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A open trial evaluation of the Benzodiazepine (information and reduction) eHealth program (BDZ eHealth) for people using benzodiazepines.

A open trial evaluation of the BDZ (information and reduction) eHealth program to reduce benzodiazepine usage and decrease negative affect for Australian adults using benzodiazepines.

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000479505
Enrollment
32
Registered
2015-05-14
Start date
2015-09-04
Completion date
2017-06-09
Last updated
2022-08-09

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

Conditions

None listed

Brief summary

A simple open trial will be used to evaluate the effectiveness of the Benzodiazepine eHealth program (BDZ eHealth) that provides psycho-education and gradual reduction information. BDZ eHealth can be accessed on multiple devices (desk top, tablet and mobile). People, who visit the website, either directly or through seeing the study advertised, will be invited to take part in the BDZ eHealth evaluation study. BDZ eHealth is designed to provide people with information and strategies to address their benzodiazepine use via five ‘core’ modules, plus an Introduction module. Each module will take approximately 20 minutes to complete. Participants will receive automated emails (e.g., on completion of a module, when to complete post/follow-up questionnaires) and will be asked several questions at the beginning of each week, to monitor their progress and activities. During the course of the study we strongly encourage participants to work with their doctor should they decide to reduce their benzodiazepine dosage as well as seek specialist benzodiazepine telephone support from Reconnexion. Participants will complete a pre-intervention assessment (Week 0), during intervention (Week 1 - 5) assessments, a post-intervention assessment (Week 6) and a 1 and 3 month follow-up assessment (Week 10 & Week 18 respectively). Participants will continue to have access to the program for the duration of the trial. Participants will be asked questions to ascertain reasons for engagement or lack of engagement with the program. It is expected that people who undertake BDZ eHealth will show reductions in their benzodiazepine dependency, anxiety and / or depressive symptoms at post and follow-up time points

Interventions

A simple open trial will be used to evaluate the effectiveness of the Benzodiazepine eHealth program (BDZ eHealth) that provides psycho-education and gradual reduction information. BDZ eHealth is designed to provide people with information and strategies to address their benzodiazepine use via five ‘core’ modules, plus an Introduction module. The BDZ eHealth has five core modules are: 1. Benzodiazepines and Dependence: This module provides psycho-education around what BDZs are, dependency on

A simple open trial will be used to evaluate the effectiveness of the Benzodiazepine eHealth program (BDZ eHealth) that provides psycho-education and gradual reduction information. BDZ eHealth is designed to provide people with information and strategies to address their benzodiazepine use via five ‘core’ modules, plus an Introduction module. The BDZ eHealth has five core modules are: 1. Benzodiazepines and Dependence: This module provides psycho-education around what BDZs are, dependency on BDZ, BDZ effectiveness and appropriate and inappropriate uses of BDZ. 2. The Pathway to Reduction: This module provides psycho-education on BDZ reduction and withdrawal processes, involving the 3 main steps in the BDZ reduction process 3. A Gradual Reduction Program (Case Illustration). This third module provides an illustrative case example of ‘Peter’ outlining his gradual benzodiazepine reduction program over time. 4. Withdrawal Symptoms. This module provides information around what BDZ related withdrawal symptoms are, common and uncommon withdrawal symptoms, and the issues with going ‘cold turkey’. 5. Managing Withdrawal Symptoms: This module contains information and helpful strategies to help manage the reduction/withdrawal symptoms (e.g., controlled breathing, progressive muscle relaxation, mindfulness meditation, problem solving, goal setting, increasing physical exercise, nutrition, sleep hygiene). All modules are open from the first log in and each module will take approximately 20 minutes to complete. Participants are encouraged to first read the Introduction module and then work through the other program modules at their own pace, over the 5 weeks. Given the open access nature of the program modules, participants are free to choose whether they work through the modules sequentially or not. Participants will receive automated emails (e.g., to log on, when to complete post/follow-up questionnaires) and will be asked several questions at the beginning of each week, to monitor their progress and activities. Modules make use of text, graphics, audio, video, editable forms and downloads. Modules can be accessible via web, mobile or tablet devices. We also encourage participants to make use of the Reconnexion benzodiazepine telephone support service while undertaking the BDZ eHealth program, as well as work in conjunction with their doctor should they wish to commence benzodiazepine reduction. Participants will complete a pre-intervention assessment (Week 0), during intervention (Week 1 - 5) assessments, a post-intervention assessment (Week 6) and a 1 and 3 month follow-up assessment (Week 10 & Week 18 respectively). Participants will continue to have access to the program for the entire duration of the trial. Participants will also be asked to complete a short online questionnaire to determine the reasons for their engagement/disengagement with the program.

Sponsors

Federation Unversity
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must be 18 years or older, currently using benzodiazepines, have access to the internet, provide consent, and be able to register online using an email address.

Exclusion criteria

Participants must not be residing overseas, do not have a current untreated and severe (psychotic) illness, nor will they be using the ‘cold turkey’ method to reduce their benzodiazepine intake during the study (i.e., complete withdrawal from their benzodiazepines).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026