search
Back to results

Refinements of Functional Communication Training

Primary Purpose

Aggression, Self-injurious Behavior

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Trad FCT
Mult FCT
Mult FCT + Stimulus Fading
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aggression

Eligibility Criteria

3 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Boys and girls from ages 3 to 17
  • Destructive behavior that occurs at least 10 times a day despite previous treatment
  • Destructive behavior reinforced by social consequences like attention (FCT is not appropriate for automatically reinforced destructive behavior)
  • On a stable psychoactive drug regimen for at least 10 half-lives per drug or drug free
  • Stable educational plan and placement with no anticipated changes during the child's treatment

Exclusion Criteria:

  • Patients who do not meet the inclusion criteria
  • Patients currently receiving 15 or more hours per week of treatment for their destructive behavior
  • DSM-5 diagnosis of Rett syndrome or other degenerative conditions (e.g., inborn error of metabolism)
  • A comorbid health condition or major mental disorder that would interfere with study participation
  • Occurrence of SIB during study assessments that presents a risk of serious or permanent harm (e.g., detached retinas) based on our routine clinical-risk assessment
  • Patients requiring drug-treatment changes, but the experimenters will invite these patients to participate if they meet inclusion criteria after drug regimen is stable.

Sites / Locations

  • Children's Specialized Hospital - Rutgers University Center for Autism Research, Education, and ServicesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Mult FCT/Trad FCT

Mult FCT + Stimulus Fading/Trad FCT

Arm Description

Participants assigned to this condition will receive both traditional FCT (trad FCT) and FCT with multiple schedules (mult FCT) to evaluate the effects of mult FCT on renewal, super-resurgence, and reinstatement.

Participants assigned to this condition will receive both traditional FCT (trad FCT) and FCT with multiple schedules and stimulus fading (mult FCT + stimulus fading) to evaluate the effects of mult FCT and gradual fading of contextual stimuli on renewal, super-resurgence, and reinstatement.

Outcomes

Primary Outcome Measures

Rate of Destructive Behavior in Renewal Test
The investigators will measure the rate of destructive behavior following successful treatment when the FCT is implemented in a context not associated with treatment (e.g., the baseline, home-like context).
Rate of Destructive Behavior in Super-Resurgence Test
The investigators will measure the rate of destructive behavior when FCT is implemented in a context not associated with treatment (e.g., a classroom context) by an implementer who fails to reinforce the communication response. This would be similar to a busy teacher in a classroom who is unable to attend to the child due to assisting another student.
Rate of Destructive Behavior in Reinstatement Test
The investigators will measure the rate of destructive behavior when FCT is not implemented as prescribed (i.e., reinforcement is delivered on a time-based schedule, rather than following communication responses). This would be similar to a teacher who delivers breaks from work based on the school schedule (e.g., switching from math to reading) rather than the child's request for a break during the math period).

Secondary Outcome Measures

Full Information

First Posted
August 1, 2019
Last Updated
May 15, 2023
Sponsor
Rutgers, The State University of New Jersey
search

1. Study Identification

Unique Protocol Identification Number
NCT04045600
Brief Title
Refinements of Functional Communication Training
Official Title
Stimulus Control Refinements of Functional Communication Training
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 3, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey

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
Although treatments for problem behavior, like functional communication training (FCT), can be highly effective in the clinic, changes in the way the FCT is implemented (e.g., when transferring treatment to the home, when teachers implement treatment with poor fidelity) can result in treatment relapse. The goal of this study is to evaluate whether using treatment signals and gradually introducing materials from natural contexts can help mitigate treatment relapse during context changes and poor treatment-integrity scenarios.
Detailed Description
The most common treatment for problem behavior is functional communication training (FCT). FCT involves teaching children to request what they want, rather than engaging in problem behavior when they don't get their way, and then teach them that they cannot always ask for their way and instead must wait or work appropriately first. While FCT is effective, problem behavior sometimes comes back after treatment when children encounter treatment challenges, like long periods of not getting their way, when caregivers deliver treatment differently than what they are used to (e.g., caregivers delivering FCT incorrectly), or experiencing treatment in a new place (e.g., the home, the classroom). The purpose of this research study is to determine whether the experimenters can reduce the chances of children returning to problem behavior during these challenges by teaching them to pay attention to treatment signals (e.g., a red card that indicates treatment is in place) and gradually changing the treatment setting to appear more like the home or classroom. First, the experimenters will provide each child with their way in a home-like environment containing a couch, rug, etc. Next, within a barren therapy room, the experimenters will conduct two of the following three types of treatments: (1) a treatment with no signals that indicate when their child can and cannot have their way, (2) a treatment with signals, and (3) a treatment with signals plus introduction of items from the natural environment such as rugs and couches. Then, the experimenters will introduce three common treatment challenges in a row to determine whether treatment signals reduce relapse of problem behavior. First, the experimenters will introduce the treatments in the home-like environment to see if the child continues to respond appropriately in a setting different than the therapy room. Second, the experimenters will simulate a transition to the school by having the child experience treatment in a classroom-like environment (e.g., with desks and chalkboards) while the teacher makes the child wait a long period of time to get their way. This would be similar to when a teacher cannot give the child attention or a preferred item because they are busy with other students. Third, the experimenters will simulate the teacher implementing treatment differently than the child is used to in the classroom by the teacher delivering preferred activities according to a timed schedule rather than when the child asks. This simulates the common event of a teacher delivering preferred activities like breaks or recess regardless of the child's behavior. The goal is to determine how well the treatments perform across each of these common challenges.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aggression, Self-injurious Behavior

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mult FCT/Trad FCT
Arm Type
Experimental
Arm Description
Participants assigned to this condition will receive both traditional FCT (trad FCT) and FCT with multiple schedules (mult FCT) to evaluate the effects of mult FCT on renewal, super-resurgence, and reinstatement.
Arm Title
Mult FCT + Stimulus Fading/Trad FCT
Arm Type
Experimental
Arm Description
Participants assigned to this condition will receive both traditional FCT (trad FCT) and FCT with multiple schedules and stimulus fading (mult FCT + stimulus fading) to evaluate the effects of mult FCT and gradual fading of contextual stimuli on renewal, super-resurgence, and reinstatement.
Intervention Type
Behavioral
Intervention Name(s)
Trad FCT
Intervention Description
This intervention emulates a traditional reinforcement schedule-thinning method during FCT in which clinicians program delays to reinforcement without discriminative stimuli (e.g., the child learns that some FCRs result in reinforcement and some do not). By programming reinforcement approximately every 15 s, the rate of reinforcement will be equivalent to mult FCT. During Period 1 of this project, trad FCT served as an appropriate control condition to which mult FCT could be compared.
Intervention Type
Behavioral
Intervention Name(s)
Mult FCT
Intervention Description
This intervention involves correlating discriminative stimuli (e.g., purple and yellow index cards) with times in which reinforcement for the functional communication response (FCR) is and is not available. During Period 1 of this project, this procedure resulted in rapid reduction of destructive behavior and mitigated resurgence and renewal when the discriminative stimuli were used as programmed.
Intervention Type
Behavioral
Intervention Name(s)
Mult FCT + Stimulus Fading
Intervention Description
This condition is similar to mult FCT except that the experimenters will gradually incorporate natural stimuli (e.g., rugs, tables, lamps) into sessions to approximate target settings that may occasion relapse typically without such gradual stimulus fading.
Primary Outcome Measure Information:
Title
Rate of Destructive Behavior in Renewal Test
Description
The investigators will measure the rate of destructive behavior following successful treatment when the FCT is implemented in a context not associated with treatment (e.g., the baseline, home-like context).
Time Frame
Through study completion, an average of 3 weeks.
Title
Rate of Destructive Behavior in Super-Resurgence Test
Description
The investigators will measure the rate of destructive behavior when FCT is implemented in a context not associated with treatment (e.g., a classroom context) by an implementer who fails to reinforce the communication response. This would be similar to a busy teacher in a classroom who is unable to attend to the child due to assisting another student.
Time Frame
Through study completion, an average of 3 weeks.
Title
Rate of Destructive Behavior in Reinstatement Test
Description
The investigators will measure the rate of destructive behavior when FCT is not implemented as prescribed (i.e., reinforcement is delivered on a time-based schedule, rather than following communication responses). This would be similar to a teacher who delivers breaks from work based on the school schedule (e.g., switching from math to reading) rather than the child's request for a break during the math period).
Time Frame
Through study completion, an average of 3 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Boys and girls from ages 3 to 17 Destructive behavior that occurs at least 10 times a day despite previous treatment Destructive behavior reinforced by social consequences like attention (FCT is not appropriate for automatically reinforced destructive behavior) On a stable psychoactive drug regimen for at least 10 half-lives per drug or drug free Stable educational plan and placement with no anticipated changes during the child's treatment Exclusion Criteria: Patients who do not meet the inclusion criteria Patients currently receiving 15 or more hours per week of treatment for their destructive behavior DSM-5 diagnosis of Rett syndrome or other degenerative conditions (e.g., inborn error of metabolism) A comorbid health condition or major mental disorder that would interfere with study participation Occurrence of SIB during study assessments that presents a risk of serious or permanent harm (e.g., detached retinas) based on our routine clinical-risk assessment Patients requiring drug-treatment changes, but the experimenters will invite these patients to participate if they meet inclusion criteria after drug regimen is stable.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wayne W Fisher, PhD
Phone
8488008503
Email
wayne.fisher@rutgers.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Serena Claiborne
Phone
8488008504
Email
SClaiborne@childrens-specialized.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wayne W Fisher, PhD
Organizational Affiliation
Rutgers, The State University of New Jersey
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Specialized Hospital - Rutgers University Center for Autism Research, Education, and Services
City
Somerset
State/Province
New Jersey
ZIP/Postal Code
00873
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wayne Fisher, PhD
Phone
848-800-8503
Email
wayne.fisher@rutgers.edu
First Name & Middle Initial & Last Name & Degree
Serena Claiborne
Phone
8488008504
Email
sclaiborne@childrens-specialized.org

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The experimenters plan to make data available to participants, if requested, and submit results for publication.
IPD Sharing Time Frame
The informed consent form shall be available to the caregiver immediately after caregiver signature. If requested, the study protocol will be sent to the caregiver after the study is complete.
IPD Sharing Access Criteria
Each caregiver of a child enrolled in the study will be eligible to receive the above documents.

Learn more about this trial

Refinements of Functional Communication Training

We'll reach out to this number within 24 hrs