Trial of online support for primary care patients tapering off antidepressant medicatio
- Conditions
- Decreasing antidepressant (AD) medication for depressionMental and Behavioural Disorders
- Registration Number
- ISRCTN11562922
- Lead Sponsor
- niversity of Melbourne
- Brief Summary
2024 Other publications in https://pubmed.ncbi.nlm.nih.gov/38355180/ (added 15/02/2024)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 312
1. 18-75 years
2. Stable on AD for >=12m: (no depressive episodes)
3. No history of recurrent depression
4. Sufficient English language proficiency to provide informed consent
5. No or mild depressive symptoms as measured on the Personal Health Questionnaire (PHQ9)
6. Low risk of Suicide or Self-harm
7. Agree to consider reviewing their AD use
8. Agree to be randomized into the study
9. Willing to provide informed consent
1. Those currently experiencing a major life event in the next 3 months
2. Currently using ADs for any other health condition (other than depression)
3. Currently using non-SSRI or SNRI ADs, antipsychotics, or other mood stabiliser medication
4. Have no daily access to the internet
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of patients successfully ceasing ADs at 6 months where successful cessation is defined as no AD use (as measured by the Resource Use Questionnaire (RUQ)) and the absence of clinically significant depressive symptoms (as measured by the Patient Health Questionnaire 9-item (PHQ-9)). Measured at 3-, 6-, 12-, 18-months post-baseline. Primary outcome is at 6-months post baseline.
- Secondary Outcome Measures
Name Time Method