Substance-related Disorders Clinical Trial
Official title:
Multimodal Treatment Study of Children With ADHD
This trial is a continuation of the Multimodal Treatment Study of Children with Attention
Deficit Hyperactivity Disorder (MTA Study). Continuation Aim 1 is to track the persistence
of intervention-related effects as the MTA sample matures into mid-adolescence, including
subsequent mental-health and school-related service utilization patterns as a function of
MTA treatment experience (treatment assignment) and outcome (degree of treatment success at
14 mo.). Aim 2 is to test specific hypotheses about predictors, mediators, and moderators of
long-term outcome among children with ADHD (e.g., comorbidity; family functioning; cognitive
skills; peer relations) that may influence adolescent functioning (either independent of or
through initial treatment assignment and/or 14-month treatment outcomes); and to compare how
these predictors, mediators, and moderators are similar or dissimilar within the normal
comparison group. Aim 3 is to track the patterns of risk and protective factors (including
their mediation or moderation by initial treatment assignment and/or outcome) involved in
early and subsequent stages of developing substance-related disorders and antisocial
behavior. Aim 4 is to examine the effect of initial treatment assignment and degree of
treatment success on later academic performance, achievement, school conduct, tendency to
drop out, and other adverse school outcomes.
In the original MTA design, patients were randomly assigned to 1 of 4 treatment conditions:
(1) medication only; (2) psychosocial only; (3) combined (medication and psychosocial); or
(4) Assessment-and-Referral condition. All but the latter were treated intensively for 14
months, with assessments for all subjects at baseline, 3, 9, 14, and 24 months. The original
MTA design thus provides short-term (10 months post-treatment) follow-up at 24 months. This
continuation extends the follow-up to assessments at 36, 60, and 84 months after treatment.
A child may be eligible for this study if he/she:
Is 7 - 9 years old, and has Attention Deficit Hyperactivity Disorder (ADHD).
This trial is a continuation of the Multimodal Treatment Study of Children with Attention
Deficit Hyperactivity Disorder (MTA Study). Continuation Aim 1 is to track the persistence
of intervention-related effects as the MTA sample matures into mid-adolescence, including
subsequent mental-health and school-related service utilization patterns as a function of
MTA treatment experience (treatment assignment) and outcome (degree of treatment success at
14 mo.). Aim 2 is to test specific hypotheses about predictors, mediators, and moderators of
long-term outcome among children with ADHD (e.g., comorbidity; family functioning; cognitive
skills; peer relations) that may influence adolescent functioning (either independent of or
through initial treatment assignment and/or 14-month treatment outcomes); and to compare how
these predictors, mediators, and moderators are similar or dissimilar within the normal
comparison group. Aim 3 is to track the patterns of risk and protective factors (including
their mediation or moderation by initial treatment assignment and/or outcome) involved in
early and subsequent stages of developing substance-related disorders and antisocial
behavior. Aim 4 is to examine the effect of initial treatment assignment and degree of
treatment success on later academic performance, achievement, school conduct, tendency to
drop out, and other adverse school outcomes.
In the original MTA design, patients were randomly assigned to 1 of 4 treatment conditions:
(1) medication only; (2) psychosocial only; (3) combined (medication and psychosocial); or
(4) Assessment-and-Referral condition. All but the latter were treated intensively for 14
months, with assessments for all subjects at baseline, 3, 9, 14, and 24 months. The original
MTA design thus provides short-term (10 months post-treatment) follow-up at 24 months. This
continuation extends the follow-up to assessments at 36, 60, and 84 months after treatment.
;
Allocation: Randomized, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05054738 -
CRP and S&A for Inpatient Veterans
|
N/A | |
Recruiting |
NCT04157062 -
An Open-Label Trial of Repetitive Transcranial Magnetic Stimulation for Opioid Use Disorder
|
N/A | |
Completed |
NCT02233738 -
Group Motivational Interviewing (GMI) For Homeless Veterans In VA Services
|
N/A | |
Enrolling by invitation |
NCT06084221 -
Fatal Overdose Review Teams - Research to Enhance Surveillance Systems
|
N/A | |
Completed |
NCT02907944 -
Working With HIV Clinics to Adopt Addiction Treatments Using Implementation Facilitation
|
N/A | |
Completed |
NCT02570360 -
Exercise and Treatment-as-usual in Substance Use Treatment Outcomes
|
N/A | |
Completed |
NCT02829970 -
Helping College Students With ADHD Lead Healthier Lifestyles
|
N/A | |
Completed |
NCT02945371 -
Tailored Inhibitory Control Training to Reverse EA-linked Deficits in Mid-life
|
N/A | |
Completed |
NCT02388243 -
The Computer-based Drug and Alcohol Training Assessment in Kenya
|
N/A | |
Completed |
NCT02715557 -
Arise: An Online Relapse Prevention Tool for Adolescent Substance Abusers
|
N/A | |
Completed |
NCT02125539 -
Field Trial of a Relapse Prevention Program for Adolescents Receiving Substance Use Treatment
|
Phase 2 | |
Completed |
NCT01633138 -
Performance-based Reinforcement to Enhance Cognitive Remediation Therapy
|
N/A | |
Completed |
NCT02218970 -
The Effect of Muscular Strength Training in Patients With Drug Addiction
|
N/A | |
Completed |
NCT01591239 -
Home-Based Program to Help Parents of Drug Abusing Adolescents
|
N/A | |
Active, not recruiting |
NCT01539525 -
Screening to Augment Referral to Treatment- Project START
|
Phase 2 | |
Withdrawn |
NCT01224002 -
A Comparative Feasibility Study to Assess the Prevalence and Severity of Dental Caries in Incarcerated People Who Abuse Methamphetamine
|
N/A | |
Withdrawn |
NCT00891631 -
Primary Care iSBIRT to Reduce Serious Teen Health Risks
|
Phase 1/Phase 2 | |
Completed |
NCT00970372 -
Dual-Diagnosis and Compulsory Treatment
|
N/A | |
Completed |
NCT01365247 -
Concurrent Treatment for Substance Dependent Individuals With Post-Traumatic Stress Disorder (PTSD)
|
N/A | |
Completed |
NCT00419029 -
Motivational Interviewing to Engage Operations Enduring Freedom and Iraqi Freedom (OEF/OIF) Veterans in Mental Health Treatment
|
N/A |