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Manualized Assessment and Treatment Model of Challenging Behavior

Primary Purpose

Problem Behavior, Aggression, Self-Injury

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Functional Communication Training (FCT)
Non-Contingent Reinforcement (NCR)
Competing Items and Response Blocking
Research Units in Behavioral Intervention (RUBI) protocol
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 Problem Behavior

Eligibility Criteria

3 Years - 17 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: children from ages 3 to 17; challenging behavior that occurs at least 10 times a day, despite previous treatment; challenging behavior maintained by social positive or automatic reinforcement; stable protective supports for self-injurious behavior (e.g., helmet) with no anticipated changes during enrollment; 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 challenging 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 self-injury during study assessments that presents a risk of serious or permanent harm (e.g., detached retinas) based on our routine clinical-risk assessment (Betz, 2011); patients requiring changes to protective supports for self-injury or drug treatment, but we will invite these patients to participate when protective supports and drug regimen are stable.

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Functional Analysis Treatment for Harmful Challenging Behavior

Functional Analysis Treatment for Milder Challenging Behavior

Arm Description

If challenging behavior is found to be socially maintained, we will recommend functional communication training (FCT) to teach a functional communication response (FCR) (e.g., touching a card with a picture of the participant consuming the reinforcer), but we will also offer NCR as a potential treatment option to the caregivers. During FCT, reinforcement will be discontinued for challenging behavior and only the alternative communication response will be reinforced. If the parents choose NCR over FCT for socially maintained challenging behavior, we will deliver the functional and competing reinforcers on time-based schedules. If challenging behavior is found to be automatically maintained, we will recommend using NCR with competing items and response blocking for treatment. We will use multiple and chained schedules to thin the reinforcement schedules and increase the practicality of these treatments.

Caregivers of patients with mild challenging behavior will receive training using the Research Units in Behavioral Intervention (RUBI) protocol informed by the functional analysis conducted as a part of the initial assessment (Bearss et al., 2018). The RUBI protocol includes 11 core modules and 7 optional modules on training caregivers to apply behavior-analytic techniques to help manage challenging behaviors.

Outcomes

Primary Outcome Measures

Rate of Problem Behavior
The investigators will collect continuous, direct-observation measures of destructive behavior throughout all phases of the study. They will compare rates of destructive behavior during assessment, treatment, caregiver training, and followup.

Secondary Outcome Measures

Caregiver report
The investigators will compare caregiver reports of targeted problem behavior severity during treatment across the two experimental groups.
Clinical Global Impressions Severity Subscale
The investigators will compare the severity of targeted topographies of problem behavior during treatment across the two experimental groups using the Clinical Global Impressions Severity Subscale. Severity is rated on a seven-point scale, ranging from 1 (normal) to 7 (among the most severe).
Aberrant Behavior Checklist Irritability Subscale
The investigators will compare the generalized effects of treatment on both targeted and non-targeted problem behavior across both experimental groups using the Aberrant Behavior Checklist irritability Subscale. The irritability subscale contains 15 items. Irritability items are scored using a four-point scale, ranging from 0 (not at all a problem) to 3 (the problem is severe in degree). A higher composite score of all irritability items indicates greater severity.

Full Information

First Posted
June 15, 2023
Last Updated
June 28, 2023
Sponsor
Rutgers, The State University of New Jersey
Collaborators
Autism Speaks
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1. Study Identification

Unique Protocol Identification Number
NCT05928247
Brief Title
Manualized Assessment and Treatment Model of Challenging Behavior
Official Title
Manualized Assessment and Treatment Model of Challenging Behavior
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 2023 (Anticipated)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

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

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
Despite decades of mounting single-case-design evidence for the efficacy of applied behavior analysis (ABA) and other approaches for the assessment and treatment of challenging behavior, an evidence-based comprehensive approach remains to exist. The current study will collect test the efficacy of a standardized manual for assessing and treating challenging behavior for individuals with severe and mild challenging behavior.
Detailed Description
The investigators will stratify participants according to the severity of their challenging behavior (harmful or milder forms of challenging behavior). Criteria for Harmful Challenging Behavior Participants will be classified as exhibiting harmful challenging behavior if they meet all the following criteria and as exhibiting milder challenging behavior if they do not meet all these criteria. The child displays one or more of the following challenging behaviors (operationally defined on the Destructive Behavior Severity Scale, see attached) daily: (a) aggression, (b) elopement, (c) injury risk behavior, (d) pica, (e) property destruction, and/or (f) SIB. The child's challenging behaviors are at a severity level that poses a clear and serious risk to oneself, others, or the environment (Severity Level 2 or higher on the Destructive Behavior Severity Scale, see attached). The child's challenging behavior causes clear and significant stress on the child's family members (e.g., siblings are deprived of parental attention; family members are restricted from maintaining employment, going on family outings, attending church, eating at a restaurant, or taking a vacation due to the child's challenging behavior). The child has had at least 3 months of outpatient behavior therapy with insufficient improvement in the challenging behavior or the child's challenging behavior poses an imminent danger to oneself or others such that less intensive services would be contraindicated. The child has had at least 3 months of outpatient psychopharmacological intervention by a psychiatrist or developmental pediatrician with insufficient improvement in the challenging behavior, or the psychiatrist or developmental pediatrician has recommended adding intensive behavioral intervention. The manualized protocol has three general components that will be used with participants in both groups including: (a) assessment, (b) treatment, and (c) caregiver training and generalization. Assessment Trial-Based Functional Analysis (FA) The investigators will begin by conducting a trial-based FA with each participant. During the trial-based FA, a multielement design will be used to evaluate conditions that maintain challenging behavior. During the first series of conditions, researchers will measure the latency to engage in challenging behavior from the start of each trial to determine an appropriate duration subsequent for trials. Conditions will be evaluated in the following order: monitored ignore/alone, attention, toy-play, escape, and tangible. Other conditions (e.g., social avoidance) will be evaluated as appropriate for each participant if little or no challenging behavior is observed in above conditions. Researchers will wear colored shirts to signal each condition. After the first series of trials (i.e., one trial per condition), the duration of each subsequent trial will be determined by multiplying the latency for each condition by 1.5. The minimum trial duration will be 30 s and the maximum trial duration will be 5 min. Each condition will arrange specific antecedent and consequent conditions for challenging behavior. Specifically, evocative events will be arranged (e.g., restricting attention in the attention condition) and contingent on the first instance of challenging behavior, reinforcement will be delivered for 20 s (e.g., attention will be delivered in the attention condition). Rates of challenging behavior will be analyzed across conditions to determine the variable(s) that maintained challenging behavior. Multielement FA If definitive conclusions cannot be drawn about the conditions that maintain challenging behavior from the trial-based FA, the investigators will conduct a more-extended and traditional multielement FA. The multielement FA will begin with a 15 min monitored ignore screener to rule in or rule out automatic maintenance of challenging behavior (maintained by conditions other than those that researchers have control over). During this session, researchers will not provide any consequences for challenging behavior. Following the initial monitored ignore session, researchers will evaluate social conditions that maintain challenging behavior in a multielement design. All social test sessions will last 5 min. Conditions will be evaluated in the following order: monitored ignore/alone, attention, toy-play, escape, and tangible. Other conditions will be evaluated as appropriate for each participant (e.g., social avoidance). Researchers will wear colored shirts to signal each condition. Monitored ignore conditions will be conducted like the initial screener. During the social test conditions (attention, tangible, and escape), researchers will systematically arrange evocative conditions and deliver consequences contingent on challenging behavior. For example, during the escape condition, researchers will begin the session by delivering instructions to complete tasks. Researchers will deliver brief praise for task completion. Contingent on challenging behavior, researchers will provide a break from tasks for 20 s to determine whether escape from nonpreferred tasks maintains challenging behavior. Following 20 s, researchers will begin delivering instructions again until the next instance of challenging behavior. This sequence of events will continue until 5 min have elapsed. The toy-play condition will serve as the control condition, in which participants will have access to highly preferred tangible items and attention, and no task instructions will be delivered. The investigators will conduct a minimum of five sessions per conditions (e.g., five attention sessions). Rates of challenging behavior will be analyzed across conditions to determine the variables maintaining challenging behavior. Treatment Treatment decisions will be driven by informed caregiver preferences and choices. That is, the investigators will use the results of our assessments to inform caregivers regarding all the treatment options and choices available to them. For example, if two or more behavioral treatments (e.g., functional communication training or noncontingent reinforcement) are reasonable options for the patient, the supervising behavior analyst will explain the potential benefits and risks associated with each option and ask the caregiver to choose between them. Harmful Challenging Behavior Once the variable(s) that maintain challenging behavior are identified, the investigators will inform caregivers of the treatment options and develop a function-based treatment for each participant. If challenging behavior is found to be socially maintained, the investigators will typically recommend functional communication training (FCT) to teach a functional communication response (FCR) (e.g., touching a card with a picture of the participant consuming the reinforcer), but the investigators will also offer NCR as a potential treatment option to the caregivers. During FCT, reinforcement will be discontinued for challenging behavior and only the alternative communication response will be reinforced. For participants with challenging behavior determined to be maintained by social-positive reinforcement (attention and/or tangible), the investigators also will typically recommend using a multiple schedule FCT (mult-FCT) to signal when reinforcement is available and to thin the schedule of reinforcement to render the treatment more practical for caregivers to implement. For participants with challenging behavior determined to be maintained by social-negative reinforcement (escape), the investigators will recommend using a chained schedule FCT (chained-FCT). If the parents choose NCR over FCT for socially maintained challenging behavior, the investigators will deliver the functional and competing reinforcers on time-based schedules and use multiple and chained schedules to signal when noncontingent reinforcement is available (similar to multiple- and chained-FCT). If challenging behavior is found to be automatically maintained, the investigators will recommend using NCR with competing items and response blocking for treatment. The investigators will also use multiple and chained schedules to thin the reinforcement schedules and increase the practicality of the this treatment. Functional Communication Training Pretraining. The investigators will train participants to use the FCR during mult-FCT and chained-FCT using prompting and prompt fading. Mult-FCT. The investigators will choose two colored signals and randomly assign two different colored cards as the SD (which signals the availability of reinforcement) and S-delta (which signals the unavailability of reinforcement). The session will start with an SD component followed by an S-delta component followed by a quasi-random rotation of the SD and S-delta components. SD and S-delta components will be 60 s and 2 s, respectively. If the participant uses the FCR without displaying challenging behavior for at least 3 s during the SD component, the therapist will deliver functional reinforcement for the rest of the SD component. If the participant emits a challenging behavior within 3 s of emitting the FCR, the therapist will withhold reinforcement until the participant emits FCR without also emitting challenging behavior. The therapist will deliver no differential consequence (extinction) for the FCR with the S-delta present and for challenging behavior during the SD and S-delta components (extinction). The duration of the S-delta component will be systematically increased as challenging behavior remains low and independent FCRs remain high to make the treatment more practical for caregivers. Chained-FCT. The procedures for chained-FCT will be like mult-FCT, except participants will be required to complete work (e.g., academics, daily living skills) during the S-delta component. The SD component will be 20 s and the S-delta component will be as long as it takes participants to complete one task. Initially, the participant will be required to complete just one task (e.g., fold one towel) during the S-delta component. Over time, the number of tasks required during the S-delta component will be systematically increased as challenging behavior remains low, task completion remains high, and independent FCRs remain high. Competing Items and Response Blocking. We will conduct a competing stimulus assessment (CSA) to identify items that produce at least an 80% reduction in challenging behavior when the participant is engaged with them. The investigators will evaluate conditions in which participants have free access to the item(s), when engagement with the item(s) is prompted, and when challenging behavior is physically blocked. Treatment will include one or more of the following components: non-contingent reinforcement informed by the CSA, reinforcing adaptive behavior, and blocking challenging behavior. The ending duration of the S-delta component will be based on input from caregivers and the participant's school personnel. Mild Challenging Behavior Once the variable(s) that maintain challenging behavior are identified, the investigators will inform caregivers of the treatment options and develop a function-based treatment for each participant. Caregivers of patients with mild challenging behavior will receive training using the Research Units in Behavioral Intervention (RUBI) protocol informed by the functional analysis conducted as a part of the initial assessment (Bearss et al., 2018). The results of the functional analysis will inform the development of the training delivered as part of the RUBI protocol. An outline of the standard RUBI protocol is displayed below. Week 1: Introduction to behavioral principles Week 2: Prevention strategies Week 3: Daily schedules Week 4: Home visit and assessment Weel 5: Reinforcement I Week 6: Reinforcement II Week 7: Planned ignoring Week 8: Assessment Week 9: Compliance training Week 10: Functional communication training Week 11: Teaching skills I Week 12: Assessment Week 13: Teaching skills II Week 14: Generalization & maintenance Week 15: Optional lessons Week 16: Assessment Week 18: Telephone booster Caregiver training and generalization Using a combination of training strategies (e.g., behavioral skills training, video modeling) and caregiver preference, the investigators will train participants' caregivers to implement treatment techniques with accuracy. The investigators will generalize treatment effects for all patients to novel people and settings and maintain an 80% reduction in challenging behavior and high levels (85% or higher) of appropriate behavior (e.g., FCRs). Harmful Challenging Behavior. The investigators will train at least one of the caregivers to 90% or greater accuracy when implementing the techniques below. To maximize safety, the investigators will assess caregiver behavior with therapists role-playing as the patient before the investigators have the caregiver implement the skills with the patient directly. Caregiver training will include the steps listed and described below, and the investigators anticipate progressing to a new step each week of the patient's admission in the Severe Behavior Program: We will collaborate with the caregiver to identify critical safety concerns within the home or community and teach strategies to minimize risk (e.g., clearing rooms during challenging behavior, using buckle guards to reduce out-of-seat behavior during transportation). We will train the caregiver in the following behavior-management techniques until the caregiver responds with 90% or greater accuracy for each of the following: Responses to aggression role played by behavior analyst, Responses to self-injurious behavior role played by behavior analyst, Procedures for managing challenging behavior that poses imminent threat with a behavior analyst role-playing as the patient We will teach the caregiver to identify the common functions of challenging behavior. The caregiver will respond with 90% accuracy to comprehension questions. We will teach the caregiver how to collect data at home relevant to the patient's challenging and adaptive behavior. The caregiver will display 90% or greater data accuracy when the behavior analysts role plays as the patient with challenging behavior. We will teach the caregiver about extinction and train the caregiver to implement extinction procedures relevant to the patient's initial treatment arrangement. The caregiver will display 90% or greater accuracy when the behavior analyst role plays as the patient with challenging behavior. We will teach the caregiver about reinforcement-based interventions and train the caregiver to deliver differential reinforcement of alternative or other behavior and noncontingent reinforcement relevant to the patient's initial treatment arrangement. The caregiver will display 90% or greater accuracy when the behavior analyst role plays as the patient with challenging behavior. We will train the caregiver to implement three-step guided compliance procedures. The caregiver will display 90% or greater accuracy when the behavior analyst role plays as the patient with challenging behavior. We will teach the caregiver about the importance of conducting periodic preference assessments with the participant and how to implement one practically. The caregiver will display 90% or greater accuracy when the behavior analyst role plays as a patient during a preference assessment. We will train the caregiver to implement the reinforcement component of the patient's terminal treatment package. The caregiver will display 90% or greater accuracy (a) when the behavior analyst role plays as the patient with challenging behavior and (b) during two sessions with the patient. We will train the caregiver to implement the extinction component of the patient's terminal treatment package. The caregiver will display 90% or greater accuracy (a) when the behavior analyst role plays as the patient with challenging behavior and (b) during two sessions with the patient. We will train the caregiver to implement both the reinforcement and extinction components of the patient's terminal treatment package while also managing challenging behavior. The caregiver will display 90% or greater accuracy (a) when the behavior analyst role plays as the patient with challenging behavior and (b) during two sessions with the patient. We will coach the caregiver to conduct the entirety of the patient's treatment at the terminal schedule with minimal trainer involvement. The caregiver will display 90% or greater accuracy during two sessions with the patient without requiring therapist feedback. Milder Challenging Behavior. Caregivers of patients with mild challenging behavior will receive training on a variety of topics throughout implementation of the RUBI protocol (outlined above). Data Points For participants with harmful challenging behavior who are being treated in our intensive outpatient clinic, trained observers will use laptop computers with BDataPro® software developed in our lab to score frequency of participant challenging behavior and therapist behavior. The investigators will define challenging behavior as pushing, pinching, scratching, kicking, or biting others; hitting others with body parts or objects; banging, throwing, overturning, or tearing objects; climbing on objects not made for that purpose; striking, scratching, rubbing, poking, or biting self. The investigators will convert challenging-behavior frequency to a rate by dividing the number of responses in a session by the session duration in minutes. The investigators will assess procedural integrity by scoring whether therapists correctly implemented the planned antecedents, prompts, and consequences for target responses. The investigators will convert correct antecedents, prompts, and consequences to a percentage after dividing the number of correct responses by the number of correct-response opportunities. Observation, reliability, and validity of dependent and procedural-integrity measures. A second observer will score at least 1/3 of sessions independently to assess data accuracy (reliability). Observers will score procedural integrity for at least 1/3 of sessions. The investigators will retrain therapists with less than 90% procedural integrity for two consecutive sessions. For patients with mild challenging behavior who are receiving the RUBI program, the investigators will collect indirect measures of challenging behavior via caregiver report during each week of training. Additionally, the investigators will use the Destructive Behavior Severity Scale, the Clinical Global Impressions Severity Subscale, and the Aberrant Behavior Checklist-Irritability Subscale to collect data on challenging behavior. These assessments will be administered at each week labeled as "Assessment" in the above outline for the RUBI program

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Functional Analysis Treatment for Harmful Challenging Behavior
Arm Type
Experimental
Arm Description
If challenging behavior is found to be socially maintained, we will recommend functional communication training (FCT) to teach a functional communication response (FCR) (e.g., touching a card with a picture of the participant consuming the reinforcer), but we will also offer NCR as a potential treatment option to the caregivers. During FCT, reinforcement will be discontinued for challenging behavior and only the alternative communication response will be reinforced. If the parents choose NCR over FCT for socially maintained challenging behavior, we will deliver the functional and competing reinforcers on time-based schedules. If challenging behavior is found to be automatically maintained, we will recommend using NCR with competing items and response blocking for treatment. We will use multiple and chained schedules to thin the reinforcement schedules and increase the practicality of these treatments.
Arm Title
Functional Analysis Treatment for Milder Challenging Behavior
Arm Type
Experimental
Arm Description
Caregivers of patients with mild challenging behavior will receive training using the Research Units in Behavioral Intervention (RUBI) protocol informed by the functional analysis conducted as a part of the initial assessment (Bearss et al., 2018). The RUBI protocol includes 11 core modules and 7 optional modules on training caregivers to apply behavior-analytic techniques to help manage challenging behaviors.
Intervention Type
Behavioral
Intervention Name(s)
Functional Communication Training (FCT)
Intervention Description
During FCT, reinforcement will be discontinued for challenging behavior and only the alternative communication response will be reinforced. For participants with challenging behavior determined to be maintained by social-positive reinforcement (attention and/or tangible), we also will typically recommend using a multiple schedule FCT (mult-FCT) to signal when reinforcement is available and to thin the schedule of reinforcement to render the treatment more practical for caregivers to implement. For participants with challenging behavior determined to be maintained by social-negative reinforcement (escape), we will recommend using a chained schedule FCT (chained-FCT).
Intervention Type
Behavioral
Intervention Name(s)
Non-Contingent Reinforcement (NCR)
Intervention Description
During NCR, we will deliver the functional and competing reinforcers on time-based schedules and use multiple and chained schedules to signal when noncontingent reinforcement is available (similar to multiple- and chained-FCT).
Intervention Type
Behavioral
Intervention Name(s)
Competing Items and Response Blocking
Intervention Description
We will conduct a competing stimulus assessment (CSA) to identify items that produce at least an 80% reduction in challenging behavior when the participant is engaged with them. We will evaluate conditions in which participants have free access to the item(s), when engagement with the item(s) is prompted, and when challenging behavior is physically blocked. Treatment will include one or more of the following components: non-contingent reinforcement informed by the CSA, reinforcing adaptive behavior, and blocking challenging behavior. We will also use multiple and chained schedules to thin the reinforcement schedules and increase the practicality of the this treatment. The ending duration of the S-delta component will be based on input from caregivers and the participant's school personnel.
Intervention Type
Behavioral
Intervention Name(s)
Research Units in Behavioral Intervention (RUBI) protocol
Intervention Description
Caregivers of participants with mild challenging behavior will receive training on a variety of topics, such as prevention strategies and functional communication training, throughout implementation of the RUBI protocol.
Primary Outcome Measure Information:
Title
Rate of Problem Behavior
Description
The investigators will collect continuous, direct-observation measures of destructive behavior throughout all phases of the study. They will compare rates of destructive behavior during assessment, treatment, caregiver training, and followup.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Caregiver report
Description
The investigators will compare caregiver reports of targeted problem behavior severity during treatment across the two experimental groups.
Time Frame
2 years
Title
Clinical Global Impressions Severity Subscale
Description
The investigators will compare the severity of targeted topographies of problem behavior during treatment across the two experimental groups using the Clinical Global Impressions Severity Subscale. Severity is rated on a seven-point scale, ranging from 1 (normal) to 7 (among the most severe).
Time Frame
2 years
Title
Aberrant Behavior Checklist Irritability Subscale
Description
The investigators will compare the generalized effects of treatment on both targeted and non-targeted problem behavior across both experimental groups using the Aberrant Behavior Checklist irritability Subscale. The irritability subscale contains 15 items. Irritability items are scored using a four-point scale, ranging from 0 (not at all a problem) to 3 (the problem is severe in degree). A higher composite score of all irritability items indicates greater severity.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: children from ages 3 to 17; challenging behavior that occurs at least 10 times a day, despite previous treatment; challenging behavior maintained by social positive or automatic reinforcement; stable protective supports for self-injurious behavior (e.g., helmet) with no anticipated changes during enrollment; 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 challenging 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 self-injury during study assessments that presents a risk of serious or permanent harm (e.g., detached retinas) based on our routine clinical-risk assessment (Betz, 2011); patients requiring changes to protective supports for self-injury or drug treatment, but we will invite these patients to participate when protective supports and drug regimen are stable.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wayne Fisher, PhD
Phone
8488008503
Email
wayne.fisher@rutgers.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Serena Claiborne
Phone
8488008504
Email
sclaibor@rutgers.edu
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
08873
Country
United States
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 Clairborne
Phone
8488008504
Email
sclaibor@rutgers.edu
First Name & Middle Initial & Last Name & Degree
Wayne Fisher, PhD

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.
Citations:
Citation
Bearss, K., Johnson, C. R., Handen, B. L., Butter, E., Lecavalier, L., Smith, T., & Scahill, L. (2018). Parent training for disruptive behavior: The RUBI autism network, clinician manual. Oxford University Press.
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Manualized Assessment and Treatment Model of Challenging Behavior

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