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RAPD Strategy for Substance Abuse (RAPD Trial)

N/A

Waitlist Available

Led By Andria Eisman, PhD

Research Sponsored by Wayne State University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 9 months

Awards & highlights

RAPD Trial Summary

This trial compares two strategies to help Michigan Middle Schools improve health & wellness: standard & RAPD strategies.

Who is the study for?

This trial is for Michigan middle schools with 7th-grade classes that have at least 25% of students eligible for free/reduced meals and are struggling to meet state standards for health curriculum implementation.Check my eligibility

What is being tested?

The study compares two strategies: the usual way schools implement drug prevention programs versus a new, rapid adaptation method. Schools will be randomly assigned to one of these groups in equal numbers.See study design

What are the potential side effects?

Since this trial involves educational strategies rather than medical treatments, there aren't traditional side effects. However, unintended consequences may include changes in school resources or staff workload.

RAPD Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 9 months

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~9 months

This trial's timeline: 3 weeks for screening, Varies for treatment, and 9 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

RAPD Strategy Acceptability

RAPD Strategy Appropriateness

RAPD Strategy Feasibility

Secondary outcome measures

MMH Fidelity

RAPD Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: Rapid Adaptation to Prevent Drug Use (RAPD)Experimental Treatment1 Intervention

RAPD is a novel bundle of implementation strategies to improve the responsiveness of an existing evidence-based intervention (EBI), the Michigan Model for Health (MMH) for urgent drug events. These implementation strategies will be deployed in addition to standard implementation components.

Group II: Standard Michigan Model for Health (MMH) Curriculum ImplementationActive Control1 Intervention

Standard implementation of the MMH (Michigan Model for Health), a universal prevention intervention includes curriculum materials, foundational curriculum training and as-needed technical assistance, provided by the regional school health coordinators.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

National Institute on Drug Abuse (NIDA)NIH

2,464 Previous Clinical Trials

2,618,581 Total Patients Enrolled

153 Trials studying Substance Abuse

707,142 Patients Enrolled for Substance Abuse

Wayne State UniversityLead Sponsor

307 Previous Clinical Trials

108,452 Total Patients Enrolled

5 Trials studying Substance Abuse

948 Patients Enrolled for Substance Abuse

Andria Eisman, PhDPrincipal InvestigatorWayne State University

Media Library

Rapid Adaptation to Prevent Drug Use (RAPD) Clinical Trial Eligibility Overview. Trial Name: NCT05806840 — N/A

Substance Abuse Research Study Groups: Standard Michigan Model for Health (MMH) Curriculum Implementation, Rapid Adaptation to Prevent Drug Use (RAPD)

Substance Abuse Clinical Trial 2023: Rapid Adaptation to Prevent Drug Use (RAPD) Highlights & Side Effects. Trial Name: NCT05806840 — N/A

Rapid Adaptation to Prevent Drug Use (RAPD) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05806840 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is enrollment open to participate in this investigation?

"Acceptance to this trial necessitates a history of substance abuse, and participants must be between 11 and 99 years old. Currently 12 individuals are being sought out for the study."

Answered by AI

Is this study open to individuals who are over the age of 45?

"This research programme has established that the ideal participants should range between 11 and 99 years old. There are 72 trials for those under 18, while 254 trials have been opened up to seniors over 65."

Answered by AI

Are there still slots open for participation in this investigation?

"The information accessible on clinicaltrials.gov reveals that the study is not taking applications presently. Initially listed on August 1st 2023, with its last edit being April 6th 2023, this trial has ceased to recruit patients; however, there are currently 356 other trials actively seeking participants."

Answered by AI

Recent research and studies

Implementation ScienceJournal

Psychometric Assessment of Three Newly Developed Implementation Outcome Measures

Weiner, Bryan J., Cara C. Lewis, Cameo Stanick, Byron J. Powell, Caitlin N. Dorsey, Alecia S. Clary, Marcella H. Boynton, and Heather Halko. 2017. “Psychometric Assessment of Three Newly Developed Implementation Outcome Measures”. Implementation Science. Springer Science and Business Media LLC. doi:10.1186/s13012-017-0635-3.

Implementation ScienceJournal

The FRAME: An Expanded Framework for Reporting Adaptations and Modifications to Evidence-based Interventions

Wiltsey Stirman, Shannon, Ana A. Baumann, and Christopher J. Miller. 2019. “The FRAME: An Expanded Framework for Reporting Adaptations and Modifications to Evidence-based Interventions”. Implementation Science. Springer Science and Business Media LLC. doi:10.1186/s13012-019-0898-y.

clinicaltrials.govStudy

Rapid Adaptation to Prevent Drug Use

Andria B Eisman 2023. "Rapid Adaptation to Prevent Drug Use". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05806840.

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