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Starting soon Not applicable

Early Addiction Care Pathway After Acute Drug Intoxication in Emergency Departments

NCT07738835 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-10-15
Last updated
2026-07-31

Condition(s) studied

Intoxication; Opioid

Investigational drug(s) / intervention(s)

Structured early addiction careNot structured early addiction care

Structured early addiction care: The intervention consists of a structured early addiction care program initiated during hospitalization for acute psychoactive substance intoxication. It includes: * A standardized addiction consultation during the index hospitalization; * A protocolized follow-up schedule over 6 months, with 1-2 structured contacts per month (in-person or telephone); * Systematic harm reduction assessment and counseling at predefined visits; * Collection and structured feedback of toxicological results (urine, blood, and hair samples), including discussion of discrepancies between declared and detected substance use; * Reinforcement of linkage to addiction services and maintenance in the care pathway. The intervention aims to enhance patient engagement, insight into substance use patterns, and long-term retention in addiction care.

Not structured early addiction care: The intervention consists of a streamlined consultation with the implementation of addiction follow-up, possibly via video and telephone, and "treatment as usual" with routine toxicology tests typically used in most emergency departments. This program includes: * A standardized addiction consultation during initial hospitalization; * Addiction follow-up with random interviews and/or workshops, at least once a month, lasting 6 months or at the patient's request; * A systematic harm reduction assessment and support during pre-defined consultations, without taking into account the results of hair samples tests; * Collection of toxicology results (hair follicle), including a discussion of discrepancies between reported and detected substance use, at the end of the study at month 6.

Study summary

Acute intoxication with psychoactive substances represents a major public health issue and a frequent reason for emergency department (ED) visits. Beyond the acute medical management of intoxication, one of the main challenges remains the continuity of addiction care after discharge. Many patients disengage rapidly from follow-up services, leading to recurrent intoxication episodes, repeated ED admissions, and increased morbidity.

The IPAIS study (Interventions Précoces en Addictologie dans le cadre des urgences par Intoxications aiguës aux Stupéfiants) is a multicenter, randomized, parallel-group, open-label clinical trial designed to evaluate whether an enhanced early addiction care pathway improves retention in addiction treatment among patients admitted to emergency departments for acute intoxication involving at least one illicit psychoactive substance (excluding isolated alcohol intoxication).

All participants will receive an early addiction consultation within 24 to 72 hours following the acute event. In the experimental group, this consultation will be combined with a structured and standardized feedback session on toxicological analysis results and a proactive follow-up strategy including scheduled telephone contacts over a 6-month period. The control group will receive early addiction consultation according to usual care procedures, without the structured feedback and standardized follow-up program implemented in the experimental arm.

The primary objective of the study is to determine whether the enhanced intervention improves retention in the addiction care pathway at 6 months after inclusion. Retention is defined as sustained engagement in addiction care, operationalized as at least one addiction-related consultation per month and/or regular telephone-based addiction follow-up over the 6-month period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Patients admitted and/or hospitalized in the emergency department or intensive care unit following acute poisoning must: * Be over 18 years of age * Have consumed at least one identifiable non-alcoholic narcotic, including psychoactive substances detected by standard urine drug screening (dipstick) * Have a history of using at least one non-alcoholic psychoactive substance within the last 30 days * Speak and understand French * Have at least 1 cm of hair * Be covered by a social security scheme (member or dependent) * Be the patient or a relative/close contact/trusted person who has been informed about the study and has given their informed consent (or completed the emergency inclusion procedure) * Have a mobile phone number or email address to be contacted Exclusion Criteria: * Acute suicidal crisis requiring priority psychiatric care * Acute alcohol intoxication (after confirmation by urine drug screening in the Emergency Department) * Acute episode related to exclusive opiate use, requiring opiate substitution therapy * Prolonged hospitalization in intensive care or follow-up care due to complications of alcohol intoxication beyond 8 days after the initial addiction assessment * Protected patient: under a valid legal guardianship, curatorship, or conservatorship * Patient requiring involuntary psychiatric hospitalization

Primary outcome measure(s)

  • Retention in addiction care at 6 months — 6 months after randomization
    Proportion of randomized participants who are still actively engaged in a structured addiction care pathway 6 months after randomization. Retention is defined as attendance at ≥1 scheduled addiction care contact (in-person visit, structured psychological session, or protocol-defined telephone follow-up) within the predefined follow-up window around Month 6 (±30 days), without documented loss to follow-up or withdrawal from addiction care.

Trial sites (4)

FacilityCityRegionStatus
Hôpital Saint Antoine Paris France
Unité d'Addictologie Hospitalière/ELSA Hôpital Pitié Salpêtrière Paris France
Hôpital Tenon Paris France
hôpital kremlin Bicêtre Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07738835 on ClinicalTrials.gov ↗ ← All trials in France