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

NCT05189223 · ClinicalTrials.gov registry record · NA

A Brief Values Intervention to Support Veterans in Early Buprenorphine Treatment

A NA study of Dependence, Opioid, sponsored by VA Office of Research and Development.

Recruiting
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT05189223: Recruiting NA study of Dependence, Opioid, sponsored by VA Office of Research and Development.

NCT05189223 is a NA study of Dependence, Opioid that is actively recruiting participants, run by VA Office of Research and Development. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05189223, a NA study of Dependence, Opioid, is actively recruiting participants, sponsored by VA Office of Research and Development.

RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

The US Veteran community continues to feel the impact of the overdose crisis, and opioid use disorder (OUD) diagnoses among Veterans continue to rise. Medication treatment (e.g., buprenorphine, methadone, naltrexone) helps prevent relapse and reduce overdose risk, but does not help with the psychological, social, and functional challenges of early recovery. Therapies that focus on interpersonal functioning and community integration may help improve quality of life during this high-risk period. This research project will create and test a brief, values-based treatment to help Veterans improve their interpersonal functioning and community integration during early treatment. This study will have three phases. Phase 1 will involve the development of the treatment and adaptation using interviews with Veterans and VA Providers. Phase 2 will test the treatment with a group of 10 Veterans to make sure the treatment can be delivered as intended, and to make changes to the treatment or study procedures based on Veteran feedback. Finally, Phase 3 will test the treatment compared to usual treatment in a pilot randomized controlled trial with a group of 40 Veterans. This final phase will provide additional information about Veterans' experience of the treatment and study procedures and the preliminary effects of the treatment on quality of life and related outcomes.

Primary Outcome

The Credibility/Expectancy Questionnaire (CEQ) is a 6-item self-report measure which will be administered following the first intervention session. Expectancy will be measured using item 4, the most common index for expectancy. This item is rated on a scale from 0% to 100% with higher percentages reflecting higher anticipated improvement. As an indicator of acceptability of the intervention in Phase 3, the investigators will use a priori benchmark of average expectancy at or above 50%. improveme

Conditions Studied

Interventions

  • BEHAVIORAL Treatment as Usual
  • BEHAVIORAL Brief, values based intervention for early buprenorphine treatment

Study Locations (1)

Massachusetts

  • VA Bedford HealthCare System, Bedford, MA - Bedford

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-09-01
Est. Completion 2027-03-31
Phase NA
VA Office of Research and Development

1,668 total trials

What NCT05189223 shows while recruiting

NCT05189223 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Dependence, Opioid appearing as the primary indexed condition, and to 2 interventions - of which Treatment as Usual is the first listed.

NCT05189223 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT05189223 about?

NCT05189223 is a clinical study titled "A Brief Values Intervention to Support Veterans in Early Buprenorphine Treatment". The US Veteran community continues to feel the impact of the overdose crisis, and opioid use disorder (OUD) diagnoses among Veterans continue to rise. Medication treatment (e.g., buprenorphine, methadone, naltrexone) helps prevent relapse and reduce overdose risk, but does not help with the psycholo...

What is the current status of trial NCT05189223?

This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2023-09-01. Estimated completion is 2027-03-31.

What conditions does trial NCT05189223 study?

This clinical trial studies the following conditions: Dependence, Opioid.

What interventions are being tested in trial NCT05189223?

The interventions under investigation include: Treatment as Usual (BEHAVIORAL), Brief, values based intervention for early buprenorphine treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT05189223?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05189223 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT05189223's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 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

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05189223, the US trial registry maintained by the National Library of Medicine. NCT05189223 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.