Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00430482 · ClinicalTrials.gov registry record · NA

Stress, Distress Intolerance, and Drug Dependence

A NA study, sponsored by Boston University Charles River Campus.

Completed
Registry status
NA
Development phase
133
Enrollment target

NCT00430482: Completed NA study, sponsored by Boston University Charles River Campus.

NCT00430482 is a NA study that has completed, run by Boston University Charles River Campus. The registered enrollment target is 133 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00430482, a NA study, has completed, sponsored by Boston University Charles River Campus.

COMPLETED
Registry status
NA
Development phase
133 participants
Enrollment target

Study Summary

This study is designed to evaluate the relative efficacy of a novel treatment (CBT-IC) versus a standard individual drug-counseling treatment. The novel treatment emphasizes exposure to emotional cues for drug use as part of a comprehensive, yet brief, treatment strategy. These treatments are delivered to opiate-dependent, often poly-substance dependent, individuals in a comprehensive methadone maintenance program who have failed to respond adequately to current treatments.

Primary Outcome

The primary outcome assessment for this study was the percentage of oral toxicology swabs that were positive of illicit substances. Participants completed these swabs at each assessment point, as well as at each study therapy session. Toxicology swabs were supervised by study staff and used oral specimen collection to screen for opiates, methadone, cocaine, benzodiazepines, amphetamines, THC, and barbiturates.

Interventions

  • BEHAVIORAL Cognitive Behavioral Therapy
  • BEHAVIORAL Individual Counseling

Trial Details

FieldValue
Enrollment Target 133 participants
Start Date 2005-06
Est. Completion 2011-07
Phase NA

What the finished NCT00430482 record still lists

NCT00430482 is an interventional study that assigns participants to a tested intervention. The registered 133 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 2 interventions - of which Cognitive Behavioral Therapy is the first listed.

NCT00430482 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00430482 about?

NCT00430482 is a clinical study titled "Stress, Distress Intolerance, and Drug Dependence". This study is designed to evaluate the relative efficacy of a novel treatment (CBT-IC) versus a standard individual drug-counseling treatment. The novel treatment emphasizes exposure to emotional cues for drug use as part of a comprehensive, yet brief, treatment strategy. These treatments are delive...

What is the current status of trial NCT00430482?

This trial is currently completed. It is a NA study. The enrollment target is 133 participants. The study started on 2005-06. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00430482?

The interventions under investigation include: Cognitive Behavioral Therapy (BEHAVIORAL), Individual Counseling (BEHAVIORAL).

Who is sponsoring clinical trial NCT00430482?

This trial is sponsored by Boston University Charles River Campus, which has 104 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00430482's enrollment target sits among peer trials

133 729th of 2000 higher than 1,272 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04276870 · 133 participants · Phase 2

    Orphan Indications for CD19 Redirected Autologous T Cells

  • NCT04671771 · 133 participants · NA

    A Study to Evaluate the Safety and Effectiveness of the InnAVasc Arteriovenous Graft for Hemodialysis Access in Patients With End-Stage Renal Disease

  • NCT05610085 · 133 participants · Phase 2

    A Dose Escalation Study of Levetiracetam in the Treatment of Neonatal Seizures

  • NCT06206486 · 133 participants

    The Gut Microbiome and Serum Metabolites As a Biological Mechanism Underlying Pain in Kidney Transplantation

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00430482, the US trial registry maintained by the National Library of Medicine. NCT00430482 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.