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Enrolling By Invitation NCT07693439

Implementing DBT in Short-Term SUD-treatment

Conditions: Substance Abuse Disorder, Dialectical Behavior Therapy, Emotion Management Skills

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 82
Sponsor: Helse Møre og Romsdal HF

Location: Helse Møre og Romsdal HF Ålesund More and Romsdal

Summary

The main objective of the study is to provide new knowledge about the implementation of DBT-informed environmental therapy in short-term substance use disorder (SUD) inpatient treatment. The study will examine which organizational and clinical conditions promote or inhibit implementation in clinical practice by elucidating how the implementation is experienced by staff (including experiences with structure, skill focus and environmental therapeutic principles) related to DBT-informed environmental therapy, DBT-SUD skill groups and patients' perceived satisfaction and utility. A secondary and exploratory aim is to examine preliminary trends in clinical measures in patients over time, including changes in symptom burden and reported use of DBT skills throughout the course of treatment. The study further seeks, at a descriptive and hypothesis-generating level, to explore patterns in patient-reported conditions related to substance abuse, emotion regulation, and other clinical burden. The sample will consist of up to 70 adult patients and 12 staff. One half of the patients will receive ordinary short-term inpatient treatment, while the other half will receive DBT informs milieu therapy after the approach has been established in clinical practice without being implemented. All patients will complete questionnaires upon admission (baseline), week 6 and upon discharge (week 12).

Eligibility Criteria

Inclusion Criteria Adults aged 18 years or older. Admitted to the participating short-term inpatient substance use disorder treatment unit during the study period. Able and willing to provide written informed consent. Exclusion Criteria Unable to understand study information. Unable to provide informed consent. Severe cognitive impairment or other conditions preventing meaningful participation in study procedures.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07693439). StuddyBuddy aggregates publicly available trial information.