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Testing a new intervention to support people who are dependent on opiate and benzodiazepine drugs

Developing an intervention to manage benzodiazepine dependence and high-risk use in the context of escalating drug deaths: a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN95130898
Enrollment
45
Registered
2023-10-23
Start date
2022-05-01
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High-risk illicit drug use Mental and Behavioural Disorders

Interventions

The intervention tested was a prescription of diazepam at a maximum dose of 30 mg, and a fortnightly nurse session addressing: anxiety, sleep and pain management and harm reduction support to reduce h

Sponsors

University of Stirling
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. People in NHS drug treatment services who have achieved a stable dose of ORT (methadone or buprenorphine) 2. Have the capacity to provide informed consent 3. Experiencing ongoing risk of harm from street benzodiazepine use. ‘Risk of harm’ was defined as: an overdose event in the last 6 months in which a street benzodiazepine was implicated (from toxicology or clinical profile) and/or persistent self-report of daily street benzo use that is confirmed by toxicology screening and/or self-report of regular use of high doses/quantities of street benzodiazepines

Exclusion criteria

Exclusion criteria: 1. Co-occurring harmful alcohol use 2. Co-occurring harmful stimulant use 3. Pregnancy 4. Participation in any other research study 5. Diagnosed serious mental illness or severe cognitive impairment that clinical staff consider poses a risk to safety (of patient or staff) 6. Non-English speaking 7. People who do not have the capacity to provide informed consent 8. ‘Harmful’ alcohol or stimulant use was use at a level in which it was the dominant problem for that individual

Design outcomes

Primary

MeasureTime frame
Use of illicit benzodiazepines measured using self-report and oral fluid testing monthly during the study

Secondary

MeasureTime frame
1. Cognitive ability assessed using Addenbrooke's Cognitive Evaluation (ACE III) at baseline & follow-up (6 months) 2. Quality of life assessed using EQ5D-5L monthly during the study 3. Anxiety assessed using General Anxiety Disorder (GAD-7) at baseline & follow-up (6 months) 4. Depression assessed using Patient Health Questionnaire-9 (PHQ-9) at baseline & follow-up (6 months) 5. Self-assessed substance use recovery assessed using SURE questionnaire at baseline & follow-up (6 months) 6. Economic evaluation using NHS service use questionnaire completed monthly during the study 7. Satisfaction with professional care assessed using Consultation and Relational Empathy Measure (CARE) at follow-up (6 months)

Countries

Scotland, United Kingdom

Contacts

Public ContactCatriona Matheson
catriona.matheson@stir.ac.uk+44 (0)7870135667

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026