduct OT4ASD, 3) determine if OT4ASD delivered via the telehealth is acceptable and feasible to parents and interventionists; and 4) whether children improve in the daily living skills. OT4ASD follows a systematic protocol and uses active, individually-tailored sensory motor activities that are specifically designed to address the child's needs. The investigators believe this will be the first telehealth manualized protocol to address the sensory motor symptoms of ASD and measure outcomes at the daily life activity and participation levels.
Detailed Description
Autism Spectrum Disorder (ASD) is one of the most frequently occurring childhood-onset neurodevelopmental disorders affecting 1 in every 54 children1. As a lifelong condition, individuals with ASD experience a range of intellectual, behavioral, sensory, motor, and functional challenges that impact successful participation in daily life activities and tasks. As a result, occupational therapy (OT) intervention is a frequently requested and utilized service in ASD, and clinically validated OT approaches are needed. In a series of studies funded by the NIH and autism foundations, our team manualized and studied an OT intervention that targets the sensory and motor factors impacting participation in daily life activities and tasks and showed significant improvements in those that received the intervention in comparison to controls 2-4. In this project, the investigators plan to adapt our existing protocol to a telehealth model of service delivery, and evaluate its feasibility and preliminary effectiveness. The COVID-19 global pandemic created a call to action for healthcare providers to design unique and innovative methods for therapeutic service delivery. This shift creates an urgent need for remote solutions so that therapeutic services can be delivered in safely and effectively. Since the onset of the COVID-19 pandemic, families have reported regression in adaptive functioning in addition to a negative impact on social skills and increased anxiety, and an impact to daily routines of children with ASD5. In a recent survey of families with children with ASD, 95% of the parents reported that disruptions in services/therapies negatively impacted their child's behaviors and only 35% of families were receiving telehealth services/therapies6. To address these increased needs for children with ASD and to meet the need of manualized telehealth intervention, the investigators propose to adapt the existing intervention to a telehealth delivery model. This intervention, termed occupational therapy for children with Autism Spectrum Disorder (OT4ASD) targets the sensory motor factors that impact behavior and participation in life activities and tasks. This project is significant in that it will address the need for evidence-based OT services for children with ASD using an innovative telehealth model. Given that many children with ASD require treatment for the sensory and motor symptoms that impact their optimal participation in a range of daily life activities and tasks, and that the current COVID 19 pandemic has compromised access to this therapy, this project is urgently needed. Innovation: Telehealth offers an emerging and innovative approach for OT intervention. Research shows that children with ASD require intensive intervention to assure best outcomes and telehealth offers an innovative solution for providing therapy during a pandemic. To the investigator's knowledge, this will be the first telehealth manualized protocol to address the sensory motor symptoms of ASD and measure outcomes at the activity and participation levels of the ICF framework. Importantly, the investigators will adapt an evidence-based, manualized intervention with solid data on outcomes to a telehealth model. The protocol will operationalize the data-driven decision making (DDDM) approach into an on-line format. DDDM is innovative in that it explicitly guides the therapist to contextualize intervention within the child and family's real life participation challenges and use data from assessment to individualize the intervention. DDDM measures outcomes at the proximal (sensory and motor factors) and distal (functional/participation-based goals) levels facilitating an intervention that is context-specific and participation-oriented. Methods: The project will first adapt the existing protocol into a telehealth delivery model using a formative approach that includes a modified Delphi process to obtain input and consensus from experts in telehealth and autism interventions and key stakeholders (parents and clinical interventionists). Next, the investigators will conduct a feasibility trial to assess the acceptability, satisfaction and implementation fidelity as well as gather data on clinically meaningful outcomes. Outcomes will be measured at the proximal and distal levels using validated outcome measures to assure information gained is relevant and scientifically rigorous. Data from the feasibility trial will be used to support an R01 application to conduct a randomized trial of OT4ASD. To implement the project, the investigators utilize a highly skilled team of clinicians and scientists with experience in conducting randomized trials in autism who will work collaboratively to translate knowledge gained into useful information that will impact the lives of families and children with ASD. Our approach is consistent with contemporary models of evidence-based practice and rehabilitation science promoting promote high integrity, evidence-based information from research that targets relevant and meaningful areas for each child and family. The timeline is ambitious and the investigators feel well-equipped to meet it given past experiences and expertise. In summary, this project addresses an urgent need to provide rehabilitation services to children with ASD using remote technology. It will operationalize best practices in telehealth to adapt an existing evidence-based OT intervention and utilize a skilled and experienced team of investigators. As such, this project is consistent with the AACPDM mission to promote excellence in research and services for persons with childhood-onset disabilities.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The purpose of this project is to adapt an existing, evidence-based occupational therapy intervention for children with ASD to a telehealth delivery model. The main objectives of the project are to 1) adapt the manual so that it operationalizes best-practices of occupational therapy telehealth50,51, 2) test its feasibility, and 3) evaluate preliminary outcomes. Design: In the formative research aspect of this project will use survey methodology and a modified Delphi process to adapt our current intervention to a telehealth delivery model (Aim 1). In Aim 2 we will conduct a feasibility trial (Figure 2) to assess therapists' fidelity, participant recruitment and retention, acceptability of the protocol by parents and therapists, and clinically meaningful differences.
Masking
None (Open Label)
Masking Description
none. This is a feasiblity trial
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Feasibility trial group
Arm Type
Other
Arm Description
One group (arm) trial where all will receive treatment.
Intervention Type
Other
Intervention Name(s)
OT4ASD
Intervention Description
Occupational therapy will focus on education and coaching of families/caregivers of children with autism spectrum disorder to help them adapt their daily routines to address their child's sensory needs.
Primary Outcome Measure Information:
Title
Daily Living Skills Change Score - Pediatric Evaluation of Disabilities Inventory
Description
Change in daily living skills (on a scale of 0 to 25) measured with the Pediatric Evaluation of Disabilities Inventory. Change score range 0-25; higher score means better outcome.
Time Frame
up to 14 weeks
Title
Pervasive Developmental Disorders Behavioral Inventory T Score Autism Behaviors
Description
Change is autism behaviors and sensory approach behaviors. Raw scores are converted to T Score. Minimum = 10 Maximum = 80
Time Frame
up to 14 weeks
Secondary Outcome Measure Information:
Title
Goal Attainment Scale T Score
Description
Rating of individual goals. Rating Scale -2 to +2 is converted to T-Score; higher score means better outcome.
Time Frame
up to 14 weeks
Title
Sensory Processing Measure
Description
Change in sensory hypo or hyper reactivity. T scores range from 40 to 80; Lower score means better outcome.
Time Frame
up to 14 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosis of Autism Spectrum Disorder Between the ages of 4 years 0 months and 12 years 0 months Evidence of sensory symptoms based on the Sensory Processing Measure Family is willing to participate Physically able to participate in active, sensorimotor activities Exclusion Criteria: Primary (visual or auditory) uncorrected sensory deficits Do not meet age or diagnostic criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Roseann C Schaaf, PhD
Phone
6102912179
Email
roseann.schaaf@jefferson.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Rachel L Dumont, M.S.
Phone
6107641035
Email
rachel.dumont@jefferson.edu
Facility Information:
Facility Name
Rose R. Kennedy Children's Evaluation and Rehabilitation Center (CERC) at Montefiore
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elizabeth C Ridgway, OTD
Phone
718-839-7101
Email
elizabeth.ridgway@einsteinmed.org
First Name & Middle Initial & Last Name & Degree
Daniella Soba, OTD
Phone
718-839-7104
Email
dsoba@montefiore.org

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Publication in high impact autism journal, and presentation at international autism research meetings.
IPD Sharing Time Frame
Data will be available following completion of the study and publication of findings.
IPD Sharing Access Criteria
Upon written request (reviewed by principal investigator) information will be shared.

Learn more about this trial

Telehealth Intervention for Autism Spectrum Disorder

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