Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12609000559213
Ethics application status
Approved
Date submitted
3/07/2009
Date registered
9/07/2009
Date last updated
3/12/2015
Type of registration
Prospectively registered

Titles & IDs
Public title
Internet-based treatment of depression (the Sadness program): A randomized controlled study exploring the role of a clinician.
Scientific title
A randomized controlled trial comparing clinician-assisted Internet based treatment for depression vs. weekly telephone reminders vs. a waitlist control condition on severity of symptoms of depression.
Secondary ID [1] 288061 0
Nil
Universal Trial Number (UTN)
Trial acronym
Sadness RCT2
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Depression 237157 0
Condition category
Condition code
Mental Health 237483 237483 0 0
Depression

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Participants will be randomly assigned to one of three groups: 1) Treatment with clinician-assisted Internet based treatment for depression, or; 2) Treatment with self-guided Internet based treatment for depression + weekly reminder telephone calls from a technician, or; 3) Waitlist control. All participants will meet Diagnostic and Statistical Manual of Mental Disorders 4th Edition (DSM-IV) criteria for depression. All group 1 and group 2 participants will complete 6 lessons of Internet based treatment about the management of symptoms of depression. One lesson will be completed every 7 to 14 days. Each lesson will take about 15 minutes to complete. Group 1 participants will have access to summaries of each lesson, will contribute to an online forum moderated by a clinical psychologist or psychiatrist, and will receive weekly reminder emails. Group 2 participants will have access to summaries of each lesson, will receive weekly telephone reminders from a technician, and will receive weekly reminder emails. The duration of the program is 8 weeks, but participants will be contacted 2 and 4 months post program and asked to complete follow-up questionnaires. Study questionnaires will be administered at application, pre-treatment, post-treatment, and at 2 and 4-months post-treatment. These will take about 20 minutes to complete. The treatment materials are based on cognitive behavioural techniques.
Intervention code [1] 236871 0
Treatment: Other
Comparator / control treatment
Waitlist control group. These participants remain on the waitlist until the treatment groups have completed their treatment (8 weeks). At that time (8 weeks) the waitlist group will receive the same treatment as Treatment Group 1.
Control group
Active

Outcomes
Primary outcome [1] 238289 0
Symptoms and severity of depression is measured by the Patient Health Questionnaire-9 (PHQ-9).
Timepoint [1] 238289 0
Administered at application, pre-treatment, post-treatment, and at 2 and 4-months post-treatment.
Primary outcome [2] 238290 0
Symptoms and severity of depression is measured by the Beck Depression Inventory - II (BDI-II).
Timepoint [2] 238290 0
Administered at pre-treatment, post-treatment, and at 2 and 4-months post-treatment.
Secondary outcome [1] 244663 0
Psychological distress is measured by the Kessler-10 (K-10).
Timepoint [1] 244663 0
Administered at pre-treatment, post-treatment, and at 2 and 4-months post-treatment.
Secondary outcome [2] 244664 0
Disability is measured by the Sheehan Disability Scale.
Timepoint [2] 244664 0
Administered at pre-treatment, post-treatment, and at 2 and 4-months post-treatment.
Secondary outcome [3] 244665 0
Anxiety is measured by the Generalized Anxiety Disorder - 7 Item (GAD-7) questionnaire.
Timepoint [3] 244665 0
Administered at application, pre-treatment, post-treatment, and at 2 and 4-months post-treatment.

Eligibility
Key inclusion criteria
Meet Diagnostic and Statistical Manual of the American Psychiatric Association-4th Edition (DSM-IV) criteria for depression - Internet access + printer access. - Australian citizen- Males and females
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Current substance abuse/dependence- Psychotic disorder- Current or planned psychological treatment during study duration- Change in medications during last 1 month or intended change during study duration

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants apply on line, followed by a telephone interview to confirm diagnosis via the Mini-International Neuropsychiatric
Interview (MINI 5.0.0), a structured diagnostic interview. Participants will be randomized using a list generated prior to the study. Allocation concealment will occur by contacting the holder of the allocation schedule who is off-site.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A randomisation list will be generated prior to the study using computer software.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
3/09/2009
Actual
3/09/2009
Date of last participant enrolment
Anticipated
1/12/2009
Actual
1/12/2009
Date of last data collection
Anticipated
Actual
Sample size
Target
120
Accrual to date
Final
141
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 237260 0
University
Name [1] 237260 0
School of Psychiatry, University of New South Wales at St Vincent's Hospital
Country [1] 237260 0
Australia
Primary sponsor type
University
Name
School of Psychiatry, University of New South Wales at St Vincent's Hospital
Address
299 Forbes Street Darlinghurst NSW2010
Country
Australia
Secondary sponsor category [1] 236746 0
None
Name [1] 236746 0
Address [1] 236746 0
Country [1] 236746 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 239362 0
St Vincent's Hospital Human Research Ethics Committee (HREC)
Ethics committee address [1] 239362 0
Ethics committee country [1] 239362 0
Australia
Date submitted for ethics approval [1] 239362 0
Approval date [1] 239362 0
29/04/2008
Ethics approval number [1] 239362 0
HREC08/SVH/36

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 29846 0
Prof Nick Titov
Address 29846 0
Department of Psychology
Macquarie University
NSW 2109
Country 29846 0
Australia
Phone 29846 0
61 2 9850 9901
Fax 29846 0
Email 29846 0
[email protected]
Contact person for public queries
Name 13093 0
Professor Gavin Andrews
Address 13093 0
299 Forbes Street
Darlinghurst
NSW2010
Country 13093 0
Australia
Phone 13093 0
612 8382 1726
Fax 13093 0
612 8382 1721
Email 13093 0
[email protected]
Contact person for scientific queries
Name 4021 0
Professor Gavin Andrews
Address 4021 0
299 Forbes Street
Darlinghurst
NSW2010
Country 4021 0
Australia
Phone 4021 0
612 8382 1726
Fax 4021 0
612 8382 1721
Email 4021 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
Dimensions AIInternet Treatment for Depression: A Randomized Controlled Trial Comparing Clinician vs. Technician Assistance2010https://doi.org/10.1371/journal.pone.0010939
N.B. These documents automatically identified may not have been verified by the study sponsor.