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Clinical Trials/NCT06584513
NCT06584513
Recruiting
Not Applicable

Implementing a Patient-centred and Evidence-based Intervention to Reduce BEnzodiazepine and Sedative-hypnotic Use to Improve Patient SAFEty and Quality of Care (BE-SAFE)

Insel Gruppe AG, University Hospital Bern6 sites in 6 countries470 target enrollmentNovember 18, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Benzodiazepines Deprescribing
Sponsor
Insel Gruppe AG, University Hospital Bern
Enrollment
470
Locations
6
Primary Endpoint
BSH discontinuation
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

Among older adults (≥65 years), use of sleeping pills, such as benzodiazepines and other sedative-hypnotics, to treat sleep problems is common. While sleeping pills are effective in the first few weeks of use, their effect diminishes significantly after that. Especially older adults are susceptible to significant adverse effects of sleep pills, yet stopping sleeping pills remains challenging. BE-SAFE aims to conduct a randomised study testing a patient-centred intervention to reduce sleeping pill use and to improve patient safety and quality of care focusing on implementation aspects. The intervention addresses knowledge and practice gaps related to discontinuation of sleeping pills in older adults with sleep problems.

Detailed Description

Background: Use of Benzodiazepine and Sedative Hypnotics (BSHs) is one of the three overuse practices measured by the OECD. BSH use has been reported to be as high as 15-30% in older adults with 87% taking BSHs for sleep problems. Use of BSHs is associated with significant adverse effects such as falls, fractures, hospitalisations, impaired functioning, delirium, dementia and mortality and therefore threatens patient safety. This applies especially to older adults as they are more susceptible to adverse effects due to changes in pharmacokinetics and pharmacodynamics associated with age and to the frequent presence of polypharmacy and comorbidities. Design: Multicenter, superiority (first co-primary endpoint) and non-inferiority (second co-primary endpoint) cluster randomised controlled trial (RCT) conducted in six countries across Europe (Belgium, Greece Norway, Poland, Spain, and Switzerland). Participating physicians will be randomly assigned in a 1:1 ratio in clusters to either the intervention group (with training and additional material to overcome sleeping problems and to help participants discontinue BSH) or the control group (treatment according to standard of care without training or additional material). Eligible patients will be enrolled with their treating physician defined as the cluster. Outcome assessment will be blinded.

Registry
clinicaltrials.gov
Start Date
November 18, 2024
End Date
February 1, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ≥65 years old
  • BSH (ATC codes N05BA, N05CF, N05CD, and N03AE01) use on average ≥3 times a week during the last 3 months prior to providing informed consent, as self-reported by the patient or by the informal carer
  • Taking BSH for sleep problems, as self-reported by the patient or by the informal carer

Exclusion Criteria

  • Indication for BSH appropriate or withdrawal dangerous, based on available documents (diagnosis list) or General Practitioner (GP) information:
  • Current use of BSH for alcohol withdrawal
  • BSH use in the context of addiction
  • Rapid Eye Movement (REM) sleep Behaviour Disorders
  • Active diagnosis of severe non-REM-related parasomnias with risk of self-damage or giving harm to others or with high frequency or social embarrassment
  • Epilepsy (all forms, because of risk of seizures by sleep deprivation)
  • Current active diagnosis of severe general or specific anxiety disorder (including obsessive compulsive disorder, social phobia, post-traumatic stress disorder, panic disorder with or without agoraphobia)
  • Current active diagnosis of psychotic disorder with or without antipsychotic medication
  • Current active diagnosis of severe depression with or without major anxiety symptoms
  • Current active diagnosis of bipolar disorder with or without major anxiety symptoms

Outcomes

Primary Outcomes

BSH discontinuation

Time Frame: 12 months after enrollment

Number of patients with BSH discontinuation according to self-/informal carer-disclosure. Discontinuation is defined as the intake of a maximum of one tablet within the previous 14 days.

Quality of sleep

Time Frame: 12 months after enrollment

Quality of sleep measured by the Insomnia Severity Index (ISI). The questionnaire consists of 7 questions, answers range from 0-4 points, which are added up to get a total score. The higher the total score, the more severe level of insomnia.

Secondary Outcomes

  • Use of a substitute medication for sleep(2 months, 6 months, and 12 months after enrollment)
  • BSH discontinuation discussion with HCP(1 month, 2 months, and 6 months after enrollment)
  • Benzodiazepines (BSH) discontinuation or dose reduction(2 months and 6 months after enrollment)
  • BSH adverse events(12 months after enrollment)
  • Quality of sleep(2 months and 6 months after enrollment)
  • BSH standardized daily dose intake(2 months, 6 months, and 12 months after enrollment)
  • Health-related quality of life(2 months, 6 months, and 12 months after enrollment)
  • Withdrawal symptoms from BSH discontinuation(2 months and 6 months after enrollment)

Study Sites (6)

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