Decreasing Destructive Behavior Clinical Trial
Official title:
Motivational Refinements for Facilitating Reinforcement Schedule Thinning
Destructive behavior represents a comorbid condition of developmental disability for which risk increases with intellectual disability severity, communication deficits, and co-occurring autism spectrum disorder. Destructive behavior, such as self-injurious behavior and aggression, causes harm to the child and others and increases the risk for institutionalization, social isolation, physical restraint, medication overuse, and abuse. Clinicians have used functional analyses to identify the variables that reinforce destructive behavior and to develop effective, function-based treatments. Functional communication training (FCT) is an empirically supported, function-based treatment that decreases destructive behavior. Using FCT, the clinician teaches the child to use a functional communication response (FCR) to request the reinforcer maintaining destructive behavior, while placing destructive behavior on extinction. For example, if functional analysis results showed that attention reinforced destructive behavior, the clinician would provide attention when the child used the FCR ("Play with me, please") and would not provide attention for destructive behavior. Two limitations of FCT are that (a) schedules of reinforcement maintaining the FCR must often be thinned gradually to levels that are practical for caregivers to implement consistently in the home and in the community, and (b) this necessary process of reinforcement schedule thinning regularly causes destructive behavior to increase following initially effective treatment, a form of treatment relapse called resurgence. The current project aims to improve these limitations of FCT by (a) hastening the process of reinforcement schedule thinning by removing unnecessary schedule-thinning steps using the results of a progressive interval assessment and (b) mitigating the resurgence of destructive behavior by providing stimuli that highly compete with the reinforcer maintaining destructive behavior. The investigators will conduct a randomized clinical trial to evaluate the extent to which these two promising refinements to FCT improve the process of reinforcement schedule thinning, and an exploratory experiment will examine the interactive effects of these two approaches. This novel project has the potential to substantially improve standards of care guiding the treatment of severe destructive behavior and to improve the long-term outcomes for children and families afflicted by these debilitating behavior disorders.
| Status | Recruiting |
| Enrollment | 30 |
| Est. completion date | August 31, 2028 |
| Est. primary completion date | May 31, 2028 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 3 Years to 17 Years |
| Eligibility | 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 - 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 destructive behavior - Diagnostic and Statistical Manual-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 routine clinical-risk assessment - patients requiring changes to protective supports for self-injury or drug treatment, but investigators will invite these patients to participate when protective supports and drug regimen are stable |
| Country | Name | City | State |
|---|---|---|---|
| United States | Douglass Developmental Disabilities Center | New Brunswick | New Jersey |
| United States | Rutgers University Center for Autism Research, Education, and Services | Somerset | New Jersey |
| Lead Sponsor | Collaborator |
|---|---|
| Rutgers, The State University of New Jersey |
United States,
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* Note: There are 16 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Destructive behavior (responses per minute) | The primary outcome measure is responses per minute of destructive behavior. The investigators will calculate this outcome by dividing the total number of destructive responses per session by the total number of minutes spent in session. | Through study completion, an average of 4 weeks. | |
| Primary | Discriminated functional communication responses (percentage) | The investigators will calculate this outcome by dividing the number of child requests when reinforcement is signaled as available by the total number of child requests during reinforcement and extinction, then multiplying the quotient by 100 to convert it to a percentage. This indicates the level of accuracy with communication requests, with 80-100% being optimal. | Through study completion, an average of 4 weeks. | |
| Primary | Efficiency of schedule thinning | In addition to the above metrics, it is expect that informing schedule thinning with the PIA or competing items may result in reaching the terminal schedule (e.g., 270-s extinction) more rapidly than conditions not so informed. Thus, investigators will analyze the number of treatment sessions required for an intervention to produce destructive behavior below an 85% reduction from baseline and discriminated functional communication responses above 80% at the terminal-schedule value. | Through study completion, an average of 4 weeks. |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT03423940 -
Resurgence as Choice: Basic and Clinical Studies
|
N/A |