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Project AFECT (Autism Family Empowerment Coaching and Training Program) (AFECT)

Primary Purpose

Autism Spectrum Disorder, Autism, Autism Spectrum Disorders

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Autism Family Empowerment Coaching and Training Program
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Autism Spectrum Disorder focused on measuring Parent Coaching, Family Navigation, Parent Training, Parent Stress, Parent Self-Efficacy, Service Navigation

Eligibility Criteria

12 Months - 60 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 1. Parents of children just diagnosed with autism (with or without other diagnoses) who are: Age greater than 1 and up to 5 years old; Hispanic/Latino OR Black/African-American OR have Medi-Cal as primary health insurance; AND Live in one of the following counties in California (Alameda, Contra Costa, Marin, Monterey, Napa, San Benito, San Francisco, San Mateo, Santa Clara, Santa Cruz, Solano, or Sonoma). Exclusion Criteria: Non-legal guardians or foster parents who provide care to children newly diagnosed with autism. Parents of children without diagnosis of autism.

Sites / Locations

  • Gardner Packard Children's Health CenterRecruiting
  • Stanford Medicine Children's HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Treatment As Usual Group

Coaching Group

Arm Description

This group will receive treatment as usual.

Coaching Group will receive Project AFECT intervention, in addition to treatment as usual.

Outcomes

Primary Outcome Measures

Self-Efficacy
Mean change from baseline in parental self-efficacy measured using Autism-Specific Parenting Self-Efficacy Scale (PSEaS). Overall possible scores on the scale range from 17 - 85. The higher the score, the higher the measured level of parental self-efficacy (better outcome).
Stress Level
Mean change from baseline in parental stress level measured using Parental Stress Scale (PSS). Overall possible scores on the scale range from 18 - 90. The higher the score, the higher the measured level of parental stress (worse outcome).

Secondary Outcome Measures

Child's Language Development
Scores using MacArthur-Bates Communicative Development Inventory - Words and Gestures. For comparison between groups, we will be utilizing the raw scores. Overall possible raw scores range from 0 - 396. The higher the raw score, the higher the number of words understood and produced by the child (better outcome).
Wait time to autism treatments
Time from initial autism diagnosis to start of applied behavior analysis (ABA) therapy
Wait time to early intervention/special education
Time from initial autism diagnosis to assessment for early intervention/special education and development of Individualized Family Service Plan (IFSP)/Individualized Education Program (IEP)

Full Information

First Posted
June 9, 2023
Last Updated
October 13, 2023
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT05910502
Brief Title
Project AFECT (Autism Family Empowerment Coaching and Training Program)
Acronym
AFECT
Official Title
Autism Family Empowerment Coaching and Training Program (AFECT): Evaluating a Parent Coaching and Family Navigation Program for New Autism Spectrum Disorder Diagnosis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 19, 2023 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University

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
The goal of this clinical trial is to learn about the journey of families after their child's diagnosis of autism and to help parents understand autism and get the right treatments for their child. This study is for parents of children just diagnosed with autism who are: Age greater than 1 and up to 5 years old; Hispanic/Latino OR Black/African-American OR have Medi-Cal as primary health insurance; AND Live in one of the following counties in California (Alameda, Contra Costa, Marin, Monterey, Napa, San Benito, San Francisco, San Mateo, Santa Clara, Santa Cruz, Solano, or Sonoma). The main questions it aims to answer are: Whether parent coaching through Project AFECT leads to decreased parental stress and increased parental confidence; Whether family navigation through Project AFECT leads to increased number of referrals to early intervention and educational services and reduced wait times to autism treatments; Whether children whose parents receive Project AFECT intervention show increased language skills compared to children whose parents did not receive intervention. Participants will be asked to: Complete surveys at enrollment and 3 and 6 months later. Work with Project AFECT Coach. Researchers will compare control and intervention groups to see if Project AFECT leads to improved parent and child outcomes.
Detailed Description
This is a prospective clinical effectiveness study of Project AFECT, an intervention combining parent coaching and family navigation. Parents who meet inclusion criteria will be invited to participate in this study at the time of their child's autism diagnosis at Stanford Medicine Children's Health. Participants in the control group will receive treatment as usual. In addition to treatment as usual, participants in the intervention group will be connected with Project AFECT Coaches who will provide: Coaching to (1) assure parents understand diagnosis, (2) assist parents in finding accurate, current information about autism, (3) guide parents to free online autism training resources, (4) empower parents to evaluate child's intervention plan holistically, and (5) provide emotional support to reduce stress; Navigation to (1) help family access autism treatments, and (2) connect to early intervention and educational services.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder, Autism, Autism Spectrum Disorders, Autistic Disorder, Autistic Spectrum Disorder, Autistic Spectrum Disorders, Autistic Disorders Spectrum
Keywords
Parent Coaching, Family Navigation, Parent Training, Parent Stress, Parent Self-Efficacy, Service Navigation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Waitlist control Participants in the control group will be offered the opportunity to participate in the intervention group if the child has not received any autism treatments 6 months after enrollment in this study.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment As Usual Group
Arm Type
No Intervention
Arm Description
This group will receive treatment as usual.
Arm Title
Coaching Group
Arm Type
Experimental
Arm Description
Coaching Group will receive Project AFECT intervention, in addition to treatment as usual.
Intervention Type
Behavioral
Intervention Name(s)
Autism Family Empowerment Coaching and Training Program
Other Intervention Name(s)
Project AFECT
Intervention Description
Participants in the intervention group will be connected with Project AFECT Coaches who will provide: Coaching to (1) assure parents understand diagnosis, (2) assist parents in finding accurate, current information about autism, (3) guide parents to free online autism training resources, (4) empower parents to evaluate child's intervention plan holistically, and (5) provide emotional support to reduce stress; Navigation to (1) help family access autism treatments, and (2) connect to early intervention and educational services.
Primary Outcome Measure Information:
Title
Self-Efficacy
Description
Mean change from baseline in parental self-efficacy measured using Autism-Specific Parenting Self-Efficacy Scale (PSEaS). Overall possible scores on the scale range from 17 - 85. The higher the score, the higher the measured level of parental self-efficacy (better outcome).
Time Frame
From enrollment to the end of intervention at 6 months
Title
Stress Level
Description
Mean change from baseline in parental stress level measured using Parental Stress Scale (PSS). Overall possible scores on the scale range from 18 - 90. The higher the score, the higher the measured level of parental stress (worse outcome).
Time Frame
From enrollment to the end of intervention at 6 months
Secondary Outcome Measure Information:
Title
Child's Language Development
Description
Scores using MacArthur-Bates Communicative Development Inventory - Words and Gestures. For comparison between groups, we will be utilizing the raw scores. Overall possible raw scores range from 0 - 396. The higher the raw score, the higher the number of words understood and produced by the child (better outcome).
Time Frame
From enrollment to the end of intervention at 6 months
Title
Wait time to autism treatments
Description
Time from initial autism diagnosis to start of applied behavior analysis (ABA) therapy
Time Frame
From enrollment to the end of intervention at 6 months
Title
Wait time to early intervention/special education
Description
Time from initial autism diagnosis to assessment for early intervention/special education and development of Individualized Family Service Plan (IFSP)/Individualized Education Program (IEP)
Time Frame
From enrollment to the end of intervention at 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
60 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Parents of children just diagnosed with autism (with or without other diagnoses) who are: Age greater than 1 and up to 5 years old; Hispanic/Latino OR Black/African-American OR have Medi-Cal as primary health insurance; AND Live in one of the following counties in California (Alameda, Contra Costa, Marin, Monterey, Napa, San Benito, San Francisco, San Mateo, Santa Clara, Santa Cruz, Solano, or Sonoma). Exclusion Criteria: Non-legal guardians or foster parents who provide care to children newly diagnosed with autism. Parents of children without diagnosis of autism.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ingrid Lin, MD
Phone
650-725-0555
Email
ingridyl@stanford.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heidi Feldman, MD, PhD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gardner Packard Children's Health Center
City
Atherton
State/Province
California
ZIP/Postal Code
94027
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ingrid Lin, MD
Phone
650-725-0555
Email
ingridyl@stanford.edu
First Name & Middle Initial & Last Name & Degree
Heidi Feldman, MD, PhD
Facility Name
Stanford Medicine Children's Health
City
Sunnyvale
State/Province
California
ZIP/Postal Code
94087
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ingrid Lin, MD
Phone
650-725-0555
Email
ingridyl@stanford.edu
First Name & Middle Initial & Last Name & Degree
Heidi Feldman, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After conclusion of this study and publication of the main findings, de-identified data will be placed in a public repository.
IPD Sharing Time Frame
June 30, 2026 to June 30, 2031
IPD Sharing Access Criteria
To be determined

Learn more about this trial

Project AFECT (Autism Family Empowerment Coaching and Training Program)

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